key: cord-0024809-57ut9ahq
authors: Moreira, Vanessa; Leiguez, Elbio; Janovits, Priscila Motta; Maia-Marques, Rodrigo; Fernandes, Cristina Maria; Teixeira, Catarina
title: Inflammatory Effects of Bothrops Phospholipases A(2): Mechanisms Involved in Biosynthesis of Lipid Mediators and Lipid Accumulation
date: 2021-12-04
journal: Toxins (Basel)
DOI: 10.3390/toxins13120868
sha: 192eff0b87e027cb56e53744e8450c5a26fbff09
doc_id: 24809
cord_uid: 57ut9ahq

Phospholipases A(2)s (PLA(2)s) constitute one of the major protein groups present in the venoms of viperid and crotalid snakes. Snake venom PLA(2)s (svPLA(2)s) exhibit a remarkable functional diversity, as they have been described to induce a myriad of toxic effects. Local inflammation is an important characteristic of snakebite envenomation inflicted by viperid and crotalid species and diverse svPLA(2)s have been studied for their proinflammatory properties. Moreover, based on their molecular, structural, and functional properties, the viperid svPLA(2)s are classified into the group IIA secreted PLA(2)s, which encompasses mammalian inflammatory sPLA(2)s. Thus, research on svPLA(2)s has attained paramount importance for better understanding the role of this class of enzymes in snake envenomation and the participation of GIIA sPLA(2)s in pathophysiological conditions and for the development of new therapeutic agents. In this review, we highlight studies that have identified the inflammatory activities of svPLA(2)s, in particular, those from Bothrops genus snakes, which are major medically important snakes in Latin America, and we describe recent advances in our collective understanding of the mechanisms underlying their inflammatory effects. We also discuss studies that dissect the action of these venom enzymes in inflammatory cells focusing on molecular mechanisms and signaling pathways involved in the biosynthesis of lipid mediators and lipid accumulation in immunocompetent cells.

Bothrops spp. snakes are responsible for the majority of snakebites in Latin America. Envenomation by these snakes induces severe pathological alterations at the site of venom injection, characterized by an intense local inflammatory reaction associated with myonecrosis, pain, and hemorrhage, potentially leading to permanent tissue damage and disability [1] [2] [3] [4] [5] [6] . The local inflammatory response to bothropic envenomation involves a set of events including an increase in vascular permeability, edema formation, hyperalgesia, the activation and infiltration of immunocompetent cells, and a complex network of inflammatory mediators driving the inflammatory response [2] . These events are caused by the activation of critical host defense mechanisms of the victims by direct and indirect actions of

Phospholipases A 2 constitute a group of enzymes with diverse biological functions, ranging from homeostasis and membrane remodeling to the generation of metabolites and second messengers involved in biological processes and signal transduction. These enzymes hydrolyze the acyl ester bond at the sn-2 position of phospholipids, generating free fatty acids, such as arachidonic acid (AA) and oleic acid, and lysophospholipids, such as lyso-PAF [21, 22] . Currently, PLA 2 s are classified into close families, including secretory PLA 2 (sPLA 2 ), cytosolic phospholipase (cPLA 2 ), and Ca 2+ -independent PLA 2 (iPLA 2 ); platelet activating factor acetylhydrolase (PAF); and lysosomal PLA 2 (LPLA 2 ), PLA/acyltransferase (PLAAT), α/β hydrolase (ABHD), adipose-PLA 2 (AdPLA), and glycosylphosphatidylinositol (GPI)-specific PLA 2 [23] [24] [25] . This classification of PLA 2 s is based on the cell location, amino acid sequence, molecular weight, presence of intramolecular disulfide bridges, calcium requirement, and catalytic activity, including the hydrolysis at the sn-2 position of glycerophospholipids [22, 26] . The sPLA 2 family is largely distributed in nature, and its components are classified into I, II, III, V, IX, X, XI, XII, XIII, and XIV groups. They are present in high concentrations in snake, bee, and wasp venoms and in several mammalian organs, cells, and pancreatic juice [21, 27] . Among them, we highlight group I PLA 2 s, comprising the secreted enzymes found in the snake venoms of the Elapidae and Hydrophiidae families and in the pancreas secretion of mammals. Meanwhile, group II consists of sPLA 2 s found in snake venoms of the Viperidae family and in mammalian tissues and are expressed in inflammatory processes [13, 28] .

For a long time, the pathophysiological activities of sPLA 2 s were related exclusively to their enzymatic activity, capable of providing a substrate for the synthesis of second messengers and inflammatory mediators. However, alternative mechanisms of action have been associated with the ability of sPLA 2 to interact with receptors or even specific domains present on cell membrane surfaces, such as heparan sulfate proteoglycans, which have already been described to be important for triggering the activation of other sPLA 2 s in the target cells [29] [30] [31] [32] . The identification of sPLA 2 s binding proteins was initially achieved by Lambeau et al. (1989) [33] , who used the sPLA 2 from the Oxyuranus scutelatus snake venom, called OS2. Due to its prevalence in brain tissue, this protein was denominated an N (neuronal) type receptor. Then, through screening in various tissues and cells, for studies Toxins 2021, 13, 868 3 of 28 of other OS2 binding proteins, a second type of PLA 2 receptor was described, present in rabbit skeletal muscles, called an M (muscle) type receptor [34] . The presence of this latter receptor was identified in several tissues and in neutrophils, monocytes, and human alveolar macrophages [35, 36] , but not in murine peritoneal macrophages [37] . The M-type phospholipase A 2 receptor has a high degree of homology (~30%) to mannose receptors, a member of the lectin receptor family, constitutively expressed in macrophages [38, 39] . Mannose receptors are involved in phagocytosis, antigen processing [29, 38, 40] , and the production of inflammatory cytokines by macrophages [40] [41] [42] . Additionally, this receptor has been demonstrated to play a role in cell proliferation and AA release, via MAPKs (protein kinase activated by the mitogens family), induced by the group IB sPLA 2 s [43] [44] [45] . Furthermore, it has been revealed that group IIA sPLA 2 s can bind to mannose receptors and promote the release of IL-6 by human alveolar macrophages [46] .

Investigations into the biological role of mammalian group IIA PLA 2 , also known as inflammatory PLA 2 , in the development of several pathologies of inflammatory and immunological origin have been described. Several studies have revealed that group IIA sPLA 2 s are present in high levels in rheumatoid arthritis [47] [48] [49] [50] , acute pancreatitis [51] [52] [53] , septic shock [54, 55] , Crohn's disease and ulcerative colitis [56] [57] [58] , respiratory distress syndrome [59] [60] [61] , bronchial asthma and allergic rhinitis [59, 62] , atherosclerosis [63, 64] , autoimmune diseases [65] , and cancer [66] [67] [68] [69] . These observations imply that both local and systemic inflammation are associated with the release of sPLA 2 s in vivo, thus raising the unclear question of the role of these PLA 2 s in inflammatory reactions. Additionally, it was found that proinflammatory cytokines, such as interleukin (IL)-1β, IL-6, and tumor necrosis factor alpha (TNF-α), induce, in a variety of tissues, the gene transcription of sPLA 2 s and the subsequent increase in their secretion, thus, supporting the hypothesis of the involvement of sPLA 2 s in inflammation [70] [71] [72] [73] . In addition, sPLA 2 s activate intracellular signaling events in cells that participate in inflammatory processes, caused by the generation of second messengers, and the phosphorylation of kinases as of MAPK [74] [75] [76] [77] . Thus, sPLA 2 s represent an important target for investigations regarding the mechanisms of inflammatory events.

Inflammation is a response of body tissues to noxious conditions for restoring homeostasis, setting the stage for the healing and reconstitution of injured tissue. The acute inflammatory response to injury involves functional alterations of microvessels that occur early after injury and develop at varying rates. The major features of these alterations include transient vasoconstriction, followed by vasodilation, then, leakage of protein-rich fluid from the microcirculation leading to edema formation, and movement of phagocytic leukocytes into the site of injury followed by local pain [78] . Immunocompetent cells, such as neutrophils and monocytes, found in blood circulation are capable of rapidly infiltrating tissues; macrophages and dendritic cells reside within tissue and play key roles in tissue surveillance and antigen presentation [79, 80] . The vascular and cellular reactions are triggered and highly regulated by chemical factors, called inflammatory mediators, which include cytokines, chemokines, vasoactive amines, and eicosanoids and are produced by plasma components or are released in close proximity to the injury by endothelial cells, tissue-resident leukocytes such as mast cells, and macrophages at the early stages, followed by infiltrated leukocytes. The effects of inflammatory mediators involve the engagement of specific receptors, which then display signaling pathways responsible for the immune response [81] [82] [83] . Parallel to changes in blood flow, the margination of leukocytes begins, and leukocytes adhere to the microvascular endothelium through rolling and firm adhesion, and then moving through the vascular wall into the interstitial tissue. The various steps in the leukocyte migration are regulated by different subsets of cell-adhesion molecules expressed by both leukocyte and endothelial cells [84, 85] . Thereafter, the phagocytosis of offending agents by migrated leukocytes occurs, followed by a release of lysosomal enzymes and an increase in the oxidative metabolism in leukocytes, known as respiratory burst, [86, 87] . Four major classes of receptor-mediated phagocytosis exist: receptors of complement that recognize complement-coated particles; Fcg receptors, which are constitutively active for phagocytosis of IgG-coated particles; mannose receptors that recognize mannose and fucose on the surface of pathogens; and β-glucan receptors that recognize β-glucans-bearing ligands [87] . Furthermore, receptors for the Fc portion of immunoglobulin G and mannose/fucose residues lead to the release of proinflammatory mediators and reactive oxygen [88] .

Despite the stereotyped features associated with an inflammatory response, the signal pathways involved in this response are determined by the nature of the inflammatory trigger, the sensors that detect them, the inflammatory mediators released, and the tissue affected. A number of surface and cytosolic receptors expressed in innate immune cells can sense pathogen-associated molecular patterns (PAMPs), damage-associated molecular patterns (DAMPs), or venom-associated molecular patterns (VAMPs) with high sensitivity and specificity. The recognition of these molecules is achieved by interacting with pattern recognition receptors (PRRs) [89] . These sensing receptors include Toll-like receptors (TLRs) [90, 91] , C-type lectin receptors (CLRS), RIG-I-like receptors (RLRs), and nucleotidebinding domain leucine-rich repeat (NLRs) or nucleotide-binding and oligomerisation domain (NOD)-like receptors [92, 93] . Among them, TLRs (TLR1-TLR10) are highly conserved transmembrane proteins that play an important role in recognizing microbial pathogens and endogenous damage molecules, thereby triggering the generation of signals for the production of proinflammatory proteins and cytokines, via cooperation of adaptor proteins (MyD88, TIRAP, TRIF, and TRAM) [94, 95] . The recognition of specific molecular patterns by NLRs induces the oligomerisation of proteins in the cytosol, generating platforms called inflammasomes [96] . The inflammasome is a high molecular weight protein complex that elicits the activation of inflammatory caspases and the processing of pro-interleukin-1β (pro-IL-1β) and pro-IL-18, generating the mature biologically active cytokines and a rapid inflammatory form of cell death termed pyroptosis [97] . Several distinct inflammasomes have been identified, including NLR and the pyrin domain containing receptor 1 (NLRP1), NLRP3, and NLR; the caspase recruitment domain containing receptor 4 (NLRC4); and the AIM2-like receptors (ALR) family [98, 99] . These receptors positively regulate genes related to inflammatory mediators, including cytokines and key enzymes in the biosynthetic pathways of lipid mediators known as eicosanoids [100] .

The early induction of most inflammatory transcripts depends on networks of transcription factors whose activation is coupled to pathways of signal transduction. The nuclear factor-kappa B (NF-κB) is a major and the best-studied transcription factor of inflammatory response [101, 102] . The binding of activated NF-κB to the nuclear promoter region of diverse inflammatory factors leads to the transcriptional activation and expression of inflammatory mediators and enzymes. Currently, the major signaling pathways involved in inflammation are mediated by the cascade phosphorylation of protein kinases, such as the mitogen activated kinases (MAPKs) encompassing ERK1/2, SAPK, c-Jun NH2-terminal or JNK and p38MAPKs, phosphatidylinositol 3 kinase (PI3K), protein kinase C (PKC), and protein tyrosine kinase (PTK). These kinases mediate distinct intracellular signaling pathways associated with cytokines production, cytokine receptors, growth factors, mobilization of intracellular Ca 2+ , and regulate a variety of functions of immunocompetent cells, including cell migration, phagocytosis, degranulation, respiratory burst, and programmed cell death [103] [104] [105] [106] [107] [108] [109] [110] [111] [112] .

An effective acute inflammatory response results in the removal of noxious factors followed by the resolution and repair stages [113] . The shift in inflammatory markers, including the switch from proinflammatory mediators to anti-inflammatory, resolutioninducing mediators (lipoxins, maresins, protectins, and resolvins), is vital for the change from inflammation to resolution [114] . This switch drives the transition from neutrophil to monocyte recruitment into the affected sites, resulting in the clearance of dead cells and other debris, assisted by the lymphatic system, and the initiation of tissue repair at Toxins 2021, 13, 868 5 of 28 the damaged site [115] . However, if the acute events are not properly controlled, the inflammatory response becomes detrimental to the host. Yet, if the acute response does not succeed in neutralizing the injurious stimulus, the resolution phase might not be appropriately induced, and a chronic inflammatory state may ensue, leading to several inflammatory-mediated diseases [116, 117] . Phospholipases A 2 of GIIA are major components of Bothrops spp. snake venoms and play important roles in the pathophysiology of envenoming by these snakes, including the inflammatory response. Although these enzymes conserve a chemistry and catalytic structure, the natural evolution of viperid venoms introduced alterations in their primary amino acid residues, generating various other biological and toxicological effects [118] . In general, the GIIA sPLA 2 s found in viperid snake venoms are classified as sPLA 2 s, known as 'classic', containing an amino acid aspartate at position 49 (Asp49) and catalyzing the hydrolysis of the ester bond at position sn-2 of glycerophospholipids in a Ca 2+ dependent manner. Meanwhile, the other type of sPLA 2 s is described as 'variant' and contains a lysine at the same position 49 (Lys49), with or without low catalytic activity [119] . Such a substitution affects the ability of these proteins to bind to Ca 2+ , an essential cofactor for the stabilization of tetrahedral intermediate, which occurs in the catalytic reaction performed by the Asp49-sPLA 2 s [120] . Despite the lack of enzymatic activity, sPLA 2 s-Lys49 homologues maintain their damaging capacity in membranes through a mechanism that is not completely understood and independent of Ca 2+ [12, 121, 122] .

It has long been demonstrated that viperid sPLA 2 s are potent inductors of inflammation. Although they present differences in their catalytic activity, both viperid Asp49 and Lys49 PLA 2 homologues are capable of inducing local inflammation in diverse experimental models [123] [124] [125] . As such, this group of enzymes is considered to be a major component responsible for the severe local edema in envenomings by Bothrops spp. The inflammatory response to venom PLA 2 s is characterized by edema and the marked infiltration of leukocytes into the site of toxin injection. Studies on the mechanism of local edema induced by viperid sPLA 2 s (svPLA 2 s) have demonstrated an early increase in vascular permeability and a local release of inflammatory mediators, which act synergistically to cause the initiation and development of the inflammatory events. Among these mediators are vasoactive amines, including histamine, serotonin, and substance P, as well as vasodilating prostaglandins. Yet, in vivo studies employing a pharmacological approach have demonstrated that antagonists of serotonin and H1 receptors of histamine reduced the progression of edema induced by both catalytically active and inactive variants of sPLA 2 isolated from B. asper [126] , B. neuwiedii [127] , B. jararacussu [128, 129] , or B. insularis [130] . In support of these reports, the release of histamine and serotonin by mast cells was observed following stimulation with bothropic sPLA 2 s from B. jararacussu [128, 131] . Consistent with this evidence, the contribution of mast cells to edema formation induced by viperid PLA 2 s was further observed in in vitro experimental models demonstrating the ability of sPLA 2 s isolated from B. pirajai, B. jararacussu, and B. atrox snake venoms to degranulate mast cells [125, 128, 131, 132] . It is well known that upon activation, mast cells secrete and synthesize an array of inflammatory mediators, which trigger the earliest events of inflammation [133, 134] . Moreover, the contribution of the catalytic activity for the edematogenic effect of the enzymatic active Asp49 from bothropic PLA 2 s was suggested by studies, revealing that the chemical modification of this sPLA 2 by p-bromophenacyl bromide inhibited edema formation induced by these viperid PLA 2 s [126] [127] [128] . In addition, the role of lipid mediators, such as PAF and eicosanoids, for hyperalgesia induced by catalytic active venom PLA 2 s was highlighted by studies using a pharmacological approach [135] . These authors suggested that the enzymatic hydrolysis of membrane phospholipids played a role in these events by directly releasing the precursors of lipid mediators, such as lyso-PAF and AA.

As mentioned previously, leukocytes are central components of inflammation. An important cellular component exists in the inflammatory response to Bothrops sPLA 2 s. As such, the stimulatory effect of piratoxin-I, bothropstoxin-I, and -II from B. pirajai and B. jararacussu, respectively, on neutrophil chemotaxis was demonstrated in an in vitro experimental model [136] . This effect was revealed to involve the interaction of these sPLA 2 s with surface heparan binding sites of neutrophils, followed by the release of chemotactic mediator leukotriene B 4 (LTB 4 ) and PAF, and is independent of enzyme activity. Furthermore, the ability of these venom PLA 2 s to recruit an endogenous PLA 2 through the activation of GTP-binding protein and PKC was added to the mechanisms by which they cause neutrophil migration [137] . Moreover, studies conducted using in vivo experimental models have demonstrated the ability of Bothrops sPLA 2 s to induce a marked influx of polymorphonuclear and mononuclear cells into the site of their injection, as demonstrated for both catalytic active and non-catalytic venom PLA 2 s, such as MT-III and MT-II from B. asper snake venom [123, 138] . A similar effect was reported by other authors, investigating various sPLA 2 s isolated from different Bothrops spp. snake venoms, such as Bothropstoxin (BthTX)-I and BthTX-II; B. jararacussu [131] , BnSP-7, a catalytically inactive PLA 2 from B. pauloensis [139] , BatroxPLA 2 from B. atrox [140] and BJ-PLA 2 -I from B. jararaca [141] in in vivo experimental models. The sPLA 2 -induced leukocyte migration was linked to the upregulation of adhesion molecules, such as l-selectin, LFA-1, and CD18, which in turn was associated with the release of inflammatory cytokines IL-1β, IL-6, and TNF-α with chemotactic activity by resident leukocytes, primarily macrophages [123] . Cytokines, chemokines, and leukotriene B 4 are among the major mediators regulating the expression of adhesion molecules and chemotaxis of leukocytes [142] [143] [144] . Consistent with this information, increased serum levels of IL-6, IL-1, and TNF-α induced by Bbil-TX from B. bilineata snake venom were observed in a mouse experimental model [145] . In addition, there are reports that two Lys49 PLA 2 s isolated from B. mattogrossensis (BmaTX-I and BmaTX-II) venom were able to induce the release of IL-1β by murine neutrophils in culture [146] and that BatroxPLA 2 , an acidic sPLA 2 from B. atrox venom, induced the release of IL-6, PGE 2 , and LTB 4 from murine macrophages in culture [140] . In this context, the involvement of inflammasomes in the production of IL-1β induced by Bothrops sPLA 2 s was recently investigated. The participation of NLP3 inflammasome via the activation of caspase 1 in the production of IL-1β induced by BthTX-I, a Lys49-PLA 2 from B. jararacussu venom, injected into mouse gastrocnemius muscle was reported [147] . In addition, the participation of inflammasomes in BthTX-I-induced production of IL-1β was demonstrated in peritoneal macrophages. This effect was demonstrated to be dependent on caspase 1/11, ASC, and NLRP3 and was associated with the release of ATP and activation of P2X7 receptors [148] . Despite the importance of cytokines, chemokines, and eicosanoids in orchestrating the events of inflammation and the potent proinflammatory effects triggered by viperid sPLA 2 s, including those from Bothrops genus, a complete picture of the inflammatory mediators released by immunocompetent cells upon stimulus by Bothrops sPLA 2 s has yet to be further investigated. Moreover, the mechanisms involved in the production and release of these mediators and the possible crosstalk between them remain to be better clarified. Regarding the mechanisms involved in the biosynthesis of lipid mediators induced by Bothrops sPLA 2 s, the progress made is presented in this review as a separate item (Section 2.2).

It is well recognized that the activation of innate effector functions, such as phagocytosis, and the production of microbicidal substances in leukocytes are critical for host defense and tissue repair. Regarding phagocytosis, studies have demonstrated the activity of Bothrops sPLA 2 s to induce phagocytosis following the activation of distinct receptors in immune-competent cells. In this sense, it was demonstrated that MT-II and MT-III, isolated from B. asper snake venom, can directly stimulate phagocytosis by macrophages in culture. MT-II significantly increased phagocytosis mediated by all classes of receptors, whereas MT-III increased phagocytosis via only mannose and beta-glucan receptors. This suggests that although the catalytic activity of Bothrops sPLA 2 s is not an essential requirement for enhancing macrophage phagocytosis, it may drive the class of phago-Toxins 2021, 13, 868 7 of 28 cytosis receptors involved in this process. Molecular regions distinct from the catalytic network are likely involved in this effect [138] . In addition, the signaling pathways mediating zymosan phagocytosis, induced by both MT-II and MT-III, were investigated, with a focus on lipid second messengers. This study demonstrated that whereas the effect of MT-III, catalytically active, was dependent on the activation of endogenous iPLA 2 , the effect of MT-II was dependent on both endogenous iPLA 2 and cPLA 2 . Likewise, COX-2 and 5-LO-derived metabolites in addition to PAF were involved in the signaling events required for phagocytosis induced by both venom sPLA 2 s [138] . In line with these data, BaltTX-I, devoid of catalytic activity and isolated from B. alternatus snake venom, was reported to activate the phagocytosis of serum-opsonized zymosan by murine macrophages, indicating the involvement of complement receptors. In addition, the participation of PKC was demonstrated. Nonetheless, BaltTX-II, a catalytically active sPLA 2 isolated from the same venom did not stimulate phagocytosis in macrophages, lending support to previous findings that the catalytic activity of Bothrops sPLA 2 s is not essential for the stimulation of phagocytosis via complement receptor [149] . In addition, the sPLA 2 s isolated from Panamanian B. asper snake venom, pMTX-III (catalytically active Asp49) and pMTX-II and -IV, two enzymatically inactive Lys49 isoforms, were described to induce phagocytosis via mannose receptor and superoxide production in macrophages [150] . The mechanisms underlying the differences between the catalytic and non-catalytic active Bothrops PLA 2 s, regarding the activation of phagocytosis in macrophages and the participation of distinct receptors in their effects, require further clarification.

Concomitantly with phagocytosis, there is an increase in the oxidative metabolism, also referred to as respiratory burst, in leukocytes. In this context, the literature reveals that viperid sPLA 2 s can trigger the respiratory burst in immunocompetent cells. In the first study describing the ability of Bothrops sPLA 2 to induce the release of microbicidal agents, the authors demonstrated that MT-II and MT-III, isolated from B. asper snake venom, induced the release of H 2 O 2 by macrophages, with MT-III being the more potent stimulator [151] . In agreement with this evidence, it has been demonstrated that BaltTX-I and BaltTX-II from B. alternatus snake venom induced superoxide production by macrophages in culture in a process mediated by PKC [149] . In addition, other authors have revealed that the three sPLA 2 s from B. atrox venom, namely BaTX-I, a Lys49 variant devoid of catalytic activity; BaTX-II, a catalytically active Asp49; and BaPLA 2 , an acidic Asp49 sPLA 2 induced the release of the superoxide anion by the J774A.1 lineage macrophages in culture [152] . BaTX-I was the only sPLA 2 able to stimulate complement receptor-mediated phagocytosis, but all studied sPLA 2 s could increase the macrophage lysosomal volume [152] . These data demonstrate the ability of Bothrops PLA 2 s to trigger the respiratory burst, which is an essential process for the elimination of harmful agents. Although the structural determinants of such an effect were not investigated, it is likely that neither the enzymatic activity nor the basic or acidic characteristic of PLA 2 is essential for the activation of the respiratory burst.

An additional defensive strategy important for host defense is the neutrophil extracellular trap, or 'NET'. The formation of NET (NETosis) occurs through the release of nuclear DNA, forming a sticky 'net' of extracellular fibers that can halt the dissemination of pathogens and toxins [153, 154] . Despite its importance in the inflammatory response, little attention has been paid to the involvement of this defense mechanism in the effects of viperid sPLA 2 s. Yet, a report indicates that BaTX-II, an Asp49 PLA 2 isolated from B. atrox snake venom, can activate human neutrophils in culture to produce hydrogen peroxide via the PI3K signaling pathway. Furthermore, this sPLA 2 stimulated neutrophils to secrete MPO, NETs, and inflammatory mediators, including IL-1β, IL-8, and LTB 4 [155] . Therefore, the activation of neutrophilic functions, including toxin trapping and inactivation, is likewise involved in the inflammatory response to Bothrops sPLA 2 s. Further studies are necessary to amplify the knowledge regarding the participation of NETs in inflammation induced by Bothrops spp. sPLA 2 s. Interestingly, in contrast to the reported ability of Bothrops sPLA 2 s to activate distinct inflammatory functions in leukocytes, a report revealed that CB (Crotoxin B), a catalytically active sPLA 2 isolated from Crotalus durissus terrificus, which is a subunit of crotoxin complex [156, 157] , could, per se, display inhibitory effects in macrophage functions, including spreading and phagocytosis [158] . Such an inhibitory effect suggests an anti-inflammatory activity for this particular viperid sPLA 2 [159] . In agreement with this idea, CB was reported to reduce the release of inflammatory cytokines, including IL-6 and TNF-α, and increase the release of PGE 2 and lipoxin A4, both immunomodulatory lipid mediators, in dendritic cells [160] . A summary of the inflammatory activities of svPLA 2 s is illustrated in Figure 1 . In Table 1 , the svPLA 2 s-induced inflammatory responses are summarized according to the amino acid residue at position 49 and basic and acidic characteristics. stimulated neutrophils to secrete MPO, NETs, and inflammatory mediators, including IL-1β, IL-8, and LTB4 [155] . Therefore, the activation of neutrophilic functions, including toxin trapping and inactivation, is likewise involved in the inflammatory response to Bothrops sPLA2s. Further studies are necessary to amplify the knowledge regarding the participation of NETs in inflammation induced by Bothrops spp. sPLA2s. Interestingly, in contrast to the reported ability of Bothrops sPLA2s to activate distinct inflammatory functions in leukocytes, a report revealed that CB (Crotoxin B), a catalytically active sPLA2 isolated from Crotalus durissus terrificus, which is a subunit of crotoxin complex [156, 157] , could, per se, display inhibitory effects in macrophage functions, including spreading and phagocytosis [158] . Such an inhibitory effect suggests an anti-inflammatory activity for this particular viperid sPLA2 [159] . In agreement with this idea, CB was reported to reduce the release of inflammatory cytokines, including IL-6 and TNF-α, and increase the release of PGE2 and lipoxin A4, both immunomodulatory lipid mediators, in dendritic cells [160] . A summary of the inflammatory activities of svPLA2s is illustrated in Figure 1 . In Table 1 , the svPLA2s-induced inflammatory responses are summarized according to the amino acid residue at position 49 and basic and acidic characteristics. Figure 1 . Scheme of inflammatory activities of svPLA2s. The svPLA2s induce inflammatory events, characterized by activation of innate immune cells and endothelial cells and release of several inflammatory mediators that interfere in the vascular dynamic. svPLA2s induce mast cells degranulation and activation of resident macrophages with release of inflammatory mediators such as prostaglandins (PGs), histamine, serotonin, and substance P, which lead to vasodilation, increase of vascular permeability, culminating in edema formation and pain. In addition, svPLA2s activate phagocytosis Figure 1 . Scheme of inflammatory activities of svPLA 2 s. The svPLA 2 s induce inflammatory events, characterized by activation of innate immune cells and endothelial cells and release of several inflammatory mediators that interfere in the vascular dynamic. svPLA 2 s induce mast cells degranulation and activation of resident macrophages with release of inflammatory mediators such as prostaglandins (PGs), histamine, serotonin, and substance P, which lead to vasodilation, increase of vascular permeability, culminating in edema formation and pain. In addition, svPLA 2 s activate phagocytosis by macrophages and increase the local production of oxygen reactive species (ROS). Furthermore, svPLA 2 s, along with vascular alterations and produced inflammatory mediators, increase the expression of adhesion molecules such as LFA, CD-18 and L-selectin. These adhesion molecules, in turn, promote chemotaxis and leukocyte migration. The svPLA 2 s induce production of myeloperoxidase (MPO) and release of NETs by neutrophils. Both neutrophils and macrophages release proinflammatory mediators such as platelet-activating factor (PAF), IL-8, LTB 4 , IL-1β, IL-6, and TNF-α. These last three mediators are involved in the upregulation of COX-2 isoform, and release of PGs, thus amplifying the inflammatory response induced by svPLA 2 s. Phagocytosis, superoxide production (in vitro) [149] BaltTX-II B. alternatus Basic Asp49

Superoxide production (in vitro) [149] pMTX-II B. asper Basic Lys49

Phagocytosis, superoxide production (in vitro) [150] pMTX-III B. asper Basic Asp49 Phagocytosis, superoxide production (in vitro) [150] pMTX-IV B. asper Basic Lys49

Phagocytosis, superoxide production (in vitro) [150] BaTX-I B. atrox Basic Lys49 Superoxide production, lipid droplet formation (in vitro) [155] [132] nd, not described.

It is well established that sPLA 2 s play key modulatory roles in numerous cellular processes in physiological and pathological conditions by regulating the release of AA from membrane phospholipids [27, 171] . It has long been recognized that the AA-derived lipid mediators are potent mediators of inflammation [83] . The AA is rapidly metabolized by several enzyme complexes, including cyclooxygenases (COX), lipoxygenases (LOX), and cytochrome P450 (CYP450). These enzymatic pathways promote the synthesis of oxygenated and bioactive products, generically called eicosanoids, which include prostaglandins (PG), leukotrienes (LT), hydroperoxyeicosatetraenoic acids (HPETEs), hydroxyeicosatetraenoic acids (HETEs), epoxides (EETs), and lipoxins (LX) [172] [173] [174] [175] [176] [177] [178] . A summary of the cascades involved in biosynthesis of eicosanoids is shown in Figure 2 .

It is important to emphasize that COX-1 is a constitutive isoform present in most tissues and is responsible for generating PGs for diverse physiological functions [179] [180] [181] [182] . In contrast, COX-2 is upregulated by inflammatory cytokines and growth factors [183, 184] and is constitutively expressed in some tissues [185, 186] .

Regarding the production of inflammatory eicosanoids by Bothrops svPLA 2 , studies have demonstrated that the intraperitoneal injection of MT-III [187] and MT-II [162] in mice induced an early and transient release of PGD 2 , followed by a rapid and sustained release of PGE 2 . Likewise, in mice injected with BatroxPLA 2 [140] , from B. atrox snake venom, and BJ-PLA 2 -I from B. jararaca [141] , an early release of PGE 2 was observed. The in vivo experimental models of previous studies have revealed that B. asper sPLA 2 s induce the release of other eicosanoids, such as thromboxane A 2 (TXA 2 ) and LTB 4 [123] . Moreover, an Asp49 svPLA 2 from B. atrox venom [140] stimulated the production of LTB 4 , lipoxin, and PGE 2 . PGE 2 and PGD 2 are important modulators of vasodilation, and PGE 2 can potentiate an increase in vascular permeability, promoted by mediators of this phenomenon, with a consequent formation of edema [188, 189] . Studies using pharmacological treatment with non-steroidal anti-inflammatory compounds were crucial in demonstrating the participation of these COXs-derived lipid mediators on edema [126, 190] and hyperalgesia [135] , induced by B. asper sPLA 2 s. In addition, studies demonstrating that MT-III and MT-II upregulated COX-2 protein expression in peritoneal leukocytes without altering the constitutive expression of COX-1 evidenced the ability of these venom PLA 2 s to influence downstream cyclooxygenase isozymes and suggested this as a mechanism by which these sPLA 2 s induced the production of prostaglandins [162, 163] . Moreover, these findings suggested that the catalytic activity of these bothropic PLA 2 s did not contribute to the induction of PG biosynthesis, since MT-II, devoid of catalytic activity, caused the same effect.

In this regard, studies have demonstrated that the IκB phosphorylation inhibitor TPCK effectively prevented both MT-II-or MT-III-induced COX-2 expression, suggesting that the activation of NF-κB was critical for the induction of COX-2 expression by these bothropic svPLA 2 s. The involvement of NF-κB as the mechanism underlying this venom sPLA 2 sinduced upregulation of COX-2 expression was further confirmed by results that revealed the inhibition of the NF-κB nuclear translocation site, markedly reduced svPLA 2 s-induced COX-2 expression and, as a consequence, reduced PGE 2 production by macrophages in culture [162, 164] . It is important to emphasize that COX-1 is a constitutive isoform present in most tissues and is responsible for generating PGs for diverse physiological functions [179] [180] [181] [182] . In contrast, COX-2 is upregulated by inflammatory cytokines and growth factors [183, 184] and is constitutively expressed in some tissues [185, 186] .

Regarding the production of inflammatory eicosanoids by Bothrops svPLA2, studies have demonstrated that the intraperitoneal injection of MT-III [187] and MT-II [162] in mice induced an early and transient release of PGD2, followed by a rapid and sustained release of PGE2. Likewise, in mice injected with BatroxPLA2 [140] , from B. atrox snake venom, and BJ-PLA2-I from B. jararaca [141] , an early release of PGE2 was observed. The in vivo experimental models of previous studies have revealed that B. asper sPLA2s induce the release of other eicosanoids, such as thromboxane A2 (TXA2) and LTB4 [123] . Moreover, an Asp49 svPLA2 from B. atrox venom [140] stimulated the production of LTB4, lipoxin, and PGE2.

PGE2 and PGD2 are important modulators of vasodilation, and PGE2 can potentiate an increase in vascular permeability, promoted by mediators of this phenomenon, with a consequent formation of edema [188, 189] . Studies using pharmacological treatment with Studies employing mouse resident peritoneal macrophages or neutrophils in culture revealed that viperids sPLA 2 s induced a marked release of PGE 2 in cell supernatants, accompanied by the release of AA [162, 165, 166, 191] . These data support the results in vivo and serve as evidence that immune innate leukocytes, such as resident macrophages and neutrophils, are important sources of PGs under in vivo stimuli by sPLA 2 from Bothrops spp. snake venoms. Interestingly, studies have demonstrated that the incubation of resident peritoneal macrophages with MT-II or MT-III significantly increased the concentration of AA [162, 164] . Although the release of AA induced by the Asp49 sPLA 2 was approximately 20 times greater than that induced by MT-II, it demonstrated that the catalytic activity of viperid sPLA 2 s was not an essential requirement for inducing COX-2 expression and PGE 2 production. According to Kini and Evans (1995) [192] , in mechanisms independent on catalytic activity, as in the case of MT-II, the interaction of sPLA 2 s to acceptor regions can cause the biological effect or interfere with the interaction of target proteins with their physiological ligands. Furthermore, some effects may result from combinations of both enzymatic and non-enzymatic mechanisms [192] , leading to the activation of several signaling pathways; this should be considered when interpreting the effects of group IIA Lys49 svPLA 2 s. In this context, since crosstalk among sPLA 2 , cPLA 2 , and iPLA 2 s has been demonstrated to occur in several physiological and inflammatory conditions [193] [194] [195] [196] , the contribution of prey/victim cPLA 2 and/or iPLA 2 to the increased production of PGs and upregulation of COX-2 protein expression induced by svPLA 2 variants was evaluated in diverse in vitro experimental models [162, 165, 187] . Thus, the pharmacological treatment of cells with the cPLA 2 inhibitor but not the iPLA 2 inhibitor decreased the release of AA and the production of PGE 2 and PGD 2 induced by svPLA 2 . In contrast, these pretreatments did not modify the MT-III-induced COX-2 expression but reduced the COX-2 expression induced by MT-II. These results demonstrate that cPLA 2 is required for distinct actions of MT-II in the PG biosynthetic pathway in macrophages [162, 187] . This is consistent with the reported functional cooperation between intracellular PLA 2 s and GIIA sPLA 2 for PG biosynthetic responses in several other cell systems [171, [197] [198] [199] . The role of cPLA 2 as a key enzyme in supplying AA for COX-2-dependent PGs production is well established [171, 200, 201] . Taken together, the available data demonstrate that the Asp49 svPLA 2 s are functionally coupled with cPLA 2 , since prior activation of cPLA 2 is required for MT-III to act with downstream enzymes for PG biosynthesis in macrophages and neutrophils [165, 187] . Interestingly, the association of Lys49 sPLA 2 with cPLA 2 , in addition to being important for the supply of AA for the production of PG, appears to modulate the transcription and protein expression of COX-2 inflammatory isoform. The mechanisms involved in the coupling between the venom GIIA sPLA 2 s and mammalian cPLA 2 have yet to be investigated. One possibility is that GIIA svPLA 2 s activate cPLA 2 by distinct signaling cascades that mimic the transducing mechanism conveyed by physiological activators of cPLA 2 , such as MAPKs, since this enzyme family is likewise important for the activation of NF-κB [202] . In line with this concept, the Asp49 svPLA 2 , MT-III, in addition to Lys49 PLA 2 , MT-II, from B. asper snake venom, were revealed to stimulate the phosphorylation of protein kinases, including the MAPKs, such as p38MAPK and ERK1/2 [167, 169, 171] . Moreover, other protein kinases, including PI3K, PKC, and PTK, were reported to be phosphorylated in macrophages stimulated by both MT-III and MT-II [162, 164] . In this regard, studies have demonstrated that MT-III (Asp49 sPLA 2 ) stimulates PKC and p38MAPK pathways to positively modulate PGE 2 production and COX-2 expression via NF-κB, while MT-II (Lys49 PLA 2 ) displays similar effects by activating PKC, ERK1/2, and PTK in murine peritoneal macrophages [167, 169, 171] . Since PTK is involved in the activation of MAPKs, which, in turn, are essential for cPLA 2 activation, this signaling protein might be involved in the activation of cPLA 2 by MT-II [202] [203] [204] . Furthermore, another pathway implicated in the release of PGE 2 and the expression of COX-2 induced by MT-III was demonstrated to be independent of NF-κB activation. This pathway involved the activation of ERK1/2 by the 12-HETE pathway, the main product of 12-LO [166] . The involvement of another transcription factor in these MT-III-induced effects was suggested by the authors. Together, these findings reveal the variety and complexity of the mechanisms involved in the effects of svPLA 2 leading to the generation of lipid mediators. The signaling molecules and pathways acting in an innate immune cell (macrophage) upon stimulus either by Asp49 or Lys49 svPLA 2 are summarized in Figure 3 .

Although the participation of the M-type PLA 2 receptor or another type of interaction of Bothrops sPLA 2 with membrane sites for the stimulation of signal transduction pathways has not yet been demonstrated, a study revealed for the first time the involvement of the TLRs in the inflammatory response induced by MT-III (Asp49-PLA 2 ) from B. asper in macrophages [205] . The involvement of TLR2 and MyD88 adapter molecules was demonstrated to be critical in producing PGs, COX-2 protein expression, and cytokines IL-1β and IL-10 induced by this svPLA 2 . An indirect mechanism for the activation of TLRs through the release of DAMPs was suggested by the authors, since the analysis of the fatty acids released by the hydrolysis of membrane phospholipids by MT-III revealed high levels of oleic and palmitic acids. In this context, it is known that arachidonic, oleic, and palmitic acids produced by membrane cleavage by sPLA 2 s are important bioactive mediators involved in the induction and release of COX-2 and PGE 2 , respectively, through the activation of intracellular signaling mechanisms in several cell types [206] [207] [208] [209] .

demonstrated that MT-III (Asp49 sPLA2) stimulates PKC and p38MAPK pathways to positively modulate PGE2 production and COX-2 expression via NF-κB, while MT-II (Lys49 PLA2) displays similar effects by activating PKC, ERK1/2, and PTK in murine peritoneal macrophages [167, 169, 171] . Since PTK is involved in the activation of MAPKs, which, in turn, are essential for cPLA2 activation, this signaling protein might be involved in the activation of cPLA2 by MT-II [202] [203] [204] . Furthermore, another pathway implicated in the release of PGE2 and the expression of COX-2 induced by MT-III was demonstrated to be independent of NF-κB activation. This pathway involved the activation of ERK1/2 by the 12-HETE pathway, the main product of 12-LO [166] . The involvement of another transcription factor in these MT-III-induced effects was suggested by the authors. Together, these findings reveal the variety and complexity of the mechanisms involved in the effects of svPLA2 leading to the generation of lipid mediators. The signaling molecules and pathways acting in an innate immune cell (macrophage) upon stimulus either by Asp49 or Lys49 svPLA2 are summarized in Figure 3 . Free fatty acids can act as DAMPs and activate TLR2 or other TLRs (still unknown), via activation of adapter protein MyD88, leading to COX-2 protein expression and release of PGs, Asp49PLA 2 upregulates the 12-LO pathway, culminating the release of 12-HETE. 12-HETE, in turn, activates the ERK1/2 pathway, leading to COX-2 protein expression and PG release, independent on NF-κB translocation. Asp49PLA 2 also activates the signaling protein PI3K leading to COX-2 expression and production of PGs independent on NF-κB activation. Asp49 PLA 2 also activates PKC and p38 MAPK pathways promoting COX-2 expression and production of PGs via NF-κB activation. In addition, Asp49PLA 2 provides AA for activation of COX-1 activity which is followed by production of proinflammatory PGs. Asp49 and Lys49 PLA 2 s both produce PGs by pathways independent on iPLA 2 . Although both sPLA 2 from bothropic venom produce PGs via crosstalk with cPLA 2 , only Lys49PLA 2 induces COX-2 expression dependent on this cytosolic PLA 2 . Lys49PLA 2 activates signaling pathways mediated by p38 MAPK, PTK, PKC, and ERK1/2. All these kinase pathways, except for p38 MAPK, are involved in NF-κB activation and COX-2 protein expression and PG production. Full arrows indicate actions already studied and demonstrated. Dotted arrows indicate hypothesized or unknown effects.

As mentioned, the high enzymatic activity exhibited by ophidian sPLA 2 provides a microenvironment rich in free fatty acids that exert stimulating effects in immunocompetent cells, leading to the biosynthesis of lipid mediators. Moreover, excess free fatty acids exert cytotoxic effects that trigger the activation of cellular mechanisms capable of converting free fatty acids into metabolites of lower toxicity, known as neutral lipids (triacylglycerol and cholesterol-energetic body reserve) [210] . In recent decades, numerous studies have demonstrated the activation of intracellular metabolic pathways responsible for the metabolization of free fatty acids in neutral lipids and the consequent formation of dynamic organelles called lipid droplets (LDs) [211, 212] . These organelles are composed of a hydrophobic neutral lipid core surrounded by a phospholipid monolayer membrane, which contains numerous proteins related to cellular activation in addition to structural proteins, such as perilipin 2 (PLIN2), which plays an important role in LD assembly and the formation of foam macrophage [213] , marker cells in metabolic diseases, such as atherosclerosis and obesity [214] . LDs are commonly present in adipocytes due to the already-established role of these cells in the supply of energy in mammalian organisms [215] . In addition to the relevance regarding lipid homeostasis, the direct relationship between increased LD formation and inflammatory processes was evidenced by numerous studies [216] [217] [218] . In this sense, mammalian group IIA sPLA 2 s have been identified as potential plasma biomarkers for diseases related to lipid imbalance, such as atherosclerotic cardiovascular disease and obesity [219] . Alongside a marked inflammatory reaction, these metabolic diseases are characterized by lipid accumulation in immunocompetent cells [220, 221] . In line with the ability of svPLA 2 s to elicit an inflammatory response characterized by a high level of inflammatory mediators and free fatty acids, it was demonstrated that MT-III (Asp49 PLA 2 ), isolated from B. asper venom, induced LD formation enriched by PLIN2 protein in mice peritoneal macrophages [170] . This effect was likewise observed in rat vascular smooth muscle cells isolated from the thoracic aorta stimulated by MT-III [168] . Moreover, the ability of MT-II, a Lys49 PLA 2 homologue devoid of catalytic activity from B. asper venom, to directly activate macrophages to form LDs was reported [167] . This effect was reproduced by a synthetic peptide corresponding to the C-terminal sequence 115-129 of MT-II, evidencing the critical role of C-terminus for the MT-II-induced effect [167] . Similarly, BaTX-I, a catalytically inactive Lys49 variant; BaTX-II, a catalytically active Asp49; and BaPLA 2 , an acidic catalytically active Asp49 PLA 2 , isolated from B. atrox snake venom, increased the number of LDs on murine macrophages cell line J774A.1 [152] . The formation of LDs upon stimulus by MT-III was likewise demonstrated in human monocytes of peripheral blood [222] .

Considering the above information, LD formation induced by svPLA 2 s in phagocytes proved to be inherent to the action of sPLA 2 s regardless of the catalytic activity. The capability of Bothrops svPLA 2 s to induce the formation of LDs is related to the activation of PRRs of an innate immune response, kinase proteins, and intracellular PLA 2 signaling pathways involved in cellular metabolism, proliferation, and differentiation [170, 205] . Hence, by using gene knockout mice cells and a pharmacological approach, the participation of TLR2, MYD 88 adaptor protein, and CD36 in LD formation in macrophages in culture has been reported [170, 205] . In addition, the upregulation of CD36 receptors was observed in these cells. Considering the participation of the MYD 88 adaptor molecule, the involvement of other TLRs has yet to be investigated. In line with the reported Asp49 svPLA 2 action on PRRs, the upregulation of both SRA-1, from the scavenger receptor family, and LOX-1, an LDL receptor, was demonstrated in mouse aortic smooth muscle cells (VSMCs) [168] . These findings demonstrate that the inflammatory response elicited by Asp49 svPLA 2 likewise involved the upregulation of PRRs associated with lipid uptake in immunocompetent cells. This fact indicates that svPLA 2 s can be useful tools in studies aiming to understand the diseases associated with lipid imbalance.

In addition to providing the synthesis of mediators, TLR2 activation elicited by MT-III action was related to cytoskeleton activation [205] , a critical step in the transport of structural proteins into LDs, such as PLIN2. Cytoskeletal activation involves the activation of kinase proteins [223] . Consistent with this information, the participation of kinase proteins in LD formation induced by both Asp49 and Lys49 svPLA 2 s from B. asper venom has been demonstrated through a pharmacological approach and the detection of phosphorylated kinase proteins. Yet, MT-II-and MT-III-induced LD biogenesis is dependent on the ac-tivation of PKC, PI3K, p38MAPK, and ERK1/2 signaling pathways in mice peritoneal macrophages [224] . It is well known that PKC regulates a variety of processes associated with lipid droplet biology, such as adipocyte differentiation [225] , magnolol-induced lipolysis [226] , cholesterol-induced targeting of caveolin to lipid droplets [227] , and the expression of the PAT family [228] . Hence, the activation of the PKC signaling pathway in macrophages stimulated by the Bothrops PLA 2 s MT-II and MT-III in peritoneal macrophages may be implicated in an increase in PLIN2 protein expression, since LD formation induced by both svPLA 2 s has always been accompanied by an increase in PLIN2 protein expression in macrophages.

PI3K/AKT is a classical pathway involved in insulin resistance, cell growth, and lipid metabolism associated with the inhibition of cholesterol efflux leading to LD formation [229] . In this sense, the participation of the PIK3 signaling pathway in MT-III-induced LDs in macrophages and vascular smooth muscle cells stimulated with MT-III has been demonstrated [167, 224] . In the case of vascular smooth muscle cells, the activation of PI3K was related to the uptake of fatty acids to LDs by macropinocytosis [167] . Furthermore, the findings that MT-III increases phagocytic activity and upregulates macrophage markers in VSMCs reinforce the importance of this class of enzymes as inducers of factors implicated in the formation of foamy cells in both mononuclear phagocytic cells and VSMCs, which are key elements in the development of metabolic diseases.

The MAPK signaling pathway has been revealed to mediate the activation of intracellular PLA 2 s in physiologic and inflammatory contexts [230, 231] . It has been demonstrated that the ERK1/2 signaling pathway is implicated in LD formation via the activation of phospholipase D (PLD) and phosphorylation of dynein [232, 233] . Consistent with this information, the critical role of ERK1/2 for LD formation induced by MT-II and MT-III in macrophages and VSMCs was reported [167, 224] . Regarding p38 MAPK, the literature evidenced its importance in the development of atherosclerosis [234] and the apoptosis of foam macrophages. Macrophage death is a feature of atherosclerotic plaque linked to necrosis and plaque destabilization [235] . Interestingly, although MT-III has been demonstrated to activate apoptotic pathways, including the p38 MAPK signaling pathway, DGAT, ACAT, cPLA 2 , and LD formation in macrophages, no change in cell viability was observed. Further studies may clarify this lack of apoptotic effect.

It is known that the MAP kinases signaling pathway is implicated in intracellular PLA 2 activation, including the Ca 2+ -dependent cytosolic group IVA PLA 2 (cPLA 2α ) and the Ca 2+ -independent group VIA PLA 2 (iPLA 2 ) involved in both physiological and pathophysiological conditions [236, 237] . The biogenesis of LDs in CHO-K1 cells submitted to an enriched environment of fatty acids demonstrated ERK, p38, and JNK signaling pathway activation, with JNK cascade being responsible for cPLA 2α phosphorylation in this event. Of note, cPLA 2 was likewise implicated in LD biogenesis stimulated by MT-III associated with the activation of ERK and the p38 MAPK signaling pathway [224] . Considering the ability of cPLA 2 to mobilize cell membrane fatty acids [238] , the aforementioned activation should amplify the action of MT-III and provide a greater substrate for the metabolization and formation of LDs. Moreover, the biogenesis of LDs induced by the svPLA 2 s MT-III and MT-II is dependent on the activation of iPLA 2 signaling pathways [167, 224] . This signaling pathway was associated with the processing of fatty acids into triacylglycerol, a relevant component in the constitution of LDs [214] . Hence, the crosstalk already evidenced between intracellular PLA 2 and svPLA 2 to elicit inflammatory conditions [169] might contribute to elucidating mechanisms related to the formation of LDs.

The peroxisome proliferator-activated receptors (PPARs) are transcription factors belonging to the family of nuclear receptors that regulate glucose homeostasis, inflammation, and lipid metabolism. Three proteins, encoded by distinct genes, have been identified: PPAR-α, PPAR-β/δ, and PPAR-γ, which control gene expression by binding to PPREs in the promoters [239] . The activation of PPARs is a tightly regulated process implicated in the control of lipid homeostasis, which involves the biogenesis of LDs and protein expression involved in lipid uptake, including PRRs and structural protein PLIN2, and enzymes implicated in neutral lipid synthesis (triacylglycerol and cholesterol) [240] . PPARs have been demonstrated to increase in foam macrophages [241] . In this sense, it was revealed that MT-III induced the upregulation of the transcription factors PPAR-γ and PPAR-β/δ, in addition to the translocation of these factors to the nucleus of mouse peritoneal macrophages. The pharmacological blockage of the PPAR-β/δ transcription factor abolished the increase in PLIN2 and CD36 protein expression induced by MT-III. Moreover, the PPAR-γ blockage caused a reduction in LD formation and abolished CD36 receptor protein expression induced by MT-III. Since an increased expression of CD36 and PLIN2 is related to macrophage differentiation into foam cells [242, 243] , these findings suggest that MT-III induces foam cell formation by this route. In addition, MT-III caused an increase in the levels of triacylglycerol and cholesterol due to the uptake of free fatty acids. These effects were mediated by DGAT and ACAT enzymes, which are involved in the synthesis of triacylglycerol and cholesterol, respectively [244] . In agreement with this study, a significant increase in triacylglycerol and cholesterol levels was observed in human monocytes under MT-III stimulation [222] . This effect was dependent on fatty acid reacylation. Moreover, the fatty acid composition of triacylglycerol and cholesterol induced by MT-III was compatible with fatty acids released by the enzymatic action of this svPLA 2 on cell membranes. According to the above information, the mechanisms triggered by MT-III, in both mice peritoneal macrophages and human monocytes, align with macrophages differentiation into foamy cells, a cell type characteristic of inflammatory metabolic diseases, such as atherosclerosis [245] . Similarly, MT-III could stimulate LD formation in VSCMs. This lipid accumulation was likewise mediated by the activation of transcription factors PPAR-γ and PPAR-β/δ and DGAT and ACAT enzymes. Moreover, it is noteworthy that VSCMs under stimulation of MT-III exhibited an increase in the protein levels of PRRs, SRA-1 (scavenger receptor type 1), and LOX-1 (lectin-like oxidized low-density lipoprotein receptor-1). Interestingly, the blockage of these receptors did not alter the formation of LDs induced by MT-III, but the upregulation of LOX-1 was associated with an increased uptake of acetylated-low density lipoprotein (acLDL) in VSMCs stimulated by this svPLA 2 . This higher uptake of acLDL by VSMCs identifies new pathways involved in the accumulation of lipids triggered by a sPLA 2 that is not directly linked to the reacylation of free fatty acids. In addition, lipid accumulation induced by MT-III in VSCMs was related to the expression of ATP-binding cassette transporters ABCA1 and ABCG1, responsible for the efflux of cholesterol of macrophage-derived foam cells [242] . Although the signaling pathway by which MT-III induces an increased expression of the factors implicated in lipid homeostasis has not been fully elucidated, these studies have broadened the knowledge about the actions of svPLA 2 s on the formation of LDs and the synthesis of lipid mediators and provided new insights into the actions of group IIA sPLA 2 s in diseases related to lipid imbalance. The pathways and factors involved in lipid accumulation in an innate immune cell (macrophage) upon stimulus by svPLA 2 s are summarized in Figure 4 .

Another aspect related to the metabolism of free fatty acids is the biosynthesis of lipid mediators [246] [247] [248] . On the one hand, it is known that the synthesis of eicosanoids is closely related to the triggering of the inflammatory process induced by svPLA 2 s, regardless of the catalytic activity on the cell membranes [13] . In this sense, the immunofluorescence approach has demonstrated that LDs stimulated by svPLA 2 s synthesize PGE 2 [167, 249] . On the other hand, some eicosanoids are implicated in the resolution of inflammatory processes, such as PGJ 2 . This mediator was co-located in LDs in macrophage peritoneal mice stimulated by MT-II [161] , indicating, for the first time, that the LDs not only are related to the production of inflammatory mediators but also might play a role in regulating this process.

Adipose tissue is the principal organ responsible for balancing energy metabolism in the mammalian body. An imbalance in adipose tissue functions is linked to the triggering of the inflammatory process observed in metabolic diseases, including obesity [250, 251] .

Recently, it has been demonstrated that MT-III activated proinflammatory mechanisms in 3T3-L1 preadipocytes, including the biosynthesis of PGE 2 and PGI 2 , lipid mediators impli-cated in preadipocytes differentiation into mature adipocytes, and IL-6 and MCP-1 [169] . In these cells, PGE 2 production induced by MT-III was dependent on cPLA 2 activation, the upregulation of COX-2 and mPGES-1, and the engagement of the PGE 2 EP4 receptor. In addition, the release of IL-6 and MCP-1 was dependent on EP4 or EP3 activation, respectively. These data indicate that the production of PGE 2 is critical for the activation of proinflammatory pathways associated with cytokine production in preadipocytes stimulated by this svPLA 2 . Furthermore, MT-III upregulated the gene expression of the adipokines leptin and adiponectin in preadipocytes [169] . These mediators have been described as regulating appetite and satiety, glucose and lipid metabolism, inflammation, and immune functions [252] [253] [254] [255] . Although the mechanisms related to the release of adipokines and the ability of MT-III to induce lipid accumulation in adipocytes have not yet been investigated, these data offer new directions for investigating the actions triggered by svPLA 2 s and mammalian GIIA sPLA 2 s.

inflammatory metabolic diseases, such as atherosclerosis [245] . Similarly, MT-III could stimulate LD formation in VSCMs. This lipid accumulation was likewise mediated by the activation of transcription factors PPAR-γ and PPAR-β/δ and DGAT and ACAT enzymes. Moreover, it is noteworthy that VSCMs under stimulation of MT-III exhibited an increase in the protein levels of PRRs, SRA-1 (scavenger receptor type 1), and LOX-1 (lectin-like oxidized low-density lipoprotein receptor-1). Interestingly, the blockage of these receptors did not alter the formation of LDs induced by MT-III, but the upregulation of LOX-1 was associated with an increased uptake of acetylated-low density lipoprotein (acLDL) in VSMCs stimulated by this svPLA2. This higher uptake of acLDL by VSMCs identifies new pathways involved in the accumulation of lipids triggered by a sPLA2 that is not directly linked to the reacylation of free fatty acids. In addition, lipid accumulation induced by MT-III in VSCMs was related to the expression of ATP-binding cassette transporters ABCA1 and ABCG1, responsible for the efflux of cholesterol of macrophage-derived foam cells [242] . Although the signaling pathway by which MT-III induces an increased expression of the factors implicated in lipid homeostasis has not been fully elucidated, these studies have broadened the knowledge about the actions of svPLA2s on the formation of LDs and the synthesis of lipid mediators and provided new insights into the actions of group IIA sPLA2s in diseases related to lipid imbalance. The pathways and factors involved in lipid accumulation in an innate immune cell (macrophage) upon stimulus by svPLA2s are summarized in Figure 4 . . Schematic representation of the mechanisms and factors involved in lipid accumulation induced by svPLA2s, in macrophages. svPLA2 acts on membrane phospholipids generating free fatty acids, which are ligands of and may activate the TLR2, CD36, and cytoplasmic transcription receptors and factors PPARs. svPLA2 induces the activation of transcription factors PPAR-γ and PPAR-δ/β and increases protein expression of PPARs and CD36. PPAR-γ, PPAR-β/δ, TLR2/MyD88, and CD36 receptors, as well as DGAT and ACAT enzymes are involved in the lipid droplets formation stimulated by MT-III. PPAR-β/δ, but not PPAR-γ, is implicated in upregulation of PLIN2 protein expression, induced by MT-III. Moreover, TLR2 and the Myd88 adaptor molecules participate in the recruitment of the PLIN2 protein via cytoskeleton activation Figure 4 . Schematic representation of the mechanisms and factors involved in lipid accumulation induced by svPLA 2 s, in macrophages. svPLA 2 acts on membrane phospholipids generating free fatty acids, which are ligands of and may activate the TLR2, CD36, and cytoplasmic transcription receptors and factors PPARs. svPLA 2 induces the activation of transcription factors PPAR-γ and PPAR-δ/β and increases protein expression of PPARs and CD36. PPAR-γ, PPAR-β/δ, TLR2/MyD88, and CD36 receptors, as well as DGAT and ACAT enzymes are involved in the lipid droplets formation stimulated by MT-III. PPAR-β/δ, but not PPAR-γ, is implicated in upregulation of PLIN2 protein expression, induced by MT-III. Moreover, TLR2 and the Myd88 adaptor molecules participate in the recruitment of the PLIN2 protein via cytoskeleton activation stimulated by MT-III. In addition, LD formation induced by svPLA 2 is dependent on activation of PKC, PI3K, p38MAP, ERK, cPLA 2 , and iPLA 2 signaling pathways.

The existing literature demonstrates that the svPLA 2 s trigger a cascade of inflammatory events including edema formation, leukocyte recruitment into tissues, release of a complex network of inflammatory mediators, and increased oxidative stress in experimental animal models that mimic the inflammatory responses elicited by viperid snake venoms, especially those from the Bothrops genus, in the victims. The catalytic activity of the svPLA 2 s is not strictly required by these proteins for the triggering of all the inflammatory responses, since the catalytically inactive Lys49 PLA 2 variants can display inflammatory events that are qualitatively similar to those of Asp49 PLA 2 s. In addition to cell migration, the svPLA 2 s can activate distinct functions of immunocompetent cells that include phagocytosis, the respiratory burst, NET formation, production of cytokines, chemokines and multiple reactive cleavage products such as lysophospholipids, polyunsaturated fatty acids and eicosanoids, as well as formation of LDs. The highly complex network of mediators, particularly lipid mediators, modulates a variety of inflammatory events triggered by this class of snake venom toxins. The effects triggered by svPLA 2 s in inflammatory cells that lead to generation of lipid mediators has been associated with the activation of distinct signaling pathways of inflammatory kinase proteins by mechanisms dependent and independent of NF-kB. Moreover, the inflammatory response elicited by svPLA 2 s in leukocytes also involves upregulation of PRRs of innate immune response, the crosstalk between the svPLA 2 and intracellular PLA 2 s, and upregulation of factors implicated in lipid homeostasis. Although much has been learned regarding the inflammatory actions of svPLA 2 s, many knowledge gaps still exist and need to be addressed. There is still considerable work to be done before we fully understand the complex interactions that occur among svPLA 2 s and immunocompetent cells and tissues that lead to inflammation. The cell acceptors and/or receptors involved in the actions of svPLA 2 s in these cells and the signaling pathways elicited and how they interact with each other remain to be clarified. In addition, the actual types and subtypes of receptors activated by the principal mediators produced by svPLA 2 s and the mechanisms involved in coupling between the svPLA 2 s and endogenous PLA 2 s have yet to be investigated. Recently, the stimulatory activity of a svPLA 2 on adipose tissue cells leading to increased biosynthesis of PGE 2 and other inflammatory mediators including adipokines was demonstrated. This information offers new directions for investigating the actions triggered by svPLA 2 s and mammalian GIIA sPLA 2 and gives insights into the potential role of the adipocytes as target cells for viperid snake venoms. Finally, a deeper and comprehensive understanding of the mechanisms underlying the inflammatory actions of svPLA 2 s will give new insights into (i) the actions of group IIA sPLA 2 s in diseases related to lipid imbalance and inflammation and (ii) a better understanding of the pathophysiology of Bothrops envenomation. Within this frame, the acquired knowledge might pave the way for the development of novel therapeutic approaches aimed at counteracting the prominent inflammation caused by Bothrops snakebite envenoming. 

The authors declare no conflict of interest.

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PGAP6, a GPI-specific phospholipase A2, has narrow substrate specificity against GPI-anchored proteins

Phospholipases: An Overview

Secretory phospholipase A2 enzymes as pharmacological targets for treatment of disease

Secreted phospholipases A2 of snake venoms: Effects on the peripheral neuromuscular system with comments on the role of phospholipases A2 in disorders of the CNS and their uses in industry

Activation of human inflammatory cells by secreted phospholipases A2

What can venom phospholipases A2 tell us about the functional diversity of mammalian secreted phospholipases A2?

Phospholipase A2 enzymes

Excitement ahead: Structure, function and mechanism of snake venom phospholipase A2 enzymes

Identification and properties of very high affinity brain membranebinding sites for a neurotoxic phospholipase from the taipan venom

Identification and purification of a very high affinity binding protein for toxic phospholipases A2 in skeletal muscle

Presence of the M-type sPLA 2 receptor on neutrophils and its role in elastase release and adhesion

Activation of Cytokine Production by Secreted Phospholipase A 2 in Human Lung Macrophages Expressing the M-Type Receptor

Phospholipase A2 receptor: A regulator of biological functions of secretory phospholipase A2

The structure and function of vertebrate mannose lectin-like proteins

Primary structure of the mannose receptor contains multiple motifs resembling carbohydrate-recognition domains

Macrophage Activation Markers, Soluble CD163 and Mannose Receptor, in Liver Fibrosis

Molecular immunobiology of macrophages: Recent progress

Macrophage Biology and Pathobiology in the Evolution of Immune Responses: A Functional Analysis

Secretory Phospholipase A2 Activates the Cascade of Mitogen-activated Protein Kinases and Cytosolic Phospholipase A2 in the Human Astrocytoma Cell Line 1321N1

Activation of MAP kinase cascade induced by human pancreatic phospholipase A2 in a human pancreatic cancer cell line

Evidence that porcine pancreatic phospholipase A2 via its high affinity receptor stimulates extracellular matrix invasion by normal and cancer cells

Metabolism of Lipid Mediators in Human Eosinophils

Amino Acid Composition and NH2-Terminal Amino Acid Sequence of Human Phospholipase A2 Purified from Rheumatoid Synovial Fluid1

Mammalian Secreted Phospholipases A2 and Their Pathophysiolo-gical Significance in Inflammatory Diseases

Point of care testing of phospholipase A2 group IIA for serological diagnosis of rheumatoid arthritis

A Novel Hypothetical Approach to Explain the Mechanisms of Pathogenicity of Rheumatic Arthritis

Pancreatic phospholipase A2 activity in acute pancreatitis: A prognostic marker for early identification of patients at risk

Effect of phospholipase A2 silencing on acute experimental pancreatitis

Serum Phospholipase A 2 in Human Acute Pancreatitis

Role of secretory phospholipases A2 in the pathobiology of disease

High sPLA2-IIA level is associated with eicosanoid metabolism in patients with bacterial sepsis syndrome

Phospholipase A2 in serum and colonic mucosa in ulcerative colitis

Gene Expression of Group Ii Phospholipase A2 in Intestine in Crohn's Disease

A potent and selective inhibitor of group IIa secretory phospholipase A2 protects rats from TNBS-induced colitis

Characterization of phospholipase A2 from human nasal lavage

Bronchoalveolar lavage fluid phospholipase A2 activities are increased in human adult respiratory distress syndrome

Secretory Phospholipase A2 Enzymes in Acute Lung Injury

The role of mast cell-derived secreted phospholipases A2 in respiratory allergy

Elevated Type II Secretory Phospholipase A2 Increases the Risk of Early Atherosclerosis in Patients with Newly Diagnosed Metabolic Syndrome

Secretory phospholipase A2 of group IIA: Is it an offensive or a defensive player during atherosclerosis and other inflammatory diseases?

Secreted phospholipase A2 activity in experimental autoimmune encephalomyelitis and multiple sclerosis

Group IIA phospholipase A2 as a prognostic marker in prostate cancer: Relevance to clinicopathological variables and disease-specific mortality

Secretory phospholipase A2-IIa is involved in prostate cancer progression and may potentially serve as a biomarker for prostate cancer

Group IIa secretory phospholipase A2 (sPLA2IIa) and progression in patients with lung cancer

A Concise Update on the Relevance of Secretory Phospholipase A2 Group IIA and its Inhibitors with Cancer

Interleukin-1β, tumor necrosis factor and forskolin stimulate the synthesis and secretion of group II phospholipase A2 in rat mesangial cells

The secretory phospholipase A2 group IIA: A missing link between inflammation, activated reninangiotensin system, and atherogenesis? Vasc. Health Risk Manag

Multiple phospholipase A2 enzymes participate in the inflammatory process in osteoarthritic cartilage

Potentiation of Tumor Necrosis Factor α-induced Secreted Phospholipase A2 (sPLA2)-IIA Expression in Mesangial Cells by an Autocrine Loop Involving sPLA2 and Peroxisome Proliferator-activated Receptor α Activation

Secreted phospholipase A2 of Clonorchis sinensis activates hepatic stellate cells through a pathway involving JNK signalling

sPLA 2 -IIA Overexpression in Mice Epidermis Depletes Hair Follicle Stem Cells and Induces Differentiation Mediated Through Enhanced JNK/c-Jun Activation

Group IIA secretory phospholipase A2 stimulates inducible nitric oxide synthase expression via ERK and NF-κB in macrophages

Secreted phospholipases A2 induce the expression of chemokines in microvascular endothelium

Origin and physiological roles of inflammation

A calculated response: Control of inflammation by the innate immune system

Neutrophils: Between Host Defence, Immune Modulation, and Tissue Injury

Chemokines and chemokine receptors: An overview

Role of Histamine in Modulating the Immune Response and Inflammation

Adhesion molecules and their role in vascular disease

Principles of Leukocyte Migration Strategies

Phagocytosis: A Fundamental Process in Immunity

Phagocytosis: An Immunobiologic Process

The carbohydrate switch between pathogenic and immunosuppressive antigen-specific antibodies

TLR-mediated innate immune recognition

Toll-like receptors in the induction of the innate immune response

NOD-Like Receptors: Versatile Cytosolic Sentinels

Innate immune receptors for cross-presentation: The expanding role of NLRs

Localisation and trafficking of Toll-like receptors: An important mode of regulation

The role of pattern-recognition receptors in innate immunity: Update on toll-like receptors

Inflammasomes: Mechanism of assembly, regulation and signalling

Regulation of inflammasome signaling

Inflammasomes in health and disease

Inflammasome activation and assembly at a glance

Inhibition of Nuclear Translocation of Transcription Factor NF-κB by a Synthetic Peptide Containing a Cell Membrane-permeable Motif and Nuclear Localization Sequence

The nuclear factor NF-kappaB pathway in inflammation

Signaling pathways in phagocytosis

Regulation of Highly Cytokinergic IgE-Induced Mast Cell Adhesion by Src, Syk, Tec, and Protein Kinase C Family Kinases

The role of tyrosine phosphorylation of protein kinase C delta in infection and inflammation

The PI3K Pathway in Human Disease

Purification of the human alveolar macrophage mannose receptor

Molecular characterization of the human macrophage mannose receptor: Demonstration of multiple carbohydrate recognition-like domains and phagocytosis of yeasts in Cos-1 cells

Modular components of phagocytosis

Mannose-Containing Molecular Patterns Are Strong Inducers of Cyclooxygenase-2 Expression and Prostaglandin E 2 Production in Human Macrophages

Interleukin-4-induced macrophage fusion is prevented by inhibitors of mannose receptor activity

Inhibitors of p38 Mitogen-Activated Protein Kinase

Cellular Regulation of the Inflammatory Response

Proresolving Lipid Mediators and Mechanisms in the Resolution of Acute Inflammation

Resolution of inflammation: The beginning programs the end

Is Resolution the End of Inflammation?

A guiding map for inflammation

Accelerated Evolution and Molecular Surface of Venom Phospholipase A2 Enzymes

The primary structure of ammodytin L, a myotoxic phospholipase A2 homologue from Vipera ammodytes venom

Solution structure of porcine pancreatic phospholipase A2

The effect of myotoxins isolated from Bothrops snake venoms on multilamellar liposomes: Relationship to phospholipase A2, anticoagulant and myotoxic activities

Phospholipases A2 from viperidae snake venoms: How do they induce skeletal muscle damage?

Inflammatory events induced by Lys-49 and Asp-49 phospholipases A2 isolated from Bothrops asper snake venom: Role of catalytic activity

Inflammatory effects of snake venom myotoxic phospholipases A2

Inflammatory oedema induced by the Lys-49 phospholipase A2 homologue piratoxin-I in the rat and rabbit. Effect of polyanions and p-bromophenacyl bromide

Pharmacological modulation of edema induced by Lys-49 and Asp-49 myotoxic phospholipases A2 isolated from the venom of the snake Bothrops asper (Terciopelo)

Kinetic and Pharmacological Characterization of Phospholipases A2 from Bothrops neuwiedii Venom

Mast cell degranulation induced by two phospholipase A2 homologues: Dissociation between enzymatic and biological activities

Isolation, characterization and biological activity of acidic phospholipase A2 isoforms from Bothrops jararacussu snake venom

Purification, sequencing and structural analysis of two acidic phospholipases A2 from the venom of Bothrops insularis (jararaca ilhoa)

Leucocyte recruitment induced by type II phospholipases A2 into the rat pleural cavity

Biochemical and biological properties of phospholipases A2 from Bothrops atrox snake venom

Mast cells

Mast cells-Key effector cells in immune responses

Hyperalgesia induced by Asp49 and Lys49 phospholipases A2 from Bothrops asper snake venom: Pharmacological mediation and molecular determinants

Human neutrophil migration in vitro induced by secretory phospholipases A2: A role for cell surface glycosaminoglycans

Signalling pathways regulating human neutrophil migration induced by secretory phospholipases A2

Signaling pathways involved in zymosan phagocytosis induced by two secreted phospholipases A2 isolated from Bothrops asper snake venom in macrophages

Insights of local tissue damage and regeneration induced by BnSP-7, a myotoxin isolated from Bothrops (neuwiedi) pauloensis snake venom

Immune cells and mediators involved in the inflammatory responses induced by a P-I metalloprotease and a phospholipase A2 from Bothrops atrox venom

Cytotoxic and inflammatory potential of a phospholipase A2 from Bothrops jararaca snake venom

Cytokines in the rheumatic diseases

Exploring the complex role of chemokines and chemoattractants in vivo on leukocyte dynamics

Neutrophil migration in infection and wound repair: Going forward in reverse

Pharmacological, and Structural Characterization of New Basic Bbil-TX from Bothriopsis bilineata Snake Venom

Purification and Biochemical Characterization of Three Myotoxins from Bothrops mattogrossensis Snake Venom with Toxicity against Leishmania and Tumor Cells

Inflammasome Activation Induced by a Snake Venom Lys49-Phospholipase A2 Homologue

Inflammatory effect of Bothropstoxin-I from Bothrops jararacussu venom mediated by NLRP3 inflammasome involves ATP and P2X7 receptor

Action of two phospholipases A2 purified from Bothrops alternatus snake venom on macrophages

Biochemical Characterization, Action on Macrophages, and Superoxide Anion Production of Four Basic Phospholipases A 2 from Panamanian Bothrops asper Snake Venom

Activation of cellular functions in macrophages by venom secretory Asp-49 and Lys-49 phospholipases A2

Activation of J77A.1 macrophages by three phospholipases A2 isolated from Bothrops atrox snake venom

Beneficial suicide: Why neutrophils die to make NETs

Neutrophils and NETs in modulating acute and chronic inflammation

Human neutrophils functionality under effect of an Asp49 phospholipase A2 isolated from Bothrops atrox venom

Different Evolution of Phospholipase A 2 Neurotoxins (Beta-Neurotoxins) from Elapidae and Viperidae Snakes

Presynaptic enzymatic neurotoxins

Contribution of crotoxin for the inhibitory effect of Crotalus durissus terrificus snake venom on macrophage function

Inhibitory effect of phospholipase A2 isolated from Crotalus durissus terrificus venom on macrophage function

Crotoxin Isolated from Crotalus durissus terrificus Venom Modulates the Functional Activity of Dendritic Cells via Formyl Peptide Receptors

A snake venom group IIA PLA2 with immunomodulatory activity induces formation of lipid droplets containing 15-d-PGJ2 in macrophages

A catalyticallyinactive snake venom Lys49 phospholipase A2 homolog induces expression of cyclooxygenase-2 and production of prostaglandins through selected signaling pathways in macrophages

Effects of Bothrops asper snake venom on the expression of cyclooxygenases and production of prostaglandins by peritoneal leukocytes in vivo, and by isolated neutrophils and macrophages in vitro

An asp49 phospholipase A2 from snake venom induces cyclooxygenase-2 expression and prostaglandin E2 production via activation of NF-κ B, p38MAPK, and PKC in macrophages

A phospholipase A2 from Bothrops asper snake venom activates neutrophils in culture: Expression of cyclooxygenase-2 and PGE2 biosynthesis

12-HETE is a regulator of PGE2 production via COX-2 expression induced by a snake venom group IIA phospholipase A2 in isolated peritoneal macrophages

A Lys49 phospholipase A2, isolated from Bothrops asper snake venom, induces lipid droplet formation in macrophages which depends on distinct signaling pathways and the C-terminal region

A secreted phospholipase A2 induces formation of smooth muscle foam cells which transdifferentiate to macrophage-like state

A Representative GIIA Phospholipase A2 Activates Preadipocytes to Produce Inflammatory Mediators Implicated in Obesity Development

A snake venom-secreted phospholipase A2 induces foam cell formation depending on the activation of factors involved in lipid homeostasis

Regulatory functions of phospholipase A2

cDNA Cloning and Mutagenesis Study of Leukotriene B4 12-Hydroxydehydrogenase

In vitro and in vivo pharmacological characterization of SB 201993, an eicosanoid-like LTB4receptor antagonist with anti-inflammatory activity

Aspirin-Triggered 15-Epi-Lipoxin A4 and Stable Analogs of Lipoxin A4 are Potent Inhibitors of Acute Inflammation

Transfection of an Active Cytochrome P450 Arachidonic Acid Epoxygenase Indicates That 14,15-Epoxyeicosatrienoic Acid Functions as an Intracellular Second Messenger in Response to Epidermal Growth Factor

Leukotrienes and Lipoxins: Structures, Biosynthesis, and Biological Effects

Cyclooxygenases and prostaglandins: Shaping up the immune response

Expression of mRNA for cyclooxygenase-1 and cyclooxygenase-2 in human tissues

Isolation and characterization of the complementary DNA for sheep seminal vesicle prostaglandin endoperoxide synthase (cyclooxygenase)

Human platelet/erythroleukemia cell prostaglandin G/H synthase: cDNA cloning, expression, and gene chromosomal assignment

Cyclooxygenase-1 (COX-1) and COX-1 inhibitors in cancer: A review of oncology and medicinal chemistry literature

Regulation of the cellular expression of secretory and cytosolic phospholipases A2, and cyclooxygenase-2 by peptide growth factors

Prostaglandin E2 as a Regulator of Immunity to Pathogens

Cyclooxygenase-2 (COX-2) in Inflammatory and Degenerative Brain Diseases

Cyclooxygenase in normal human tissues-Is COX-1 really a constitutive isoform, and COX-2 an inducible isoform?

Secretory phospholipases A2 isolated from Bothrops asper and from Crotalus durissus terrificus snake venoms induce distinct mechanisms for biosynthesis of prostaglandins E2 and D2 and expression of cyclooxygenases

Physiological and pathophysiological roles of eicosanoids in the microcirculation

Diverse effects of prostaglandin e2on vascular contractility

Pharmacological activities of a toxic phospholipase a isolated from the venom of the snake Bothrops asper

Bothrops jararaca and Crotalus durissus terrificus venoms elicit distinct responses regarding to production of prostaglandins E2 and D2, and expression of cyclooxygenases

The role of enzymatic activity in inhibition of the extrinsic tenase complex by phospholipase A2 isoenzymes from Naja nigricollis venom

Selective inhibitors of cytosolic or secretory phospholipase A2 block TNF-induced activation of transcription factor nuclear factor-kappa B and expression of ICAM-1

Functional Coupling between Secretory and Cytosolic Phospholipase A2 Modulates Tumor Necrosis Factor-α-and Interleukin-1β-induced NF-κB Activation

Functional coupling between secretory phospholipase A2 and cyclooxygenase-2 and its regulation by cytosolic group IV phospholipase A2

Phospholipase A2 superfamily in cancer

Segregated coupling of phospholipases A2, cyclooxygenases, and terminal prostanoid synthases in different phases of prostanoid biosynthesis in rat peritoneal macrophages

Cytosolic Phospholipase A2 Is Required for Cytokine-induced Expression of Type IIA Secretory Phospholipase A2 That Mediates Optimal Cyclooxygenase-2-dependent Delayed Prostaglandin E2 Generation in Rat 3Y1 Fibroblasts

The Functions of Five Distinct Mammalian Phospholipase A2s in Regulating Arachidonic Acid Release

Perinuclear localization of cytosolic phospholipase A 2 α is important but not obligatory for coupling with cyclooxygenases

Role of Cytosolic Phospholipase A 2 in Prostaglandin E 2 Production by Lung Fibroblasts

TPL-2 kinase regulates the proteolysis of the NF-κB-inhibitory protein NF-κB1 p105

Regulation of MAP kinase by calciumsensing receptor in bovine parathyroid and CaR-transfected HEK293 cells

Mechanism of ATP-Induced [Ca 2+ ] i Mobilization in Rat Basilar Smooth Muscle Cells

Critical role of TLR2 and MyD88 for functional response of macrophages to a group IIA-secreted phospholipase A2from snake venom

Pérez-Torres, I. Participation of arachidonic acid metabolism in the aortic aneurysm formation in patients with Marfan syndrome

Signaling Mechanism Underlying COX-2 Induction by Lysophosphatidylcholine

Arachidonic acid, an omega-6 fatty acid, induces cytoplasmic phospholipase A 2 in prostate carcinoma cells

Group V Phospholipase A 2 -Derived Lysophosphatidylcholine Mediates Cyclooxygenase-2 Induction in Lipopolysaccharide-Stimulated Macrophages

Lipid droplet biogenesis induced by stress involves triacylglycerol synthesis that depends on Group VIA phospholipase A2

Simultaneous activation of p38 and JNK by arachidonic acid stimulates the cytosolic phospholipase A2-dependent synthesis of lipid droplets in human monocytes

Lipid droplets induced by secreted phospholipase A2 and unsaturated fatty acids protect breast cancer cells from nutrient and lipotoxic stress

Lipid droplets as signaling platforms linking metabolic and cellular functions

Lipid Droplets in Health and Disease. Lipids Health Dis

Expanding roles for lipid droplets

Mammalian lipid droplets are innate immune hubs integrating cell metabolism and host defense

Lipid-Droplet Formation Drives Pathogenic Group 2 Innate Lymphoid Cells in Airway Inflammation

Lipid-droplet-accumulating microglia represent a dysfunctional and proinflammatory state in the aging brain

High plasma phospholipase A 2 activity, inflammation markers, and LDL alterations in obesity with or without type 2 diabetes

Cholesterol, inflammation and innate immunity

Atherosclerosis: The interplay between lipids and immune cells

A lipidomic perspective of the action of group iia secreted phospholipase a2 on human monocytes: Lipid droplet biogenesis and activation of cytosolic phospholipase a2α

The Cytoskeleton as Regulator of Cell Signaling Pathways

A group IIA-secreted phospholipase A2 from snake venom induces lipid body formation in macrophages: The roles of intracellular phospholipases A2 and distinct signaling pathways

PKC-ALDH2 pathway plays a novel role in adipocyte differentiation

Signaling pathway of magnolol-stimulated lipolysis in sterol ester-loaded 3T3-L1 preadipocyes

Dugail, I. Cholesterol-induced caveolin targeting to lipid droplets in adipocytes: A role for caveolar endocytosis

Lipid droplet and milk lipid globule membrane associated placental protein 17b (PP17b) is involved in apoptotic and differentiation processes of human epithelial cervical carcinoma cells

Oleic acid-induced perilipin 5 expression and lipid droplets formation are regulated by the PI3K/PPARα pathway in HepG2 cells

Apolipoprotein CIII regulates lipoprotein-associated phospholipase A2 expression via the MAPK and NFκB pathways

9t18:1 and 11t18:1 activate the MAPK pathway to regulate the expression of PLA2 and cause inflammation in HUVECs

PLD1 and ERK2 regulate cytosolic lipid droplet formation

The assembly of lipid droplets and its relation to cellular insulin sensitivity

Role of p38 MAPK in atherosclerosis and aortic valve sclerosis

The walking dead: Macrophage inflammation and death in atherosclerosis

Phospholipase A2 isoforms: A perspective

Role of Ca2+-independent phospholipase A2 in cell growth and signaling

Cytosolic phospholipase A 2 and lysophospholipid acyltransferases

Peroxisome proliferator-activated receptors and their ligands: Nutritional and clinical implications-A review

Chlamydia pneumoniae induces macrophage-derived foam cell formation via PPAR α and PPAR γ-dependent pathways

Mechanisms of foam cell formation in atherosclerosis

Perilipin 2 (PLIN2)-deficiency does not increase cholesterol-induced toxicity in macrophages

Regulation of Triglyceride Metabolism. I. Eukaryotic neutral lipid synthesis

Foam cells in atherosclerosis

Lipid droplets: Platforms with multiple functions in cancer hallmarks

Lipid droplets fuel SARS-CoV-2 replication and production of inflammatory mediators

A twist of FATe: Lipid droplets and inflammatory lipid mediators

Crotalus durissus ruruima Snake Venom and a Phospholipase A2 Isolated from This Venom Elicit Macrophages to Form Lipid Droplets and Synthesize Inflammatory Lipid Mediators

Adipose tissue: A regulator of inflammation

The role of adipose tissue in cardiovascular health and disease

The weight of leptin in immunity

Adiponectin induces TNF-α and IL-6 in macrophages and promotes tolerance to itself and other pro-inflammatory stimuli

Adiponectin inhibits Toll-like receptor family-induced signaling

There and back again: Leptin actions in white adipose tissue