key: cord-0012466-vku6fecr
authors: Chellan, Bijoy; Rojas, Elizabeth; Zhang, Chunling; Hofmann Bowman, Marion A.
title: Enzyme-modified non-oxidized LDL (ELDL) induces human coronary artery smooth muscle cell transformation to a migratory and osteoblast-like phenotype
date: 2018-08-10
journal: Sci Rep
DOI: 10.1038/s41598-018-30073-w
sha: bd135416ced089d402145d841fcda38d8b7d35f5
doc_id: 12466
cord_uid: vku6fecr

Enzyme modified non-oxidative LDL (ELDL) is effectively taken up by vascular smooth muscle cells (SMC) and mediates transition into foam cells and produces phenotypic changes in SMC function. Our data show that incubation of human coronary artery SMC (HCASMC) with low concentration of ELDL (10 μg/ml) results in significantly enhanced foam cell formation compared to oxidized LDL (200 μg/ml; p < 0.01) or native LDL (200 μg/ml; p < 0.01). Bioinformatic network analysis identified activation of p38 MAPK, NFkB, ERK as top canonical pathways relevant for biological processes linked to cell migration and osteoblastic differentiation in ELDL-treated cells. Functional studies confirmed increased migration of HCASMC upon stimulation with ELDL (10 μg/ml) or Angiopoietin like protein 4, (ANGPTL4, 5 μg/ml), and gain in osteoblastic gene profile with significant increase in mRNA levels for DMP-1, ALPL, RUNX2, OPN/SPP1, osterix/SP7, BMP and reduction in mRNA for MGP and ENPP1. Enhanced calcification of HCASMC by ELDL was demonstrated by Alizarin Red staining. In summary, ELDL is highly potent in inducing foam cells in HCASMC and mediates a phenotypic switch with enhanced migration and osteoblastic gene profile. These results point to the potential of ELDL to induce migratory and osteoblastic effects in human smooth muscle cells with potential implications for migration and calcification of SMCs in human atherosclerosis.

ELDL was previously shown to be more potent than OxLDL in inducing foam cells in cultured macrophages 9 ; and more recently, our laboratory demonstrated its ability to foam murine aortic SMCs at lower concentrations compared to OxLDL or native LDL 7 . However, such comparative studies in human SMC are lacking. We cultured human coronary artery smooth muscle cells (HCASMC) for 24 h with ELDL, OxLDL or native LDL in indicated concentration of lipoprotein (based on protein content) and the cellular lipid content was visualized by staining with Oil Red O after 24 hours as shown in Fig. 1a . As expected, ELDL was very effectively taken up by HCASMCs and induced foam cell formation at low concentration of 10 µg/ml. ELDL at 10 and 25 μg/mL lipoprotein-protein induced dose dependent accumulation of lipid, whereas cell death was observed at 100 μg/mL of ELDL, probably due to high cholesterol toxicity. However, substantially higher concentrations of OxLDL (200 μg/mL) were required for foam cell formation. The small amount of intracellular lipid accumulation induced by OxLDL at 200 μg/mL was further associated with significant cell death as evidenced by trypan blue staining (≈75%, data not shown). Unmodified native LDL induced foam cells formation at 100 and 200 μg/mL and no cytotoxicity was observed (data not shown). Taken together, total cell cholesterol content was significantly increased in HCASMC upon treatment with ELDL compared to OxLDL and native LDL when compared to same amount of lipoprotein based on protein measurement of LDL as shown upon quantification in Fig. 1b . Moreover, similar results were obtained upon quantification of lipoproteins based on cholesterol content after taking into account that ELDL has slightly more cholesterol per 10 µg protein concentration ( Supplementary Figs 1 and 2) . ELDL uptake and foaming of HCASMCs induced gene expression of some adipocyte markers (FABp4, perilipin), although many others genes for adipocytes or smooth muscle cell were similarly expressed in ELDL and BSA control cells (Supplementary Fig. 3 ).

We next studied the effect of cholesterol treatment on gene expression in cultured HCASMC. HCASMC were stimulated with 50 μg/ mL cholesterol (either as native LDL, oxidized LDL, or ELDL) and compared to BSA incubated control HCASMC. Whole genome gene expression was profiled using microarray chips (Illumina Bead Chip HT-12v4 array containing more than 47.000 probes). All samples passed basic quality control and the principle component analysis (PCA) showed a similar gene expression pattern for each of the three biological replicates of the four major treatment groups (Fig. 2a) . Differentially expressed genes (DEGs) for each comparison were created for hierarchical clustering visualization. We analyzed data with cutoff criteria for gene expression ≥1.5 fold change and ≥2 fold change with a false discovery rate of <0.05. For the 1.5 fold cutoff criteria, 27 genes in cells treated with native LDL, 1393 genes for OxLDL, and 103 genes for ELDL treated cells were differentially expressed (Fig. 2b) . The number of genes overlapping the four groups of differentially expressed genes is shown in Fig. 2c . Interestingly, of the 1393 genes differentially expressed in OxLDL treated cells, there were overlaps with only 74 genes in ELDL treated cells. Moreover, 1310 genes were only in the OxLDL list, and 25 genes only in the ELDL list. For example, the common subset of genes that belong to the intersect of DEGs detected in the LDL vs control (BSA) intersecting with OxLDL vs control BSA and ELDL vs control BSA is corresponding to only one gene. The criteria that was used to define the statistical significance of the detected DEG was that the FDR corrected p-value must be ≤0.05 and the absolute value of the fold change must be ≥1.5. From these only 3 belong to the intersection between OxLDL vs control and ELDL vs control, but these 3 don't intersect with LDL vs. control as shown in Fig. 2c . Taken together, this suggests that gene expression is distinctly different between HCASMC stimulated with oxidized LDL compared to ELDL or native LDL. Hierarchical clustering for each of the three differentially expressed gene lists (OxLDL vs. control, native LDL vs. control and ELDL vs. control) are available in Supplementary Figs 4-6.

We next explored functional annotation cluster using DAVID tools v6.8 and Ingenuity pathway enrichment analysis. The top three canonical pathways for ELDL vs. control are activation of p38 MAPK, NFkB, ERK and is shown in Fig. 3a . We next measured activation of phospho ERK2, phospho p38 and NFkB/p65 in whole cell lysis extracts prepared from HCASMC stimulated with ELDL (10 μg/ml) or BSA as control. As shown in Fig. 3b , all three signaling pathways were significantly activated in ELDL-stimulated cells. Figure 3c presents the top canonical pathways affected by the list of Differentially Expressed Genes (DEGs) detected when comparing ELDL-treated smooth muscle cells versus control-treated smooth muscle cells. Each pathway is represented with its respective z-score, −log(p-value) and ratio. The calculated z-score indicates a pathway with genes exhibiting overall increased mRNA levels (orange bars), decreased mRNA levels (blue bars), no change (white bars), or no pattern available (grey bars). The calculated z-score is a statistical measure of the match between expected relationship direction and observed gene expression, if the z-score > 2 or <−2 it is considered significant by Ingenuity Pathway Analysis (IPA) tool. The ratio (orange dots connected by a line) indicates the ratio of genes from the dataset that map to the pathway, divided by the total number of genes that map to the same pathway. For ELDL-treated smooth muscle cells the top canonical pathways affected includes biological processes linked to cytokine activation (LPS/IL-1, IL17 signaling, IL-8 signaling), cell migration pathways (bladder cancer signaling, colorectal cancer signaling) and other (Fig. 3C) . With the exception of IL-8 and IL-17, none of those pathways reached significant threshold in HCASMC treated with OxLDL or native LDL. As for oxLDL, the top canonical pathway was DNA damage checkpoint regulation ( Supplementary Fig. 7) , and NRF2-mediated oxidative stress response was the top canonical pathway for native LDL (Supplementary Fig. 8 ).

Taken together, this suggests that ELDL has unique properties in modulating gene expression in HCASMC. Activation of p38 MAPK, NFkB and ERK signaling was identified in the bioinformatics analysis as the most significantly upregulated upstream regulators and this was verified in cultured cells using ELISA assays for those signaling kinases. Furthermore, Supplementary Fig. 9 shows the network of cardiovascular system development and function for ELDL-treated HCASMC and demonstrates several nodes related to SMC-differentiation and calcification as shown by the canonical pathways of "Role of Osteoblast, Osteoclasts and Chondrocytes in Rheumatoid Arthritis", "Role of Pattern Recognition Receptors in Recognition of Bacteria and Virus", and "Atherosclerotic Signaling". genes differentially expressed in ELDL-treated cells, Angiopoietin like protein 4 (ANGPTL4) was one of the most up-regulated genes in the microarray data with a 22-fold increase (Fig. 4a) . ANGPLT-4, MMP-3, MMP-10, bone morphogenic protein 2 (BMP2), and matrix gla protein (MGP) were validated by RT-PCR (Fig. 4b) .

Moreover, we found that ELDL induced a 20-fold upregulation of ANGPTL4 at 6 and 24 h, while OxLDL upregulated ANGPTL4 8-fold after 24 h, but not at the early time point of 6 h (Fig. 4d ). This demonstrates that ELDL is very potent in inducing ANGPTL4 mRNA. However, there was no difference in ANGPLT4 protein expression in HCASMC stimulated with ELDL or BSA as shown by semi-quantitative immunoblotting (Fig. 4c) .

ANGPTL4 mRNA is stimulated by fatty acids and may serve to protect cells against excess of fat uptake 27 . We therefore hypothesize that ELDL uptake potentially loads cells with lipids such as cholesterol and fatty acids and we tested whether lipid loading of HCASMC is required for up-regulation of ANGPTL4 mRNA. HCASMC were pretreated with lacidipine, a calcium channel inhibitor that was previously shown in our laboratory to abolish cellular uptake of ELDL in murine SMCs 7 . Similarly to murine SMCs, pretreatment of HCASMCs with lacidipine Fig. 4e . ANGPTL4 was originally identified as a PPAR α or γ induced protein 28, 29 , and it was shown later that ANGPTL4 is also induced by PPAR β/δ 27,30 . We next examined the effect of lacidipine on mRNA expression for ANGPTL4 and found significant reduction of ANGPLT4 mRNA in HCASMC treated with lacidipine and ELDL, but no effect on ANGPLT4 mRNA induced by bezafibrate, a PPAR agonist (Fig. 4f ). This suggests that ELDL uptake leading to foam cell formation is required for ELDL-mediated ANGPTL4 up regulation. ANGPTL4 up-regulation by ELDL is PPAR β/δ mediated. We further were interested in potential molecular mechanisms in ELDL-induced upregulation of ANGPTL4 in HCASMC. PPARs are regulators of lipid metabolism in cells, and unsaturated fatty acids are major ligands for all PPARs 31 and we speculate that ELDL could potentially load HCASMC with such fatty acids. We therefore investigated whether ELDL-induced upregulation of ANGPTL4 in HCASMC is a PPAR dependent phenomenon. Synthetic PPAR agonist, fenofibrate is both a PPAR α and γ ligand with 10-fold selectivity for PPAR γ, while bezafibrate is a pan PPAR agonist 31 . When HCASMC were incubated with either bezafibrate or fenofibrate at 100 μM for 24 h, only bezafibrate upregulates ANGPTL4 mRNA (25 fold, Fig. 5a ), indicating that ANGPTL4 mRNA upregulation in HCASMC is largely dependent on PPAR β/δ. To test this further, we employed several specific PPAR inhibitors and examined whether pretreatment with PPAR inhibitor attenuates ELDL-mediated increase in ANGPTL4 mRNA. Co-incubation of ELDL with GW6471, a specific PPAR α inhibitor did not change ANGPTL4 mRNA expression compared to that induced by ELDL alone (Fig. 5b) . Further, we incubated ELDL with specific inhibitors of PPAR γ (GW9660) or PPAR β/δ (GSK 0660) and found that only GSK 0660 inhibited ELDL-induced upregulation of ANGPTL4 (Fig. 5c ). This indicates that ELDL induced upregulation of ANGPTL4 is a PPAR β/δ dependent phenomenon. Moreover, PPAR β/δ inhibitor-GSK 0660 also inhibited upregulation of ANGPTL4 mRNA in cells co-incubated with OxLDL (Fig. 5d) , supporting the hypothesis that loading of HCASMCs with fatty acids mediates the increase ANGPTL4 mRNA in HCASMCs.

ELDL and rANGPTL4 induces migration in cultured human coronary artery smooth muscle cells. Growth factors, cytokines and extracellular matrix components promote migration of SMC in the atherosclerotic microenvironment within the vessel wall 22 . Modified LDLs are known to induce SMC migration and increased proliferation and migration of vascular SMC has been reported in response to OxLDL and ELDL 8,25,32 .

qRT PCR analysis of ANGPTL4 mRNA in HCASMC; all treatments were for 24 h and data are represented as mean ± SD; (a) HCASMC incubated with either control BSA or bezafibrate (100 μM) or fenofibrate (100 μM). **p < 0.01 for bezafibrate vs control BSA. (b) HCASMC incubated with either control BSA or 10 μg/mL ELDL ± GW6471 (25 μM, PPAR α inhibitor). **p < 0.01 for ELDL ± GW6471 vs control BSA. (c) HCASMC incubated with either control BSA or 10 μg/ mL ELDL ± GW9660 (10 μM, PPAR γ inhibitor) or 10 μg/mL ELDL ± GSK0660 (10 μM, PPAR β/δ inhibitor). **p < 0.01 for ELDL ± GW9660 vs control BSA and ELDL vs ELDL + GSK 0660. (d) HCASMC incubated with either control BSA or 25 μg/mL OxLDL ± GSK 0660(10 μM). **p < 0.05 for OxLDL vs OxLDL + GSK 0660.

HCASMC were incubated in dose-dependent manner with ELDL (0, 5 and 10 μg/ml) or OxLDL (40 μg/ml) for 24 h, after which cells (25000 cells in 100 μL media) were seeded on to the upper well of a transwell with an 8 μM porous membrane and cultured in media containing 20 ng/ml PDGF-BB in the lower well as chemoattractant. After 4 h in culture, cells on the upper side of the membrane were scrapped with a cotton swab, and the cells that migrated to the bottom side of the membrane were stained with crystal violet and subjected to quantification. As shown in Fig. 6a and quantified in b, ELDL upregulates migration of HCASMC, and is more potent than OxLDL. Since ELDL induces ANGPTL4 in HCASMC (Fig. 4) and ANGPTL4 promotes cell migration in experimental models of cancer 33,34 , we next tested whether recombinant ANGPTL4 protein stimulates migration of HCASMCs. We found that rANGPTL4 (5 μg/ml) significantly induces migration of HCASMC, and the effect was comparable to that by ELDL 10 μg/ml. Importantly, when HCASMC were co-incubated with ELDL and lacidipine (20 μM), migration of HCASMC was significantly reduced to basal levels indicating that ELDL uptake by the cells is necessary to induce migration in the HCASMC. In contrast, Lacidipine, did not influence rANGPTL4-induced migration of HCASMC (Fig. 6a,b ).

Next, we tested whether ANGPTL4 is required for ELDL-induced HCASMC migration and utilized siRNA ANGPTL4 and control siRNA (RNAiMAX, LifeTechnologies). ANGPTL4-siRNA reduced ANGPTL4 mRNA by more than 70% in ELDL-treated cells, indicating that the siRNA was highly functional in inducing a net reduction of ANGPTL4 mRNA levels in ELDL treated HCASMC (Fig. 6c) . However, siRNA mediated knockdown of ANGPTL4 mRNA in ELDL treated HCASMC did not prevent ELDL-induced HCASMC migration as shown in Fig. 6d ,e. This indicates that ANGPLT4 is not required for ELDL-mediated migration of HCASMC. Moreover, siRNA mediated knockdown of ANGPTL4 in ELDL-treated cells had no effect on MMP3 and MMP10 mRNA expression in ELDL treated HCASMC (Supplementary Fig. 10 ). Taken together, our results indicate that both ELDL and rANGPTL4 upregulates migration in cultured HCASMC, and ANGPTL4 acts downstream of ELDL but is not required for ELDL-mediated cell migration.

We examined the effect of native LDL, ELDL and OxLDL on proliferation of HCASMC using two different assays, the MTT Proliferation assay (MTS/Formazan conversion) and BRDU incorporation. We found that native LDL and ELDL had no significant effect on proliferation of HCASMC and proliferation was similar to control cells treated with BSA. In contrast, OxLDL inhibited cell proliferation by approximately 20% ( Supplementary  Figs 11 and 12 ).

ELDL upregulates phosphate induced calcification in cultured human coronary artery smooth muscle cells. Microarray gene expression profile of ELDL-induced HCASMC foam cells showed significant upregulation of mRNA for bone morphogenic protein 2 (BMP-2, ~ 2 fold), and downregulation of mRNA for matrix gla protein (MGP, >2 fold) as shown in Fig. 4a ,b. Since BMP-2 and MGP are important proteins involved in vascular calcification, with MGP having regulatory roles for BMP-2 mediated vascular calcification [35] [36] [37] [38] , and together with supporting data from the bioinformatics network analysis suggesting a role of ELDL for osteoblastic transformation as shown in Supplementary Fig. 9 , we examined whether ELDL promotes calcification of HCASMC using Alizarin Red stain. ELDL alone (10 µg/ml) or in combination with organic phosphate beta Glycerophosphate (10-30 mM) in regular cell culture medium did not promote Alizarin Red staining when cultured up to 7 days ( Supplementary Fig. 13 ), therefore inorganic phosphate at low concentrations from 0.5-1.5 mM was added to the cell culture medium to increase susceptibility to calcification. Consistent with previously reported findings 39 , we found no spontaneous calcification of HCASMC cultured in medium containing 0.5 and 1.0 mM phosphate. However, upon treatment with ELDL (5 μg/ml) to HCASMC cultured in medium containing 0.5-1.0 mM inorganic phosphate, there was significantly augmented mineralization of ELDL-treated cells as early as the 2 nd day of incubation (Fig. 7a) . A higher magnification is provided in Supplementary Fig. 14 . For quantification, the deposited Alizarin-Ca 2+ complexes were extracted and the OD of the suitably diluted samples was read at 570 nm and normalized to total cellular protein. ELDL-treated cells showed significant more calcification compared to control (BSA) cells and this was evident on day 2-4 and plateaued by the 5 th and 7 th day of incubation (Fig. 7a,b) . Since the effect was most noticeable at early time points, we tested the hypothesis that ELDL may alter gene expression of genes known to control osteogenic function in smooth muscle cells. mRNA was harvested from HCASMC cultured for 24 hours in the respective medium, at a time point without any morphological changes upon light microscopy nor increased Alizarin red staining. Moreover, there was no difference in mRNA quality and in the relative expression level for endogenous control genes HPRT and GAPDH (data not shown). Of the osteogenic genes known to be involved in vascular calcification, we selected genes either known to promote calcification (Dentin matrix acidic phosphoprotein 1, DMP-1; Alkaline phosphatase, ALPL; Runt-related transcription factor 2, RUNX2; Osteopontin, OPN/SPP1; osterix/SP7; BMP-2) or genes known as inhibitors of calcification (MGP, ectonucleotide pyrophosphatase/phosphodiesterase, ENPP-1) and measured their expression level by real time RT-PCR in HCASMC (Fig. 7c) . ELDL in 1 mM phosphate medium upregulates pro-calcifying genes (DMP-1: 2 fold; SPP1: 5 fold; SP7: 2 fold; and BMP-2: 5 fold) and there was no difference ALPL and RUNX2. Interestingly, MGP mRNA and ENPP1 were strongly reduced (47-fold and 3 fold, respectively) by ELDL in 1 mM phosphate medium. Taken together our result indicates that ELDL significantly augments phosphate-induced calcification in cultured HCASMC by altering osteogenic gene expression.

The importance of ELDL and its atherogenic potential is now recognized as equally important along with other modified forms of LDL such as OxLDL 14 . While many studies have focused on macrophages as the main cell type in contributing to intimal foam cells, it is also known that smooth muscle cells can transform into foam cells in vitro and in human atherosclerotic lesions 5,40-42 . Here we show that human coronary artery smooth muscle cells avidly take up ELDL, and very low amounts of ELDL were sufficient to promote foam cell formation. To our knowledge, this is the first report for quantitative comparison of ELDL with other modified LDLs in inducing foam cells in HCASMC. Normal and atherosclerotic intima has been shown to contain 2 to 4 times higher content of native LDL than that is in circulation 43 . Since plasma LDL concentration is ≈1 mg/mL, intimal fluid may contain 2 mg/ml of native LDL. In our invitro experiments, foam cell formation by native LDL at 2 mg/mL was similar in intensity to that by 200 μg/mL native LDL (data not shown), although significantly less in comparison to ELDL at 10 μg/mL. Although ELDL has been detected previously in atherosclerotic lesions in the vasculature and in calcific aortic valve disease in vivo [10] [11] [12] [13] , the concentration of ELDL in circulation is not known. Nevertheless, our invitro data suggests that ELDL is more potent than OxLDL or native LDL in inducing foam cells in cultured HCASMC.

In vivo, ELDL represents one of the many forms of modified LDLs that may form foam cells in macrophages and smooth muscles cells, and phenotypic modulations brought about by individual modified LDLs overlap significantly in an atherosclerotic milieu, making it practically impossible to differentiate between each other. By studying invitro-generated modifications of LDL we were able to demonstrate marked differences in the transcriptome of human SMCs upon uptake of ELDL, OxLDL and native LDL, indicating that specific modifications of LDL in the atherosclerotic plaques may determine the biology and functional consequences in vasculature.

We showed that MAPKp38, ERK and NFkB activation were the top three canonical pathways in an unbiased Ingenuity pathway enriched network analysis of ELDL-treated HCASMC, and these findings were confirmed by ELISA. This is in agreement with a recent study demonstrating co-localization of immunohistochemical staining for ELDL and p38MAK/MAPK14 in human carotid endarterectomy tissue from atherosclerosis with high grade stenosis 44 . Among the wide-ranging downstream activities of phosphorylated p38MAPK, cytokine production is a component related to atherosclerosis and osteoblast differentiation 45 . Indeed, biological network analysis indicates a potential role of ELDL in altering gene expression linked to calcification by (i) inhibition of calcification SCIentIfIC RepoRts | (2018) 8:11954 | DOI:10.1038/s41598-018-30073-w inhibitors, and by (ii) activation of osteogenic genes. To test whether ELDL promotes vascular calcification, we cultured HCASMC in phosphate-containing medium and found that addition of ELDL highly reduces gene expression of matrix gla protein and ENPP-1, together with up-regulation of other genes promoting calcification. Matrix gla protein is known as a major inhibitor of calcification 37, 38 . ENPP1 is an enzyme that converts extracellular ATP to adenosine and thereby generates pyrophosphate, an important inhibitor of hydroxyapatite formation and calcification. Recessive loss of function mutation in ENPP1 leads to loss of enzyme activity, and to infantile arterial calcification 46, 47 . The direct molecular mechanisms by which ELDL accelerates calcification of SMCs is not clear, but at least in part, it is linked to acquiring an osteoblastic gene profile in SMCs. Other lipoproteins including lipoprotein (a) and OxLDL have recently been shown to activate innate immune responses in interstitial valve cells leading to a gain of pro-calcific phenotypes in calcific aortic valve disease [48] [49] [50] .

Another important finding of our study is up-regulation of ANGPTL4 mRNA in HCASMC upon treatment with ELDL as demonstrated in the Illumina bead chip assay (22-fold increase) and confirmed by RT PCR. ANGPTL4 was recently shown to be expressed in murine coronary SMCs and cardiomyocytes in mice challenged with oral fatty acid bolus 30 , supporting the notion that our approach using in-vitro generated ELDL on cultured Supplementary Fig. 14) . (b) Quantification of -Ca 2 deposits from. Alizarin-Ca 2+ complexes were extracted by the addition of 1 ml of 10% CPC in water. This extract was further diluted 1:10 before the optical density was read at 570 nm. Data are represented as mean ± SD, *p < 0.05 for ELDL (day 2-6) vs control BSA. (c) qRT PCR analysis of osteoblastic gene mRNA in HCASMC incubated for 24 hours with either 10 μg/ mL ELDL or control BSA with 1 mM inorganic phosphate. Data are represented as mean ± SD, **p < 0.01 for ELDL vs control BSA in SPP1, BMP2 and MGP, *p < 0.05 for ELDL vs control BSA in DMP-1, SP7 and ENPP1.

SCIentIfIC RepoRts | (2018) 8:11954 | DOI:10.1038/s41598-018-30073-w HCASMC sufficiently models in vivo processes. ANGPTL4 is a strong inhibitor of lipoprotein lipase and thought to prevent lipid toxicity to fat-loaded cells 27, 30, 51 . Therefore, up regulation of ANGPTL4 mRNA in HCASMC in response to ELDL is possibly as a physiological response to prevent lipid toxicity. Other roles of ANGPLT4 include regulation of hematopoiesis and cell migration in keratinocytes and fibroblasts 52, 53 . However, while our data show induction of ANGPLT-4 mRNA in response to ELDL, we did not find an increase in ANGPLT4 protein level. Moreover, knockdown of ANGPLT-4 mRNA with siRNA did not prevent ELDL-mediated migration, suggesting that ANGPTL4 is not required for migration of HCASMC. ANGPTL4 has been studied in murine atherosclerosis. One study reported on decreased atherosclerotic lesion size in ApoE3-Leiden mice with transgenic overexpression of ANGPTL 4 30,54 , while Aryal et al. showed decreased atherosclerosis in LDLR null mice with global knock out of ANGPTL4 and accelerated atherosclerosis in LDLR null mice lacking ANGPTL4 only in the hematopoietic cells 55 . This suggests that ANGPTL4 has tissue specific effects with regards to atherosclerosis and our finding of enhanced migration of HCASMC by rANGPTL4 supports a pleotropic role of ANGPTL4 in regulation of non-metabolic processes.

Furthermore, coding variations in the ANGPTL4 gene has been studied in human populations, and for example a loss-of-function allele E40K in ANGPTL4 was associated with protection for myocardial infarction in the CARDIoGRAM exome consortium 56 , although associated with increased risk in another study 57 .

Lastly, we demonstrate that lacidipine attenuates uptake of ELDL in HCASMC. Lacidipine is a calcium channel blocker with antioxidative properties and we showed previously that it inhibits macropinocytosis of ELDL in a calcium and oxidative stress-dependent manner in murine SMCs 7,58 . We speculate that blocking ELDL-mediated foam cell formation of HCASMCs could be a potential therapeutic target for atherosclerosis. This hypothesis is supported by findings from a clinical trial, in which lacidipine (compared to atenolol) was shown to decrease carotid atherosclerosis in the European Lacidipine Study on Atherosclerosis with a greater efficiency on carotid intima-media thickness and number of plaques per patient despite a smaller reduction in ambulatory blood pressure, suggesting that the anti-atherogenic action of lacidipine is independent of its anti-hypertensive action 59 . A better understanding of these processes may lead to potential therapeutic options to inhibit ELDL uptake and smooth muscle foam cell formation.

In summary, we demonstrate that stimulation of HCASMC with ELDL promotes a "pro-atherosclerotic" phenotype by transforming smooth muscle cells into foam cells, associated with enhanced migration and gaining of osteoblastic gene expression. We speculate that this process could play a role in vivo since ELDL has been identified in atherosclerotic vasculature. Our data support the hypothesis that uptake of ELDL by SMCs could potentially lead to translocation of SMCs with altered phenotype, and by gaining of an osteoblastic gene profile may promote development of micro-calcification foci in SMC-rich areas of atherosclerotic plaques.

Lipoprotein Isolation and Modifications. LDL, ox LDL and ELDL was prepared as described previously by us 7 . Briefly, human plasma LDL (density 1.02-1.063 g/ml) was isolated by preparative ultracentrifugation under sterile conditions. To generate OxLDL, human LDL (5 mg) in 1 ml PBS containing CuSO4 (10 μM) was incubated for 48 h at 37 °C. The oxidized LDL was then dialyzed against PBS extensively, filter sterilized and stored at 4 °C. Protein content was measured by Bradford method. To generate Enzyme modified LDL (ELDL) 1 mg LDL was digested with 2 μg trypsin (Sigma) and 12 μg cholesterol esterase (Sigma) and incubated at 37 °C for 16 h, followed by adding another 2 μg trypsin and 20 μg cholesterol esterase per mg LDL cholesterol and incubation for 48 h at 37 °C. At the end of the incubation, the ELDL preparation looked cloudy and was extensively dialyzed (molecular weight cut off = 100 KD) against PBS. ELDL was filter sterilized and stored at 4 °C. Protein content was measured by Bradford method. ELDL was tested for trypsin content using trypsin activity assay kit (Abcam) and found to be similar to original LDL. Moreover, LDL and modified LDL's were tested for endotoxin using the PYROGENT gel clot LAL assay (Lonza) and only negative samples were used for experiments.

HCASMC were purchased from Life technologies and cultured according to manufactures recommendation in Medium 231 supplemented with smooth muscle growth supplement (GIBCO). As per manufacturer information, cells were isolated by the enzyme digestion method as previously described by Ray et al. 60 . Expression of αSMA, a specific adult SMC marker, and absence of the specific endothelial cell protein CD31 was confirmed in HCASMC by immunoblotting using anti human SMA IgG (abcam) and anti human CD31 IgG (RD systems). As control cell line we used Human Aortic Endothelial cells, which abundantly express CD31 and was a kind gift by Dr.Yun Fang, Section of pulmonary and critical care, Department of Medicine, University of Chicago ( Supplementary Fig. 15 ). Three different batches of HCASMC (from Life technologies) were propagated and passage 2-7 were used for experiments. With the exception for the microarray experiment, which was performed on HCASMC from only one donor, all other experiments utilized three different batches of HCASMC and each cell line was tested in triplicates.

were cultured on 18 mm cover glass slips in 12-well dishes in media M231 supplemented with SMGS (SMC growth supplements, Life technologies) and 1% antibiotic-antimycotic (Gibco). BSA (control), native LDL, copper oxidized LDL or ELDL was added to cells in indicated dosages and incubated for 24 h at 37 °C. Where indicated, calcium channel inhibitor-lacidipine (Sigma) was added to the cells 1 h before the addition of ELDL for the entire incubation period of ELDL. Foam cell formation was assessed visually by Oil Red O staining intensity and quantified as a function of total cholesterol/protein in the cells.

Oil Red O staining. 0.35 g of Oil Red O (Sigma) was dissolved in 100 ml of isopropanol and stirred overnight at room temperature. Prior to use, the solution was filtered followed by dilution with water (volume 6:4) and

SCIentIfIC RepoRts | (2018) 8:11954 | DOI:10.1038/s41598-018-30073-w filtered again immediately before applying to cells. Adherent cells were rinsed with PBS and fixed in 10% formalin at room temperature for 1 hour followed by rinsing with water. The cells were then incubated in 60% isopropanol for 5 minutes at room temperature and drained off. After complete drying of the cells, staining with Oil Red O for 10 minutes at room temperature was performed. The Oil red O was then removed and the cells were immediately rinsed with water 4 times. Cells were cover-slipped with mounting medium and the images were acquired with a light microscope at 600 X magnification.

Whole genome gene expression and bioinformatics. HCASMC were cultured and stimulated with 50 μg/ml cholesterol (native LDL, ELDL, OxLDL) or bovine serum albumin for 24 hours. mRNA was harvested and 12 samples (three biological triplicates from 4 different treatment groups) were submitted to the Genomics Facility at the University of Chicago. Whole genome gene expression was profiled by microarray chips using the Illumina BreadChip HT-12v4 array. Bioinformatics analysis was performed at the Bioinformatics Core, Center for Research Informatics. Briefly, raw microarray data were processes by Illumina Genome Studio v2011.1 and Partek Genomics suite v6.6. Average signal intensities were background-subtracted, log2 transformed, and quantile normalized. A total 47,323 processed intensities and associated detection p-values at the probe level were obtained. The processed intensities at probe level were further filtered by detection p-value ≤ 0.01 in at least 3 samples. After filtering, 17,903 processed average signal intensities at probe level were used for the detection of differentially expressed genes (DEGs). Statistically significance for the DEGs was defined by the cut off of absolute value of fold change >1.5, and false discovery rate corrected p-value < 0.05. Detected differentially expressed genes and were further used for function annotation clustering analysis using DAVID tools v6.8 Beta and Ingenuity Pathway Analysis (IPA)". Western Blots. Protein expression was semi-quantified by western blotting in whole cell lysis extracts from HCASMC using anti human ANGPTL4 antibody (abcam, ab115798), anti human CD31 IgG(RD systems), and anti human aSMA IgG (abcam).

ELISA. phosphorylated ERK2, p38α and NFκB/p65 activity in HCASMC treated with ELDL or control were measured in whole cell lysis extracts using ELISA kits as per manufacturer's instructions (ERK2 and p38α kits from RD sytems, NFκB/p65 kit from Novus biologicals). Cells were treated with 10 µg/ml ELDL for 4 hrs, BSA incubated cells were control.

Quantitative real-time RT-PCR. Cells were preincubated with pharmacological agents such as Bezafibrate (100 µM), Fenofibrate (100 µM), GW 6471 (25 µM), GW 9660 (10 µM) and GSK 0660 (10 µM) (all Sigma) prior to adding modified LDLs as indicated. RNA was isolated from cells using TRIzol reagent (Invitrogen). First-strand cDNA was generated from 3 µg RNA using Superscript III (Invitrogen) and random primers (Invitrogen). Subsequently, the cDNA was diluted 1:10 and 2 µl cDNA was subjected to quantitative real time PCR using SYBR Green with a IQ5 cycler (BioRAD) with specific primers. All PCR amplifications were carried out in triplicates. The primers sequences are listed in Table 1 . The ΔC T value was used to describe the difference between the test and control cells normalized to the housekeeping gene HPRT. Relative mRNA expression was estimated as 2exp (ΔC T target gene-ΔC T housekeeping gene). There was no significant difference in absolute C T values for the amplification of HPRT among the different experimental groups (C T ranging from 19.59-20.52), indicating that RNA quality and abundance of this house keeping gene was not affected by the experimental design. si RNA mediated knockdown of ANGPTL4 was achieved using ANGPTL4 silencer RNA and control siRNA (Life Technologies). siRNA (25 pmole/2 ml/6well) was complexed with RNAiMAX(Life technologies) and added to cells as per manufacturer's instruction. The end point ANGPTL4 mRNA expression was measured by qPCR.

In vitro cell migration analysis. Human coronary artery smooth muscle cells (HCASMC) were cultured regularly in M231 media supplemented with SMGS. In invitro-cell migration analysis was performed by a modified method from that originally explained by Law et al. for cell migration towards a PDGF gradient 61 . Briefly, 50 ul of 1% complete growth media containing 20 ng/ml recombinant human PDGF-BB (BioLegend) was taken in a tissue culture well (12 well, Falcon) and a 8 µM transwell insert (Corning, transparent PET) was gently placed on to it. 25000 cells in 100 µl of 1% complete growth media were then placed in the transwell and cultured for 4 hrs. The cells were then gently scrapped off from the upper chamber/side of the transwell membrane using Q-tips (cotton swabs) and the transwell (with cells on the lower side of membrane) were fixed overnight in 10% formalin. Fixed transwells/cells were gently rinsed twice in distilled water and incubated for 15 minutes in 0.5% crystal violet in 25% methanol solution. Crystal violet was dissolved in methanol (100%) and then diluted with water to a final 25% methanol and solution was stirred for 15 minutes and filtered before adding to cells. Cells were washed several times gently using tap water until membranes are clear of background. Transwells were dried completely and the membranes were cut out from the transwell with a blade and assembled on a glass slide for microscopy.

In vitro calcification assay. Human coronary artery smooth muscle cell (HCASMC) were cultured in calcification medium according to procedure modified from Shioi et al. 62 . Cells between passages 3 and 7 were used from three different batches of HCASMC (Life Technologies). Cells were grown to confluency in 12 well dishes using human SMC culture media (medium M231 supplemented with SMGS, both from Life technologies). The cells were then washed with PBS, and incubated overnight with Advanced MEM (Life technologies) supplemented with 0.2% of FBS, 1X antibiotic antimycotic (Anti Anti-Life technologies, Gibco). The next day, the medium was replaced with pro-calcifying medium (Advanced MEM with 0.2% of FBS, 1X antibiotic-antimycotic containing 0.5-1.5 mM of inorganic phosphate. Regular Advanced MEM medium contains 1 mM phosphate. As indicated, 2.5-5 µg/ml of either ELDL or control BSA was added and cells were cultured for up to 6 days with 0.5% FBS added every day. Cells were fixed by air drying at room temperature, calcium deposits were visualized by staining with Alizarin Red S. Before use, the pH of Alizarin Red S solution (2% w/v in distilled water) was adjusted to 4.1-4.4 using 10% NH4 OH. Fixed cells were stained with Alizarin Red S solution for 10 minutes and washed 3 times with distilled water to remove unbound stain. Quantification of the calcium-alizarin complexes were done according to a method described by Prosdocimo et al. 63 . Briefly, the deposited Alizarin-Ca 2+ complexes were extracted by the addition of 1 ml of 10% CPC in water. This extract was further diluted 1:10 before the optical density was read at 570 nm.

Human coronary artery smooth muscle cell proliferation. HCASMC at 3000 cells/ml were seeded into a 96 well plate. At indicated time points (24, 48, 72 and 120 h), MTS (3-(4,5-dimethylthiazol-2-yl)-5-(3-ca rboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) was added according to the manufacture's protocol (Biovision, non-radioactive cell proliferation assay) and cells were incubated for 45 min. The reduction of MTS by the cells into a formazan product was measured directly at 590 nm using an Elisa plate reader (Fluostar, BMG labtech). For BrdU incorporation, cells (3000 cells/ml) were seeded onto glass cover slips and grown for 24 hours, and cells were pulsed with 10 μM BrdU (Sigma Aldrich) for 3 hours followed by detection of BrdU incorporation using anti BrdU monoclonal antibody (BD Biosciences) according to the manufactures. Nuclei were stained with DAPI. All nuclei and BrdU positive nuclei were counted on ten high power fields by a blinded investigator using a fluorescence microscope.

All experiments were performed in triplicates and repeated two times. With the exception for the microarray experiment, which was performed on HCASMC from only one donor, all other experiments utilized three different batches of HCASMC (from Life technologies) and each cell line was tested in triplicates. Results are presented as mean ± standard deviation. Statistical differences were analyzed using independent sample T-test and one-way analysis of variance were used for mean comparison between two or multiple groups, respectively. Two-tailed probability values of p less than 0.05 were considered statistically significant for each test to ensure an overall study significance level of P < 0.05.

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This study was supported by the National Health Lung and Blood Institute (1R01HL4821 to M.A.H.B.) and the NIDDK STEP-UP program to E.R. All experiments on primary human coronary artery smooth muscle cells were performed with commercially available cell lines from unidentified donors as described in the methods section, and performed in accordance with relevant guidelines and regulations and approved by the Institutional Biosafety Committee of the University of Chicago.

Bijoy Chellan performed experiments, analyzed the data and drafted the manuscript. Elizabeth Rojas performed proliferation assay on HCASMC. Chunling Zhang performed micro array experiments and bioinformatics analysis. Marion Hofmann Bowman performed experiments, analyzed data and edited the manuscript. Drs. Chellan and Hofmann Bowman have contributed equally to the work and have jointly supervised the work. All authors have read the manuscript and agree with the data and findings.

Supplementary information accompanies this paper at https://doi.org/10.1038/s41598-018-30073-w.

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