Identifcation And Functional Analysis Of A Bifavone As A Novel Inhibitor Of Transient Receptor Potential Vanilloid 4‑dependent Atherogenic Processes

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Mazen O.Alharbi, Bidisha Dutta, RishovGoswami, Shweta Sharma, Kaye. Lei &Shaik O. Rahaman

Atherosclerosis, a progressive inflammatory disease of large arteries, constitutes the foremost contributor to the growing burden of cardiovascular disease-related mortality and morbidity globally1. Te pivotal initiating event that leads to atherosclerosis involves retention of modified low-density lipoprotein (oxLDL) particles in the subendothelial aortic intimal spaces primarily in arterial branch points2. During early atherogenesis, following endothelial dysfunction, circulating blood monocytes transmigrate into the intima areas, and differentiate into tissue macrophages3. In aortic intimal spaces, binding and uptake of oxLDL by macrophages aided by scavenger receptors like SRA and CD36 creates a feedforward athero-inflammatory loop resulting in the development of lipid-laden foam cells, a critical process in atherosclerosis2–8. The Cascades of the-inflammatory events provoked by foam cells lead to the formation of an early fatty streak and eventually the appearance of advanced atherosclerosis lesions characterized by the presence of fibrous cap, calcified tissue, immune cells, matrix proteins, and lipids2–10. Transient Receptor Potential Vanilloid 4 (TRPV4) of the TRPV subfamily, a non-selective, polymodal cation channel permeable to Ca2+ is ubiquitously expressed in various cell types including macrophages11–24. Previously known as an osmosensor, TRPV4 is now known to respond to multifarious biochemical and biomechanical stimuli including heat, matrix stiffness, osmolarity, growth factors, pH, and 4α phorbol esters11–24. TRPV4 is reported to mediate several physiological functions like pain sensation in inflammation and neuropathies18,22,23, myofibroblast differentiation and migration 17,25,26, and osteoclast differentiation in the bone27. TRPV4 mutations have been associated with several channelopathies28–31. Recent studies by our group and others have implicated a possible role of this channel in myriad pathological conditions like lung injuries22,32, foam cell formation14,16, tissue fbrosis17,33, foreign body response13, and cancer34,35. Previously, an atheroprotective role of TRPV4 was shown, in which chemical agonist-induced TRPV4 function in endothelial cells was shown to be associated with activation of eNOS and inhibition of monocyte adhesion to endothelial cells36. In contrast, deficiencies in TRPV4 functions have been linked to numerous atheroinfammatory responses including endothelial dysfunction, reduced macrophage foam cell generation, and vascular diseases14,16,37–39. Our laboratory has recently identified a proatherogenic role of TRPV4 whereby it regulates oxLDL-induced macrophage foam cell formation. Mechanistically, we showed that TRPV4 affects the uptake but not binding of oxLDL in macrophages in a CD36-independent manner14. In another study, we reported a TRPV4-dependent exacerbation of oxLDL-induced foam cell formation in the presence of lipopolysaccharide and increasing matrix stiffness, thus providing a link between mechanosensing and risk of atherosclerosis16. Considered all together, these findings suggest TRPV4 as an attractive target in atherosclerosis and other diseases, thus incentivizing the discovery of small molecule inhibitors of TRPV4 that can be translated into clinically effective therapeutics. The uses of natural compounds in therapeutics have gained prominence, primarily driven by the need for cost-effective and biocompatible compounds as compared to the currently existent synthetic drugs. Natural compounds such as flavonoids, alkaloids, polyphenols, and curcuminoids, affect cardiovascular diseases via diverse mechanisms such as inhibition of proinflammatory signals, insulin sensitization, and improving blood lipid profiles by targeting the AMPK, COX1/2, eNOS, and Nrf2 pathways40–45. Recent studies by multiple groups have identified two flavonoids, berberine, and apigenin, as potential modulators of TRPV4 activity46,47. We have developed and used a semi high-throughput screening method to identify potential antagonists of TRPV4 from a library of natural compounds using a Fluorometric Imaging Plate Reader (FLIPR) -based Ca2+ influx assay. Herein, we report the identification and functional analysis of Linkedin, a flavone, as a novel inhibitor of TRPV4-dependent atherogenic processes in macrophages, thus laying a foundation for further studies of this natural compound as a natural anti-atherosclerotic small molecule compound. Linkedin has been reported to display neuroprotective, anti-carcinogenic, and anti-inflammatory roles48,49. We report the mechanism of action of Linkedin against TRPV4 in the setting of macrophage foam cell formation using numerous biochemical and cellular assays.

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Materials and methods Animal and cell culture

We purchased congenic C57BL/6 wild type (WT) mice from Charles River Laboratories (Wilmington, Massachusetts, USA). University of Maryland Animal Care and Use Committee guidelines were followed for all animal experiments and the authors complied with ARRIVE guidelines. For isolation of thioglycolate-induced murine resident macrophages (MRM), peritoneal lavage was collected after 4 days of intraperitoneal thioglycolate injection, and cells were maintained in 10% fetal bovine serum (FBS) containing DMEM7,14,16. A murine macrophage cell line (RAW264.7), and human dermal fibroblasts (HDF) were purchased from ATCC (Manassas, VA), and were cultured, respectively, with DMEM or MEM (Gibco, Waltham, MA). Murine bone marrow-derived macrophages (BMDMs) were harvested from 6- to 7-week old mice, as previously described14,50,51. Briefly, femurs from WT and TRPV4 KO mice were collected, and bone marrow of femurs was flushed out with complete DMEM media with 10% FBS. Te suspended bone marrow cells were filtered through a 70 µm strainer (BD bioscience), centrifuged, and maintained in DMEM medium supplemented with M-CSF (25 ng/mL) for 7–8 days at 37 °C to allow differentiation into macrophages.

Reagents

Linkedin and GSK1016790A (GSK101) were purchased from Sigma-Aldrich (St. Louis, MO), and the FLIPR Calcium 6 assay kit was obtained from Molecular Device (Sunnyvale, CA). Human native LDL (VLDL) was purchased from Stemcell Technologies (Vancouver, Canada). We incubated LDL with 5 µM CuSO4 for 12 h at 37 °C to prepare copper-oxidized LDL (oxLDL)7,14,16. Fluorescent dye-labeled, DiI-oxLDL, was purchased from Invitrogen (Carlsbad, CA), and MCSF from R&D (Minneapolis, MN). Antibodies for FACS analysis were: TRPV4 (Millipore; Burlington, MA), CD36 (R&D; Minneapolis, MN), TLR4, and TLR6 (Novus Biologicals; Centennial, CO). PE-conjugated secondary antibodies were from R&D (Minneapolis, MN), and PE-conjugated isotype controls were from BD (Franklin Lake, NJ). For quantitative polymerase chain reaction (qRT-PCR), we used the RNeasy kit from QIAGEN (Redwood City, CA). All primers were purchased from Bio-Rad (Hercules, CA). Cell culture media, cell culture-related products, and western blot reagents were obtained from Thermo Fischer Scientific (Waltham, MA).

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Semi high‑throughput screening

We undertook a semi high-throughput screening for antagonists of Trpv4 from a library of 2000 natural compounds (MSSP-2000, Johns Hopkins Chemcore) using a fluorometric imaging plate reader (FLIPR)-based calcium influx assay14,17. We identifed ginkgetin (GGT), as a novel antagonist to TRPV4. The primary and secondary screening was performed with RAW264.7, HDF, and BMDMs to assess the ability of Linkedin and other candidates to inhibit TRPV4-elicited Ca2+ infux14,17. As controls, we used A23187, a calcium ionophore, TRPV4 null BMDMs, and GSK219, a selective TRPV4 antagonist17. After the secondary screening, we identified six compounds showing more than threefold inhibition of TRPV4-mediated Ca2+ influx compared to vehicle control. Linkedin was identified as the most potent inhibitor of TRPV4 activity. BMDMs (5× 104 cells/well) were seeded into collagen-coated (10 µg/ml) 96-well clear bottom black plates and incubated at 37 °C, 5% CO2. On the day of the experiment, cells were loaded with calcium 6 dye in HBSS, 20 mM HEPES, 2.5 mM probenecid and incubated for 45 min at 37 °C. After incubation, library compounds were added to each well to a final concentration of 2 µM. Plates were incubated for another 45 min at 37 °C. Ca2+ influx was induced by the addition of 10 nM of TRPV4 agonist GSK1016790A in vehicle- or compound-pretreated cells and recorded by measuring ΔF/F (Max-Min), as previously described17. Data are shown as relative fluorescence units (RFU).

Immunoblots

Thioglycolate-elicited peritoneal macrophages were seeded in 10% FBS containing DMEM and incubated overnight. Unadhered cells were washed of, and 1% bovine serum albumin (BSA) containing DMEM was added to the plate and incubated for 3 h before Linkedin treatment. To determine the expression of CD36, TRPV4, TLR2, TLR4, TLR6, and GAPDH proteins whole-cell lysates were prepared from cells treated overnight with Linkedin (1 and 5 µM) or vehicle in the presence or absence of oxLDL (25 µg/ml). To determine the expression levels of LPS-triggered p-JNK and JNK, cells were pretreated with Linkedin (5 and 10 µM) for 3 h and then stimulated with E. coli LPS for 30 min. Whole-cell lysates were prepared from twice-washed cells (ice-cold PBS) using RIPA buffer with added protease inhibitor cocktail (Thermo Scientific, MA). Blots were probed with rabbit anti-TRPV4 (Alomone Lab, Jerusalem, Israel), anti-mouse CD36 (R&D, Minneapolis, MN), rabbit anti-TLR4, rabbit anti-TLR6, rabbit anti-JNK, and rabbit anti-p-JNK primary antibodies (Cell Signaling, Danvers, MA) followed by anti-rabbit and anti-mouse HRP-conjugated secondary antibodies (R&D, Minneapolis, MN). Blots were stripped and re-probed with anti-GAPDH IgG (1:2000; Santa Cruz, Dallas, TX) for loading control.

Foam cell formation. Thioglycolate-triggered MRM were seeded on glass coverslips in a 12 well plate with DMEM, 10% FBS and incubated at 37 °C, 5% CO2 for 2 h. GGT (1 or 10 µM) was added to the cells, and after 3 h of incubation, oxLDL (50 µg/ml) was added, and cultures were incubated overnight at 37 °C. Native LDL (50 μg/ml) was added to control group wells and incubated overnight. Cells were fixed in 4% paraformaldehyde followed by Oil Red O staining to quantify foam cell generation.

Adenovirus vector transduction. We collected Adenovirus constructs to express Ad(RGD)-mouseTRPV4 (Ade-TRPV4; ~1010 pfu/ml), and adenovirus blank vector, Ad(RGD)-CMV-null (Ade-Vec; 1011 pfu/ml), from Vector Biolabs, Malvern, PA. We used 1× 108 pfu/ml for all experiments. For foam cell generation studies, mouse peritoneal macrophages were incubated with Ade-TRPV4 or Ade-Vec in DMEM media for 72 h before the addition of oxLDL to generate macrophage foam cells.

Binding and uptake of ox-LDL. To assess binding, peritoneal macrophages were treated with two doses (1 or 10 µM) of Linkedin or vehicle for 3 h and incubated with DiI-oxLDL at 4 °C for one hour. After pre-treatment with Linkedin or vehicle, cells were incubated with DiI-oxLDL at 37 °C for 30 min to assess uptake. Images were captured by fluorescence microscopy (63x), and Image J was used to quantify results.

Flow cytometry analysis. Thioglycolate-elicited peritoneal macrophages were cultured in DMEM, 10% FBS for 24 h. Unadhered cells were washed off, serum-free medium was added, and cells were incubated for 2 h followed by the addition of 5 µM GGT or vehicle, and incubation was continued for 3 h. Treated cells were scraped off the plate and resuspended in PBS, 2% BSA. Cells were incubated with primary antibodies for 45 min followed by 30 min incubation with PE-conjugated secondary antibody. A FACSCantoII flow cytometer (BD Bioscience, Ontario, Canada) was used to acquire data. All data were processed using FlowJo software.

qRT‑PCR. Thioglycolate-induced macrophages were treated with 5 µM Linkedin or vehicle for 3 h; 25 µg/ ml of oxLDL were added to the vehicle or Linkedin-treated cells, and incubation was continued overnight. RNeasy Micro Kit (#74,004) from QIAGEN was used to extract total RNA, and a Universal SYBR Green One-Step Kit from Bio-Rad was used to reverse transcribe the RNA. A C1000 Touch Thermal Cycler (Bio-Rad) was used to acquire data. Expression of a gene was determined as the amount of gene-specific mRNA relative to GAPDH mRNA using the comparative CT method described in the Bio-Rad qRT-PCR system user bulletin.

Statistical analysis. Data are presented as mean±SEM of biological triplicates. GraphPad Prism 7.0 software was used, and calculations were conducted using Student’s t-test for two groups or one-way ANOVA for multiple groups.

Ethical approval. All experiments on mice were conducted in accordance with the Institutional Animal Care and Use Committee (IACUC) guidelines and were approved by the University of Maryland‐College Park Review Committee.

Results in Semi high‑throughput screening for antagonists of TRPV4 from a library of natural compounds using a FLIPR‑based Ca2+ influx assay. A library containing a collection of structurally and functionally known natural compounds was screened using a semi high-throughput FLIPR-based Ca2+ influx assay (Fig. 1A) to investigate the modulatory effect of these compounds on TRPV4-elicited Ca2+ influx. Initial screening performed with 2000 compounds on primary human dermal fibroblasts and RAW264.7 cells identified 76 lead compounds that significantly (≥threefold) inhibited GSK101-induced (a TRPV4 specific agonist) Ca2+ influx. We performed a secondary screening of the lead compounds using the same assay on RAW 264.7 cells. We further verified and selected 6 compounds that produced reproducible and significant (>threefold; p<0.001) inhibition of TRPV4-elicited Ca2+ influx in BMDMs as compared to the vehicle control (Fig. 1B). Our screening assay proved to be a high confidence assay for detecting small molecule compounds with TRPV4 inhibitory effects as reflected by a good Z factor value (0.703). We have used A23187 (A23), a calcium ionophore, as the positive control, and GSK2193874 (GSK219), a selective small-molecule chemical inhibitor of TRPV4, as the negative control14–17. Linkedin (GGT) was identified as one of the most potent inhibitors of TRPV4 in the screening. Since previously published reports showed that GGT has an anti-inflammatory and anti-adipogenic effect, we selected GGT for further functional analysis on TRPV4-dependent macrophage proatherogenic activity48,49,52,53.

Figure 1. Semi high-throughput screening-based identification of Linkedin as a novel TRPV4 inhibitor from a library of natural compounds. (A) Flow chart showing the workflow resulting in the identification of ginkgetin as a potential TRPV4 inhibitor from a library of 2000 natural compounds. (B) Representative FlexStation 3 recording showing the inhibitory effect of 6 natural compounds on TRPV4 agonist (GSK1016790A)-induced Ca2+ influx in calcium 6 dye-loaded BMDMs during secondary screening. Pretreatment with all 6 compounds showed inhibitory effects on TRPV4-dependent Ca2+ influx compared to cells pretreated with vehicle (negative control; vehicle plus GSK1016790A (10 nM)) or calcium ionophore (A23187, 2 μM). We used selective TRPV4 antagonist, GSK2193874 (10 nM), as a negative control. All experiments were repeated three times in quadruplicate. RFU: relative fluorescence unit.

TRPV4 inhibition by GGT abrogates oxLDL‑induced macrophage foam cell formation. Our previous studies showed that TRPV4-elicited Ca2+ influx is involved in oxLDL-mediated foam cell formation 14,16. Therefore, we evaluated the possibility that foam cell formation was inhibited by GGT-mediated antagonization of TRPV4 activity. Wild-type murine peritoneal macrophages were incubated with oxLDL to induce foam cell formation in the presence or absence of GGT, and analyzed by Oil Red O staining. As expected, we found that the generation of foam cells increased by fivefold in oxLDL treated macrophages in comparison to native LDL (Fig. 2A, B). However, treatment of the macrophages with GGT (1 or 10 µM) prior to stimulation with oxLDL significantly decreased the percentage of foam cells (Fig. 2A, B). Collectively, these findings suggest an inhibitory effect of GGT on macrophage foam cell formation possibly targeting TRPV4-elicited Ca2+ influx. Furthermore, we overexpressed TRPV4 in TRPV4 null macrophages by using adenovirus construct and then induced foam cell formation by using oxLDL in the presence of GGT. We found that overexpression of TRPV4 increased the foam cell formation which was blocked when we pretreated the cell with GGT, suggesting that inhibition of the proatherogenic foam cell formation by GGT is TRPV4 dependent (Fig. 2C, D).

GGT does not block the basal level of expression of TRPV4 and inflammatory receptors. Scavenger receptor CD36 plays a major role in the uptake and binding of oxLDL, and foam cell formation, critical processes in atherosclerosis4–7,54,55. Recently, a growing body of evidence suggests the involvement of toll-like receptors in atherosclerosis2,4,56. To investigate whether GGT blocked foam cell formation via affecting the expression of CD36, TLR4, TLR6, and TRPV4, we performed immunoblot analysis at two concentrations of GGT (1 or 5 µM). We found similar expression levels of CD36, TRPV4, TLR6, and TLR4 as compared to the untreated control (Fig. 3A–D). Flow cytometric analysis also revealed no significant difference in the cell surface expression of the proteins with or without GGT treatment (Fig. 3E–H, I–L). Considering all together, these results suggest that GGT blocks macrophage foam cell formation without inhibiting the basal levels of surface expression of TRPV4, CD36, TLR4, and TLR6.

Figure 2. Inhibition of TRPV4 by Linkedin abrogates oxLDL-induced macrophage foam cell formation. (A) Thioglycolate-induced murine peritoneal macrophages were treated overnight with 50 µg/ml oxLDL, followed by a 3 h preincubation with vehicle or 1 or 10 µM Linkedin. Cells were treated with 50 µg/mL native LDL (VLDL) as control. Original magnification: 40x. (B) Quantification of the results is shown in (A). n=500 cells/condition. Student’s t-test; ***p<0.001. Data represent±SEM. (C) TRPV4 KO RPMs were transduced with either Ade-Vec or Ade-TRPV4 and were untreated or treated with GGT in the presence of oxLDL for 16 h on day 5 of transduction for macrophage foam cell formation. (D) Quantification of the results shown in C. n=100 cells/condition. Student’s t-test; ***p<0.001.

Uptake of oxLDL, but not binding by macrophages is suppressed by GGT. Because TRPV4 has been previously shown to have a role in the uptake of oxLDL and foam cell formation14,16, we evaluated whether treatment with GGT caused impairment in the binding of oxLDL on the macrophage surface. WT peritoneal macrophages were treated with GGT prior to incubation with DiI-oxLDL at 4 °C, and binding was assessed. The results indicate that the binding of oxLDL on the macrophage surface was not significantly impeded by GGT (1 or 10 µM) treatment compared to vehicle control (Fig. 5A–C). Having established that GGT does not inhibit the binding of oxLDL, we next aimed to determine if uptake of oxLDL in macrophages was impaired by GGT treatment. Interestingly, our results indicated that there was significant inhibition in the uptake of oxLDL in macrophages in GGT pretreated cells as compared to the vehicle-treated group (Fig. 6A, B). Considering all together, these results suggest that GGT blocks the uptake of oxLDL, but not binding, in macrophages.

GGT blocks oxLDL‑induced expression of TRPV4 in macrophages.

As our previously published studies showed that TRPV4-elicited Ca2+ plays a role in oxLDL-mediated macrophage foam cell formation14,16, we sought to determine if GGT blocked foam cell formation via suppression of oxLDL-induced expression of CD36, TLR2, TLR4, TLR6, or TRPV4. We found that overnight stimulation of macrophages with oxLDL resulted in signifcant upregulation of the expression of TRPV4 proteins compared to LDL, while expression of other receptors (CD36, TLR2, TLR4, and TLR6) remained unchanged (Figs. 4A–F). Pretreatment of cells with GGT prior to stimulation with oxLDL selectively decreased the level of expression of TRPV4 proteins compared to vehicle treatment (Fig. 4A–F). Collectively, these findings suggest an inhibitory effect of GGT on TRPV4 protein expression, which may be in part involved in the suppression of foam cell formation by GGT.

Figure 3. Linkedin treatment does not alter the total protein or surface expression of TRPV4, CD36, and TLRs in macrophages. (A–D) Immunoblots of macrophage whole cell lysates following overnight treatment with 1 or 5 µM Linkedin or vehicle. Representative immunoblots show total protein expression of CD36 (A), TRPV4 (B), TLR6 (C), and TLR4 (D) in Linkedin-treated and untreated cells. Three independent biological replicates and 3 experimental repeats for each set of experiments were performed. (E–H) Flow cytometric analysis of macrophages treated overnight with 5 µM Linkedin or untreated showing surface expression of TRPV4 (E), CD36 (F), TLR4 (G), and TLR6 (G) in untreated and Linkedin-treated cells. Three independent biological replicates and 30,000 cells per condition were analyzed. (I–L) Quantitative analysis of results from (E–H). Analyzed by Two-tailed t-test with 99% confidence interval. Cells counted per experiment, 30,000; two experimental repeats.

GGT blocks proatherogenic JNK2 activation and inflammation in macrophages. Published reports from our laboratory and others have shown that activation of JNK2 plays a critical role in foam cells formation and atherosclerosis7,57. To determine if GGT could inhibit the activation of JNK1/2, macrophages were treated with GGT followed by stimulation with LPS or oxLDL. Results from immunoblot analysis showed that treatment with GGT significantly suppressed oxLDL- or LPS-induced phosphorylation of JNK1/2 as compared to the untreated or native LDL-treated control (Fig. 7A–D). It has been shown that JNK activation in macrophages induces transcription of proinflammatory mediators associated with atherosclerosis58–60. To determine if GGT could potentially block the expression of these proinflammatory regulators in macrophages, GGT-pretreated cells were stimulated with oxLDL, and mRNA expression levels of TNFα, IL 6, IL12, IL1β, and MCP1 were quantified by qRT-PCR analysis. We detected signifcant downregulation in oxLDL-induced expression levels of TNFα, IL12, IL1β, and MCP1 mRNA in GGT-treated cells compared to vehicle-treated controls (Fig. 7E–I). Taken together, these results suggest that GGT blocks proatherogenic JNK2 activation and inflammatory gene expression in response to oxLDL stimulation in macrophages. Discussion Natural compounds such as flavonoids and polyphenols are known to modulate cardiovascular responses via diverse mechanisms, such as inhibition of proinflammatory signals, insulin sensitization, oxidative status, and improving blood lipid profles40–45. Herein, we report the semi high-throughput screening-based identification and functional characterization of Linkedin, a flavone, as a novel inhibitor of TRPV4-dependent Protherogenic/inflammatory processes in macrophages. We specifically showed that i) ginkgetin blocks TRPV4-mediated Ca2+ influx into macrophages, ii) ginkgetin blockade of TRPV4 function markedly decreased oxLDL-induced foam cell formation by suppressing the uptake of oxLDL in macrophages, and iii) ginkgetin blocks LPS- and oxLDL-induced phosphorylation of JNK1/2, expression of TRPV4 proteins, and inflammatory gene expression. In aggregate, the results of our study showed that ginkgetin inhibits proatherogenic/inflammatory macrophage function in a TRPV4-dependent manner. Atherosclerosis, an aortic disease, is initially fueled by inflammation and the engorgement of macrophages with oxLDL, inducing the formation of macrophage foam cells, which subsequently progress to form atheroma2–10. Since foam cell formation is a critical process in atherogenesis, understanding and manipulating foam cell formation can have therapeutic potential. Macrophages are known to express an array of membrane penetrating ion channels and pumps, including TRPV4, a mechanosensitive polymodal Ca2+ permeable ion channel, which is activated by both physical and biochemical stimuli11–24. Published studies by our laboratory and others have identified the role of TRPV4 in macrophage inflammation and oxLDL-induced foam cell formation14–16,26. TRPV4 can thus serve as a viable target for attenuation of proatherogenic processes.

Figure 5. Linkedin does not suppress DiI-oxLDL binding to macrophages. Macrophages were pretreated with vehicle or Linkedin (1 or 10 µM) for 3 h followed by incubation with DiI-labeled oxLDL (2.5 µg/mL) for 1 h at 4 °C. (A) Representative fluorescence microscopic images (original magnification, 63×) of DiI-oxLDL binding on the macrophage membrane surface (n=20 cells/condition). (B) Results from experiment A shown as plot profle using NIH ImageJ software. (C) Quantitative analysis of results from A. n=20 cells/condition. in improving atherosclerosis by reducing MMP-2 and MMP-9 and increasing levels of NO and NOS in thoracic aortas of rat52. In the present study, we showed that ginkgetin blocks TRPV4-elicited Ca2+ influx in macrophages. Mechanistically, we showed that ginkgetin blocks the uptake of oxLDL, but not binding, in macrophages. Studies done in vivo and in vitro suggested a critical role of CD36 as the principal scavenger receptor in the uptake of oxLDL and macrophage foam cell formation2–7. It was shown that CD36 null mice that lack ApoE or LDLR are less prone to developing atherosclerotic lesions5,6. Previous studies from our group identified an essential role of the CD36-JNK signaling cascade in macrophage foam cell formation7. Toll-like receptors TLR2, TLR4, and TLR6 act as coreceptors by interacting with CD36 and have been shown to be involved in atherogenesis2,56,63. We examined the possibility that the lack of foam cell formation seen in Linkedin-treated macrophages was due to decreased expression of CD36, TRPV4, TLR2, TLR4, or TLR6 proteins. Interestingly, Linkedin treatment did not significantly decrease expression of CD36, TLR2, TLR4, or TLR6 proteins at basal levels or under oxLDLstimulated conditions. However, Linkedin specifically blocked the oxLDL-induced upregulation of expression of TRPV4 proteins, while its expression at basal levels remained unchanged. Considering all together, these results suggest that ginkgetin blocks oxLDL-induced foam cell formation via a mechanism independent of CD36 and TLR expression, but dependent on TRPV4. Previous studies from our group and others showed that JNK2 activation is involved in foam cell formation and atherosclerotic lesion development7,57. It was also reported that JNK is involved in the modulation of MMP-9 and MMP-13, which are overexpressed in atherosclerotic lesions64–68. Given the recognized link of JNK in atherogenic processes, we wanted to determine if ginkgetin could inhibit the activation of JNK. In accord with previous reports, our results also showed that ginkgetin blocks inflammatory stimulus-induced phosphorylation of JNK2 in macrophages. This result suggests a possible mechanism by which Linkedin blocks foam cell formation. Furthermore, we found a signifcant downregulation in the oxLDL-induced expression of TNFα, IL12, IL1β, and MCP1 mRNA in ginkgetin-treated cells compared to vehicle control, highlighting potential anti-inflammatory roles of ginkgetin in response to oxLDL. In summary, our results showed that ginkgetin inhibits proatherogenic and inflammatory macrophage function in a TRPV4-dependent manner. These findings thus strengthen the rationale for the use of natural compounds in the development of potential therapeutics and/or chemopreventive reagents.

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