Figures
Abstract
Vitamin D is a known modulator of inflammation. Native dietary vitamin D3 is thought to be bio-inactive, and beneficial vitamin D3 effects are thought to be largely mediated by the metabolite 1,25(OH)2D3. Reduced serum levels of the most commonly measured precursor metabolite, 25(OH)D3, is linked to an increased risk of multiple inflammatory diseases, including: cardiovascular disease, arthritis, multiple sclerosis, and sepsis. Common to all of these diseases is the disruption of endothelial stability and an enhancement of vascular leak. We previously performed an unbiased chemical suppressor screen on a genetic model of vascular instability, and identified cholecalciferol (D3, dietary Vitamin D3) as a factor that had profound and immediate stabilizing and therapeutic effects in that model. In this manuscript we show that the presumed inactive sterol, D3, is actually a potent and general mediator of endothelial stability at physiologically relevant concentrations. We further demonstrate that this phenomenon is apparent in vitamin D3 metabolites 25(OH)D3 and 1,25(OH)2D3, and that the effects are independent of the canonical transcription-mediated vitamin D pathway. Our data suggests the presence of an alternative signaling modality by which D3 acts directly on endothelial cells to prevent vascular leak. The finding that D3 and its metabolites modulate endothelial stability may help explain the clinical correlations between low serum vitamin D levels and the many human diseases with well-described vascular dysfunction phenotypes.
Citation: Gibson CC, Davis CT, Zhu W, Bowman-Kirigin JA, Walker AE, Tai Z, et al. (2015) Dietary Vitamin D and Its Metabolites Non-Genomically Stabilize the Endothelium. PLoS ONE 10(10): e0140370. https://doi.org/10.1371/journal.pone.0140370
Editor: Andrzej T. Slominski, University of Alabama at Birmingham, UNITED STATES
Received: July 21, 2015; Accepted: September 24, 2015; Published: October 15, 2015
Copyright: © 2015 Gibson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by NIH Grants 1R01NS080893-01A1 (PI: Li, Dean Y.), 2R01HL077671-09 (PI: Li, Dean Y.), and 2R01HL-084516-05A1 (PI: Li, Dean Y.), and Veteran's Affairs Merit Award 1IOBX002976 (PI: Li, Dean Y.) The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Recursion Pharmaceuticals, LLC provided support in the form of salaries for authors CCG, CTD, KRT and DYL, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the 'author contributions' section.
Competing interests: The authors have the following interests. The University of Utah has licensed 'know how' related to this manuscript to Recursion Pharmaceuticals, a biotechnology company owned in part by the University of Utah Research Foundation. Christopher C. Gibson and Dean Y. Li are co-founders of Recursion Pharmaceuticals, while Chadwick T. Davis and Kirk R. Thomas are employed by Recursion Pharmaceuticals. Christopher C. Gibson, Chadwick T. Davis, Kirk R. Thomas and Dean Y. Li have real or optional ownership interest in Recursion. There are no further patents, products in development or marketed products to declare. This does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.
Introduction
There exists an inverse correlation between measured vitamin D levels and the pathology or incidence of the leading causes of death: cardiovascular disease, stroke, chronic obstructive pulmonary disease (COPD), infection, and cancer [1–9]. Vitamin D deficiency is also linked to multiple autoimmune diseases including multiple sclerosis, arthritis, lupus, and type-1 diabetes [10–15]. Although the classical role of Vitamin D is to maintain calcium homeostasis and promote bone health, more recent studies have shown that Vitamin D, acting through immune cells, induces an anti-inflammatory response, providing a plausible link to many of the aforementioned diseases [16].
A hallmark of inflammation is the activation and destabilization of the endothelial cells lining the vasculature, leading to dysfunctional nutrient exchange, inflammatory cell migration, and dysregulated activation of the clotting cascade [17, 18]. Endothelial destabilization and activation occurs as a result of injury, altered hemodynamics, response to cytokines or other inflammatory cues, as well as genetic diseases [19, 20]. Therapies designed to stabilize the vascular endothelium have been shown to limit the pathology from a diverse array of inflammatory diseases including infection, arthritis, cancer, retinopathy and more [21–25]. Our studies to identify chemical suppressors of the phenotype of one such genetic disease, cerebral cavernous malformation (CCM), identified vitamin D3 (D3, cholecalciferol, calciol, ‘dietary vitamin D3’) as a factor that rescued the destabilized vasculature of CCM in vitro and in vivo [26].
D3 is ingested in foods such as fish, and is also synthesized endogenously by the action of ultraviolet light on 7-dehydrocholesterol (7-DHC) in the skin14. D3 is hydroxylated to 25-hydroxy vitamin D3 (25(OH)D3, calcidiol, ‘prohormonal vitamin D3’) in the liver by CYP2R1 [27]. 25(OH)D3 is further hydroxylated to 1α,25-dihydroxy vitamin D3 (1,25(OH)2D3, calcitriol, ‘hormonal vitamin D3’) by CYP27B1 in the kidney [28]. Both D3 and 25(OH)D3 are widely considered to be biologically inactive, serving only as precursor metabolites of the active form 1,25(OH)2D3. 1,25(OH)2D3, a hormone vital to calcium homeostasis and the immune response, acts through the well-characterized nuclear hormone receptor Vitamin D Receptor (VDR) [29]. Having observed endothelial stabilizing activity of D3 in CCM2 deficient cells, we wanted to determine if D3 and its metabolites are able to serve as general modulators of endothelial stability.
Herein, we show that the previously assumed inactive sterol, vitamin D3, is a potent and general mediator of endothelial stability at physiologically relevant levels. We observe this stabilizing effect with D3 and the metabolites 25(OH)D3 and 1,25(OH)2D3), but not the vitamin D precursor 7-dehydroxy cholesterol (7-DHC). We also show that the stabilizing effect is broad as it inhibits permeability induced by diverse pro-inflammatory cues. Finally, we determine that this effect is non-genomic, and that it occurs in conjunction with the deactivation of ARF6, RhoA, and the stabilization of VE-Cadherin at the plasma membrane.
The prevalent hypothesis to explain the inverse correlation between vitamin D status and diverse diseases is that 1,25(OH)2D3 acts directly on immune cells through the vitamin D receptor (VDR) to modulate the immune response [30]. Our data identify an additional role for vitamin D in which the vitamin D sterols act directly on the endothelium to stabilize barrier structure and function, thereby reducing vascular leak into the surrounding tissues. This new observation may explain, in part, the broad associations between vitamin D and many diseases.
Materials and Methods
Ethics Statement
All mouse experiments were approved by the University of Utah Institutional Animal Care and Use Committee and the George E. Wahlen Department of Veterans Affairs Medical Center Institutional Animal Care and Use Committee.
Cells and Culture Conditions
Primary dermal human microvascular endothelial cells (HMVEC-D) were purchased from Lonza at passage 0 (p0), grown in EGM2-MV (Lonza) and experiments were performed from p4-p7 in EBM2 supplemented with 0.1% BSA.
Trans-endothelial resistance (TEER)
The ECIS system was used with 8-well plates (8W10E+, Applied Biophysics), with cells seeded at 2.5x104 cells/well. Transcription and translation inhibition experiments were performed using a Roche SP Xcelligence transendothelial system and 96-well assay plates with cells seeded at 1x104 cell/well. Treatment in all assays, unless otherwise denoted were 10μm D3 (Tocris), 7-DHC (Sigma) or vehicle (0.5% DMSO) and simultaneous cytokine addition of either TNF-α (2ng/mL) or IL-1β (10ng/mL).
Transwell permeability
HMVEC-D cells were seeded on 1.0μm BD FalconTM Cell-Culture Inserts coated with human fibronectin. Cells were grown to confluence and pre-treated with 10μm D3 (Tocris), 7-DHC (Sigma) or vehicle (0.5% DMSO) on both apical and basolateral sides of the monolayer for 30 minutes. Cytokines, TNF-α (2ng/mL) or IL-1β (10ng/mL), were then added to both the apical and basolateral sides of the monolayer. Four hours following cytokine addition, a FITC-dextran (40kDa) reporter was added to each upper chamber, reaching a final concentration of 1mg/mL. The solutions were removed from each bottom chamber 60 minutes following FITC-dextran addition. The concentrations of FITC-dextran in the lower chamber solutions were measured using fluorimetry (excitation wavelength = 485nm; emission measured at 530nm) and concentrations were calculated via standard curve. Data are presented as a mean ± SEM of three independent experiments, with four replicates per condition in each experiment.
Ex-vivo cerebral artery permeability
Mice were euthanized by exsanguination via cardiac puncture while under isoflurane anesthesia. The brain was excised and placed in a cold physiological salt (pH 7.4 @ 4 C) and ~100 μm diameter middle cerebral arteries were dissected and placed in a pressure myograph (DMT Inc) containing physiological salt solution (PSS, 145.0 mM NaCl, 4.7 mM KCl, 2.0 mM CaCl2, 1.17 mM MgSO4, 1.2 mM NaH2PO4, 5.0 mM glucose, 2.0 mM pyruvate, 0.02 mM EDTA, 3.0 mM MOPS buffer and 1 g/100 ml BSA, pH 7.4. Arteries were cannulated onto glass micropipettes, secured with nylon (11–0) suture and perfused with PSS. Once cannulated, the middle cerebral arteries were checked for leaks, warmed to 37C, pressurized to 70 mmHg and allowed to equilibrate for ~1 hour. 70 kD FITC labeled dextran (.14 mg/ml) in PSS was infused intraluminally. Vessels that leaked upon initial inspection were excluded. The artery was protected from the light and 100 μl samples were collected from the bath surrounding the cannulated artery at 0, 1, 2, 2.5 and 3 hours after VEGF treatment (2.5 X 10-5mg/ml). FITC fluorescence measures were made in collected PSS via a Synergy 4 plate reader (BioTek) and are expressed in relative fluorescent units (RFU) and normalized to the RFU for the physiological saline.
Western blot and Phosphorylation assays
Human dermal microvascular endothelial cells (HMVEC-D) were grown to confluence and starved in Endothelial Cell Basal medium-2 (EBM-2) + 0.1% BSA for 4 hours. Then the cells were stimulated with 10ng/ml IL-1β with 10μm D3 (Tocris), 7-DHC (Sigma) or vehicle (0.5% DMSO) for 10 min, or 2ng/ml TNFα with 10μm D3 (Tocris), 7-DHC (Sigma) or vehicle (0.5% DMSO) for 15 min. After treatment, the cells were washed with ice-cold PBS and lysed in 50mM Tris pH 7.4, 150mM NaCl, 10mM MgCl2, 10% Glycerol, 1% NP-40, with protease and phosphatase inhibitors (Roche). Lysates were combined with 2X sample buffer, separated by SDS-PAGE and probed with antibodies to phospho-VE-cadehrin Y731 (Invitrogen), phospho-Src Y418 (Cell signaling), VE- cadherin (Cell signaling), Src (Cell signaling), FoxO1 (Cell signaling) and CYP24 (Thermo) at 1:1000. For RhoA, ARF6, Rac1 /cdc42 and R-Ras activation assays, crude total cell lysate were generated and GTP-RhoA, ARF6, Rac1/ cdc42 and R-Ras were precipitated with Rhotekin-RBD (Millipore), GGA3-PBD (Cell Biolabs), PAK-1-PBD (Millipore) and Raf-1 RBD respectively. Following three washes with lysis buffer, bound proteins were eluted with 2X sample buffer. RhoA, ARF6, Rac1 /cdc42 and R-Ras was detected by western blotting with antibodies (RhoA, Rac1 and R-Ras antibody are from Cell Signaling, ARF6 and cdc42 antibody are from Millipore). Each blot is representative of at least three independent experiments, for which densitometry is shown.
VE-Cadherin area quantification
10,000 HMVEC per well were seeded on BD-Falcon clear-bottom 96-well tissue culture plates (catalog number 353219) and allowed to grow for 48–72 hours. Cells were treated with denoted molecules for 24 hrs and then fixed with 4% paraformaldehyde in PBS for 10 min. Plates were then blocked with Odyssey™ Blocking Buffer (Licor Biosciences) for 30 min at room temperature, and then a mouse monoclonal VE-Cadherin antibody (Cell Signaling clone D87F2, Cat #2500) over night at 4°C. Cells were rinsed 3X with PBS and incubated with Alexa Fluor® 488 donkey anti-mouse secondary and Hoechst 33258 dye for 4 hr at room temperature. Cells were rinsed and the Molecular Devices ImageXpress Micro XLS collected images at the center of each well with a 20X objective. VE-cadherin area of each image was quantified with ImageJ by batch thresholding all images from an individual experiment and quantifying the number of pixels that were VE-Cadherin positive within each image. Data are compiled from three independent experiments with at least three replicate wells per condition in each experiment.
Results
D3 and its metabolites stabilize vascular endothelial cells
Although vitamin D levels are known to correlate with a variety of indicators of health, this relationship is thought to be mediated through the direct action of 1,25(OH)2D3 in inflammatory cells [10, 30]. However, we previously found that dietary vitamin D3 directly alleviated stability defects in a cellular model of CCM disease [26]. However, because D3 is presumed to be biologically inactive, we sought to characterize the stabilizing effects of all three basic forms of vitamin D (D3, 25(OH)D3, and 1,25(OH)2D3) in primary human microvascular endothelial cells. Electric cell-substrate impedance sensing (ECIS), an indirect measure of monolayer integrity, was used initially to characterize the stability of endothelial monolayers in the presence of various Vitamin D3 related compounds. When administered to the apical side of endothelial monolayers, all three forms of vitamin D3 increased baseline endothelial stability within minutes (Fig 1A–1O). We also observed statistically significant activity for all three metabolites at doses as low as 100pM, commensurate with documented circulating levels of 25(OH)D3 and D3 [31]. Surprisingly, the purportedly inactive dietary form, D3, was the most potent of the three sterols across the range of doses from 100 pM to 10 μM.
Dose/time resistance (endothelial stability) surfaces generated with ECIS are shown from 100 pM to 10 μM and from zero to 21 hours for: (A) D3; (F) 25(OH)D3; (K) 1,25(OH)2D3. Detailed time-responses are shown at 1 nM and 10 μM respectively for: (B and C) D3; (G and H) 25(OH)D3; and (L and M) 1,25(OH)2D3. Detailed dose-response are shown at 4 hours and 12 hours respectively for (D and E) D3, (I and J) 25(OH)D3, and (N and O) 1,25(OH)2D3.
Given the basal modulatory effects on the endothelium, we next asked if D3 could exhibit protective effects in the face of pro-inflammatory cues. We challenged endothelial monolayers in vitro in the presence of D3 with the inflammatory signals, interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), or bacterial lipopolysaccharides (LPS) (Fig 2A–2C). ECIS demonstrated that D3, but not its precursor 7-dehydrocholesterol (7-DHC), inhibited the destabilizing effects of all of these diverse signals. Because the ECIS readout may also reflect changes in cell shape and cell-substrate adhesion, we confirmed this observation in a transwell assay, a direct measure of monolayer leak, and observed less flux of a 40kD FITC dextran reporter from the apical to basolateral side across endothelial monolayers (Fig 2D). Finally, to determine whether the broad stabilizing effects of D3 on the endothelium translated to an animal model, we examined cerebrovascular leak in wild-type mice fed either standard chow (1.5 IU/g D3) or an identical chow enhanced with D3 (25 IU/g). We found that cerebral arterioles isolated from mice fed a diet high in D3 had significantly less VEGF-induced leak of a fluorescent reporter from the lumen through the vessel wall compared to mice fed a standard diet (Fig 2E). These data suggest that the vitamin D sterols act directly on the endothelium to suppress the destabilizing actions of diverse environmental stimuli.
Monolayers of HMVEC were stimulated with D3 (10 μM), 7-DHC(10 μM), or 0.5% DMSO (vehicle control) in the presence of inflammatory cytokines: IL-1β (10 ng/mL), TNF-α (2 ng/mL), and LPS (100 ng/mL) in an (A-C) ECIS or (D) transwell leak assay. (E) VEGF-induced leak of a fluorescent reporter in arterioles isolated from wild-type mice fed either standard chow or a D3-enhanced chow. All panels depict mean ± SEM. * denotes P<0.05, ** denotes P<0.01, and **** denotes P<0.0001.
D3 blocks RhoA and ARF6 activation in endothelial cells
To determine the mechanism of D3’s activity in endothelial cells, we assessed the activation of markers within the key signaling pathways involved in endothelial stability: transforming protein RhoA (RHOA), Ras-related C3 botulinum toxin substrate 1 (RAC1), cell division control protein 42 homolog (CDC42), ADP-ribosylation factor 6 (ARF6), proto-oncogene tyrosine-protein kinase Src (SRC), or Ras-related protein R-Ras (RRAS) [21, 22, 32–35]. Treatment of HMVEC with D3 suppresses both TNF-α or IL-1β activation of RHOA and ARF6 (Fig 3A–3D and S1 Fig). D3 did not modulate the baseline activation of markers left unaltered by TNF-α or IL-1β (Fig 3E–3l and S1 Fig). Taken together, these data suggest that D3 can rapidly affect a subset of key intracellular signaling pathways that play a role in endothelial activation in the context of cytokine-induced destabilization.
Endothelial cells were exposed to 10 μM D3 or 7-DHC in combination with 2ng/mL TNF-α or IL-1β. Lysates were analyzed for RHOA-GTP and ARF6-GTP levels using appropriate precipitation assays. All graphs depict mean ± SEM. * denotes P<0.05, ** denotes P<0.01, and *** denotes P<0.001.
D3 stabilizes junctional VE-cadherin
Activated ARF6 (ARF6-GTP) has been shown to play a key role in the destabilization of vascular endothelial cadherin (VE-Cadherin) cell-cell junction proteins, resulting in endothelial monolayer disruption [21, 22]. This activity of ARF6 is mediated through the phosphorylation of tyrosine 731 (pY731) on VE-Cadherin, which destabilizes cadherin-cadherin interaction and leads to VE-Cadherin internalization [36, 37]. Not only did D3 inhibit the TNF-α-induced phosphorylation of VE-cadherin, (Fig 4A and S2 Fig), it strengthened the integrity of cell-cell junctions, measured immunocytochemically by VE-Cadherin quantification, between cells exposed to IL-1β and TNF-α (Fig 4B). Collectively, these data suggest that D3 may inhibit the destabilizing effects of cytokines on cell-cell junctions through a common node.
(A) Endothelial cells were treated with TNF-α and either 7-DHC or D3 for the denoted times and lysates were immunoblotted for p731 VE-cadherin or total VE-Cadherin. (B) Endothelial cell monolayers were exposed to the denoted pro-inflammatory cues in the presence of vehicle control, D3 or 7DHC. Cells were fixed and VE-Cadherin was visualized through immunofluorescent labeling with automated image acquisition and analysis. All graphs depict mean ± SEM. * denotes P<0.05, ** denotes P<0.01, and *** denotes P<0.001.
D3 acts on endothelial cells through a non-genomic mechanism
1,25(OH)2D3 is the high-affinity ligand for the nuclear hormone receptor VDR [29, 38–41]. VDR is a transcription factor, though it can also act rapidly via non-transcriptional mechanisms to modulate calcium influx and activate protein kinase c [29, 38, 39, 42]. D3 is not considered to be a ligand of VDR, except at non-physiologic doses, and fails to activate known VDR-dependent pathways [29, 39, 41]. 25(OH)D3 is also generally considered not to be a high-affinity ligand of VDR, however, in some reports it has been observed to be an agonist of the receptor [29, 38, 39, 41, 43]. Given the considerable evidence suggesting the biologic inactivity of D3 and 25(OH)D3 in the endothelium, we wondered whether the stabilizing effects of these purportedly inactive compounds could be explained by endothelial-mediated conversion to 1,25(OH)2D3. To determine whether D3 was being converted into 1,25(OH)2D3, we measured the ability of D3 and 25(OH)D3 to enhance expression of CYP24A1, a gene that has been reported to be highly expressed as result of 1,25(OH)2D3 induced VDR activation [44, 45]. Despite the rapid (within minutes) effects of D3 in our previous assays, treatment of HMVEC with D3 for 24 hours had no measurable effect on expression of VDR target CYP24A1, suggesting D3 was not converted to 1,25(OH)2D3 (Fig 5A). Confirming the validity of the assay, treatment with 1,25(OH)2D3 led to a significant increase in CYP24A1 expression after a 24 hour treatment. 25(OH)D3 induced an increase in CYP24A1, consistent with reports of endothelial conversion of 25(OH)D3 to 1,25(OH)2D3, but not of conversion of D3 to 1,25(OH)2D3 [46]. The observation that all three of the vitamin D sterols exhibit a stabilizing effect, but only two induce the expression of VDR target genes, suggests that the sterols stabilize the endothelium in a manner indpendent from canonical, genomic vitamin D receptor signaling.
(A) Endothelial cells were exposed to D3 or its metabolites for 24 hours and lysates were probed for VDR transcription targets FOX01 and CYP24. Endothelial cells were exposed to D3 or its metabolites in the presence of inhibitors of transcription (actinomycin D) and translation (cycloheximide) (B, C) and were assessed for transendothelial resistance or VDR target gene expression. All graphs depict mean ± SEM. * denotes P<0.05, and **** denotes P<0.0001. ### denotes P<0.001, and #### denotes P<0.0001 versus the respective control.
1,25(OH)2D3 is reported to have both genomic and non-genomic activities in multiple tissue and cell types [38, 39]. To test if the effects of D3 were genomic and dependent upon de novo gene expression, we examined the effect of D3 on trans-endothelial resistance in the presence of transcription and translation inhibitors (actinomycin-D and cycloheximide, respectively), and found that while these inhibitors blocked the production of the VDR-target CYP24, they had no effect on the stabilizing effect of D3 on the endothelium (Fig 5B and 5C). These data suggest D3 has an immediate and direct stabilizing effect on the endothelium, which is not the result of conversion to 1,25(OH)2D3, transcription, or translation.
Discussion
Our data show that vitamin D3 and its metabolites, 25(OH)D3, and 1,25(OH)2D3, can modulate endothelial stability even in the face of diverse inflammatory cues such as cytokines and lipopolysaccharides. This stabilizing effect, combined with our prior observation that D3 preserves vascular integrity in cells deficient in CCM2, suggests there may exist a novel function for vitamin D3 in homeostasis by directly maintaining or enhancing the barrier function of the endothelium. Importantly, we also show that the barrier-enhancing function of vitamin D3 is not limited to what is commonly referred to as the “active metabolite” 1,25(OH)2D3, but this activity is present in the “inactive” dietary and mono-hydroxylated forms of the vitamin as well.
Vitamin D has received much attention over the last decade due to the inverse correlation between serum levels of 25(OH)D3 and the leading causes of death: cardiovascular disease, stroke, COPD, infection, cancer, as well a number of autoimmune diseases [29, 47]. Vascular instability is a hallmark of such inflammatory diseases, and we and others have previously demonstrated that prevention of vascular destabilization reduces pathology in inflammatory diseases arthritis and septic shock [21–23, 48–50]. In many of the reports characterizing a relationship between 25(OH)D3 and disease, D3 concentration is ignored and investigators have presumed that 25(OH)D3 is not itself active in these disease states [29, 47]. Instead, the assumption has typically been that serum 1,25(OH)2D3 levels mirror serum 25(OH)D3, or that 25(OH)D3 is locally converted to 1,25(OH)2D3 in tissues implicated in disease progression [28, 29, 47]. In many cases, however, these assumptions go untested, and such a mechanism may not be entirely responsible for the beneficial effects of vitamin D.
We have thus far described a novel function for vitamin D and its metabolites by which they are similarly bioactive and promote immediate, direct, and stabilizing effects on the endothelium that counter the disruptive effects of inflammatory cues (Fig 6). All three vitamin D metabolites tested in our assays have similar potency in mediating endothelial stability. In humans, circulating serum levels of D3 and 25(OH)D3 are present in the nanomolar range, approximately 1,000 fold higher than 1,25(OH)2D3[28]. These data raise the possibility that the traditionally ‘inactive’ metabolites D3 and 25(OH)D3 might play more prominent roles in controlling endothelial stability and disease compared to 1,25(OH)2D3, which is not reported to circulate at levels necessary for the observed stabilizing phenomena. Additionally, because the ‘inactive’ sterols can promote stabilizing activity at doses lower than necessary for an interaction with VDR, the stabilizing phenomena may occur in a VDR-independent manner. While this study does not call into question a role for 1,25(OH)2D3 or VDR in immunomodulatory mechanisms, our results illuminate an alternative pathway of vitamin D activity, and raise the interesting possibility that inverse correlations between serum 25(OH)D3 levels and certain diseases could be due to the direct effects of D3 and 25(OH)D3 on endothelial stability.
Graphical models of the different vitamin D3 sterols, their metabolism, and a summary of their normal circulating levels, the minimum active dose for stabilizing the endothelium and doses in which the sterols have been reported to interact with vitamin D receptor [29, 51, 52]. *Normal circulating levels vary upon many conditions including diet and UV exposure.
Supporting Information
S1 Fig. D3 blocks RHOA and ARF6 activation in destabilized endothelial cells (western blot replicates).
Endothelial cells were exposed to 10 μM D3 or 7-DHC in combination with 2ng/mL TNF-α or IL-1β. Lysates were analyzed for RHOA-GTP and ARF6-GTP levels using appropriate precipitation assays.
https://doi.org/10.1371/journal.pone.0140370.s001
(TIF)
S2 Fig. D3 promotes VE-cadherin cell-cell junction stability (western blot replicates).
Endothelial cells were treated with TNF-α and either 7-DHC or D3 for the denoted times and lysates were immunoblotted for p731 VE-cadherin or total VE-Cadherin.
https://doi.org/10.1371/journal.pone.0140370.s002
(TIF)
Acknowledgments
We thank, D. Lim for graphical assistance; J. Phillips, B. Luo, and C. Rodesch at The University of Utah Cell Imaging/Fluorescence Facility and Drug Discovery Core Facility; A. Schlegel, J. Rutter, S. Odelberg, K. Ostanin, and A. Mueller for critical comments and helpful scientific discussions.
Author Contributions
Conceived and designed the experiments: CCG CTD KRT LAL AJD DYL. Performed the experiments: CCG CTD WZ JAB-K AEW ZT. Analyzed the data: CCG CTD WZ JAB-K AEW. Contributed reagents/materials/analysis tools: DYL LAL AJD. Wrote the paper: CCG CTD KRT DYL.
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