Cyclosporin A differentially inhibits multiple steps in VEGF induced angiogenesis in human microvascular endothelial cells through altered intracellular signaling
© Rafiee et al; licensee BioMed Central Ltd. 2004
Received: 12 January 2004
Accepted: 02 June 2004
Published: 02 June 2004
The immunosuppressive agent cyclosporin A (CsA), a calcineurin inhibitor which blocks T cell activation has provided the pharmacologic foundation for organ transplantation. CsA exerts additional effects on non-immune cell populations and may adversely effect microvascular endothelial cells, contributing to chronic rejection, a long-term clinical complication and significant cause of mortality in solid-organ transplants, including patients with small bowel allografts. Growth of new blood vessels, or angiogenesis, is a critical homeostatic mechanism in organs and tissues, and regulates vascular populations in response to physiologic requirements. We hypothesized that CsA would inhibit the angiogenic capacity of human gut microvessels. Primary cultures of human intestinal microvascular endothelial cells (HIMEC) were used to evaluate CsA's effect on four in vitro measures of angiogenesis, including endothelial stress fiber assembly, migration, proliferation and tube formation, in response to the endothelial growth factor VEGF. We characterized the effect of CsA on intracellular signaling mechanisms following VEGF stimulation. CsA affected all VEGF induced angiogenic events assessed in HIMEC. CsA differentially inhibited signaling pathways which mediated distinct steps of the angiogenic process. CsA blocked VEGF induced nuclear translocation of the transcription factor NFAT, activation of p44/42 MAPK, and partially inhibited JNK and p38 MAPK. CsA differentially affected signaling cascades in a dose dependent fashion and completely blocked expression of COX-2, which was integrally linked to HIMEC angiogenesis. These data suggest that CsA inhibits the ability of microvascular endothelial cells to undergo angiogenesis, impairing vascular homeostatic mechanisms and contributing to the vasculopathy associated with chronic rejection.
The calcineurin inhibitor cyclosporin A (CsA) is a potent immunosuppressive agent that has formed the pharmacologic cornerstone of solid organ transplantation. CsA prevents the activation of lymphokine genes essential for T cell proliferation by disrupting calcium-dependent signal transduction pathways in leukocytes . Although pharmacologic studies of CsA have focused primarily on T cell responses, there is emerging evidence that this agent may exert potent effects on blood vessels, promoting arterial hypertension, inducing long-term vascular dysfunction, and contributing to obliterative vasculopathy in chronic transplant rejection [2–5]. At the present time, chronic rejection with its associated vasculopathy, is the major cause of late allograft dysfunction, including patients with intestinal transplants [6, 7].
In solid-organ transplantation, the vascular endothelium has received attention because of its unique role as the interface between the donor graft and the host's circulating immune cells, and as a focus of acute rejection [8, 9]. More recent investigation has demonstrated that the endothelium plays a central role in chronic rejection, where inappropriate activation of endothelial cells results in obliterative vasculopathy and accelerated post-transplant atherosclerosis , a major cause of morbidity and mortality in solid organ transplant recipients. Activation of graft endothelium in chronic rejection may result from host/graft immunologic attack, as well as dysfunction associated with transplant immunosuppression . In transplantation of the small bowel, microvascular dysfunction may contribute to more significant problems with both acute and chronic rejection in these patients. Indeed, small bowel transplantation has been one of the more problematic clinical areas in the realm of solid organ grafts, where patients require increased immunosuppressive regimens and have had overall, less successful clinical outcomes [11–13].
The growth of new microvessels, or angiogenesis, is now appreciated to be a critical biologic process involved in tissue homeostasis. Angiogenesis is initiated by local activation of genes encoding diffusable angiogenic factors, or by the release of vascular growth factors which subsequently act on local microvasular cell populations, as well as by a decrease in local angiostatic factors, including interferon beta . Angiogenesis involves an orchestrated sequence of steps which include endothelial activation, stress fiber assembly, fibrinolysis, proteolytic degradation of the basement membrane and the extracellular matrix, migration, proliferation and neovascularization . One of the major angiogenic growth factors is the vascular endothelial growth factor (VEGF), which selectively induces activation, migration, proliferation and tube formation in endothelial cells in vitro. VEGF is a 34–42 kDa glycoprotein which exerts its biological effects on endothelial cells through its two major tyrosine kinase receptors, VEGFR1/Flt-1 (fetal liver kinase-1) and VEGFR2/Flk-1/KDR (kinase insert domain containing receptor). By binding to these receptors, VEGF activates various signaling cascades, including the mitogen activated protein kinase family (ERK1/2, p38 MAPK and SAPK/JNK) and phosphoinositol3-kinase (PI3 kinase) [16, 17]. A downstream result of these signaling events is the expression of COX-2, which plays an integral role in VEGF induced angiogenesis [18–20]. Finally, investigation has demonstrated a pivotal role for the transcription factor nuclear factor activated in T-cells (NFAT) in the angiogenic signaling of VEGF in human umbilical vein endothelial cells (HUVEC) , which is inhibited by CsA. Thus, there is a potential role for CsA in blocking angiogenesis in microvascular cell populations, potentially through its effect on NFAT.
An integrated analysis of the effect of CsA on the multiple stages of the angiogenic process in human organ specific microvascular endothelial cells has not been performed to date. Studies evaluating the effect of CsA on human umbilical vein endothelial cells  may not accurately reflect microvascular events, and are further complicated by their wide functional variability in tissue culture, causing discrepant results reported by different laboratories . In addition, it is also now appreciated that human microvascular endothelial cells derived from differentiated, organ specific vascular beds have been shown to differ significantly from HUVEC in their responsiveness to cytokines, the expression profile of antigens, and the elaboration of secretory products [24–27]. We investigated the mechanisms of VEGF-induced endothelial cell signaling and angiogenesis in HIMEC, an organ specific microvascular cell population, and the effect of CsA on four in vitro components of angiogenesis, including stress fiber assembly, migration, proliferation/growth and tube formation.
VEGF, but not TNF-α/LPS, enhances growth of HIMEC
Effect of CsA on VEGF induced stress fiber assembly in HIMEC
Immunosuppressive agents inhibit VEGF induced migration, proliferation and growth of HIMEC
Matrigel™ In vitro-Tube Formation in HIMEC
VEGF enhances phosphorylation of MAPK
Effect of VEGF on Nuclear Factor of Activated T cells (NFAT) in HIMEC
DNA-binding activity of NFATp, NF-κB and AP-1 in VEGF activated HIMEC
VEGF increases COX-2 gene expression in HIMEC
In this study, we demonstrate that CsA exerts potent effects on the angiogenic capacity of human microvascular endothelial cells, differentially inhibiting multiple stages in the in vitro angiogenic process. This inhibitory effect of CsA on VEGF function in HIMEC involved 1) actin assembly and stress fiber formation, 2) cell migration, 3) proliferation and monolayer expansion (growth), and 4) tube formation. Furthermore, experiments focusing on the effect of CsA on signaling events following VEGF induced HIMEC activation demonstrated blockade of the DNA binding activity of the transcription factor NFAT, complete inhibition of p44/42 MAPK activation, partial inhibition of p38 MAPK, and complete inhibition of COX-2, with no effect on AP-1 activation. Furthermore, our data demonstrate that these signaling cascades play specific roles in the four components of angiogenesis which were modeled in our human organ specific microvascular system, and were differentially affected by CsA. Thus, CsA effects multiple signaling pathways in VEGF induced angiogenesis, which may ultimately impact on vessel growth, an important component of vascular homeostasis and may contribute to the vasculopathy of chronic rejection.
Receptor tyrosine kinases and their ligands play a crucial role in vascular development, and considerable progress has been made toward understanding the cellular and molecular events in angiogenesis . Activation of endothelial signal transduction pathways are essential aspects of neovascularization, as endothelial activation must occur for cells to undergo angiogenesis. Although the biological functions of VEGF and its role in the angiogenic process have been extensively explored, the intracellular signaling pathways that lead to distinct gene expression patterns and altered endothelial physiology in response to VEGF in human organ specific microvascular endothelial cell populations remain incompletely defined, nor has the VEGF induced signaling in endothelial cells been characterized in an integrated fashion. Data obtained in this study demonstrate that VEGF activation of HIMEC results in activation all three MAPK members (ERK1/2, p38 MAPK and SAPK/JNK) and resulted in increased both migration and proliferation. Signaling through MAPKs are heavily dependent on the immediate environment which surrounds the endothelial cell. ERK1/2 is generally involved with cell growth and proliferation, whereas SAPKs are usually known to transduce stress signals . Here we have shown that biological effects of VEGF on endothelial cells are concentration dependent, as 10 ng/ml VEGF resulted in HIMEC migration, p38 MAPK activation and actin/stress fiber formation while higher concentrations (i.e. 50 ng/ml) resulted in activation of p44/42 MAPK, COX-2 expression, NFAT activation and increased cell proliferation. This is in agreement with Rousseau et al.  and Seetharam et al. , who have shown that exposure of human umbilical vein endothelial cells (HUVEC) to concentrations of VEGF that increase cell migration also promotes actin polymerization, formation of stress fibers and recruitment of vinculin to ventral plaques. Actin fibers disappeared in HIMEC exposed to higher concentrations of VEGF (50–100 ng/ml) and cell migration was also diminished. SB203580, a p38 MAPK specific inhibitor blocked both cell migration and actin polymerization without affecting cell proliferation. Thus, our data suggest that p38 MAPK activation by VEGF plays a critical role in HIMEC migration by regulating actin polymerization dynamics and organization. Interestingly, another study by Tanaka and coworkers has demonstrated the importance of SAPK/p38 MAPK activation as a modulator of endothelial cell migration in response to bFGF .
Treatment of HIMEC with neutralizing VEGFR2 antibody abolished the cell migration, which was consistent with the observation that VEGFR2 is a positive regulator of angiogenesis . However, the biochemical events that couple VEGFR2 to p38 MAPK activation and cell migration are still unknown. Studies have shown that VEGFR1 is involved in the down-regulation of the VEGFR2 which is required for angiogenesis . Petrova et al.  demonstrated that VEGFR1 has a higher affinity than VEGFR2 for VEGF and can titrate VEGF by competing with VEGFR2, so at low concentration of VEGF, this will establish a threshold for the onset of angiogenesis and allows a down regulation of signal later in the process .
VEGF stimulation of endothelial cells results in dephosphorylation and translocation of NFATp from the cytoplasm to the nucleus in a time dependent fashion. The calcineurin inhibitor CsA blocked the translocation of NFATp. It has been shown that in T lymphocytes and fibroblasts, elevations of intracellular calcium levels result in calcineurin activation and subsequent activation and nuclear localization of NFAT proteins [37, 38]. These data suggest that VEGF activation of the calcineurin pathway in HIMEC leads to the translocation of NFATp to the nucleus, where it is phosphorylated and then exported to the cytoplasm. Therefore, it appears that NFATp activation in HIMECs is regulated by similar mechanisms like those operating in T cells or fibroblasts.
NFAT proteins are the major targets of the calcineurin inhibitors CsA and FK506, and NFAT activation has been shown to affect the activation of other transcription factors which may in part explain the potent effect of CsA and FK506 as immunosuppressive agents [39, 40]. CsA has been shown to play a role in the expression of cytokines produced by endothelial cells including IL-1, IL-6, and IL-8 in different cell types [41, 42], thus NFAT may be potentially involved in the transcriptional regulation of these cytokine genes in endothelial cells. Our data corroborate previous studies demonstrating that NFAT activation is a key component of the angiogenic response induced by VEGF in endothelial cells , and modulation of this pathway may represent an adverse effect of calcineurin inhibition during transplant immunosuppression. Indeed, an increasing body of evidence suggests that the pharmacologic strategies which effectively inhibit acute rejection, may in fact be playing a central role in the etiogenesis of vascular dysfunction which is central to the pathology of chronic rejection, and is emerging as an important cause of morbidity and mortality in solid organ transplant patients in the years following successful engraftment.
The cyclooxygenase enzymes COX-1 and COX-2 have been shown to play an important role in the regulation of angiogensis . These enzymes catalyze the conversion of arachidonic acid to PGH2, the first step in the biosynthesis of the PGs thromboxane and prostacyclin . In endothelial cells COX-1 is constitutively expressed, whereas COX-2 is inducible in response to various activators such as mitogens, hormones and inflammatory cytokines . The human COX-2 promoter contains binding sites for cAMP response element (CRE), NF-IL6 (C/EBP), and NFκB . An essential role for NFAT in the induction of COX-2 gene by VEGF in HUVEC has been reported . However, these investigators did not evaluate the activation of alternate signaling mechanisms which undergo activation in response to VEGF, specifically the MAPK family members. Our present study confirms that COX-2 and NFAT played an important role in microvascular endothelial angiogenesis induced by VEGF, but in addition demonstrated a differential contribution of p44/42 MAPK and p38 MAPK in various cellular physiologic steps which comprise angiogenesis.
VEGF activation of MAPKs (ERKs, JNKs/SAPKs, and p38 MAPK) signal transduction pathways in endothelial cells [47, 48] are consistent with the VEGF activation of AP-1 that we show here. The MAPKs regulate the AP-1 family members at the transcriptional and posttranscriptional levels [49, 50]. We have shown the induction of AP-1 by the AP-1 DNA-binding activity and the translocation of c-Fos and c-jun from cytoplasm to the nucleus upon VEGF activation of HIMEC. AP-1 DNA binding was not inhibited by CsA. Given the major role of VEGF in physiological and pathological angiogenesis, the identification of NFAT and AP-1 as transcription factors that couple VEGF signaling to the transcriptional gene response may help to localize therapeutic targets to antagonize or modulate the angiogenic process and to further delineate the upstream signaling pathways and the specific gene expression program triggered by VEGF in endothelial cells.
Perhaps the most important finding in our paper, is the demonstration of the differential effect of CsA on distinct signaling pathways which play integral roles in the complex biologic process of angiogenesis. CsA is known to exert specific effects on the intracellular signaling cascades, as previously published data from our laboratory demonstrated that CsA inhibits p38 MAPK activation in response to TNF-α+ LPS activation in HIMECs . We evaluated a series of key steps in VEGF induced angiogenesis, and found that various members of the MAPK family, NFAT, AP-1 and COX-2 played primary roles in different stages of the cell physiology. p38 MAPK played an early role in stress fiber assembly, and also played a key role in endothelial cell migration. Monolayer expansion and proliferation of endothelial cells was dependent on p44/42 MAPK and COX-2. Maturation of microvascular endothelial cells in the context of in vitro tube formation was dependent on p44/42 MAPK, COX-2, NFAT but not p38 MAPK. Our data also demonstrated that NFκB did not play a role in the VEGF induced angiogenic response, nor did c-Fos or c-Jun, the components of AP-1. Integrating the specific effect of CsA on these various stages of angiogenesis has not been previously described. A major challenge in defining the regulation of intracellular cellular activation remains the process of characterizing the simultaneous activation and interaction of signaling cascades and networks. Our data demonstrates that MAPK signaling cascades will be involved in multiple steps in angiogenesis, playing distinct roles sequentially in the process. Finally, we have also demonstrated that the signaling responses in HIMEC were dependent on VEGF concentration, as higher amounts of this growth factor resulted in a paradoxical decrease in activation, a phenomenon previously described for the angiogenic chemokines [51, 14, 29].
Our study demonstrates that different signaling pathways will play dominant roles in individual steps which are involved in a complex biologic process, such as angiogenesis. The use of complementary in vitro assays for the assessment of angiogenesis allowed us to characterize the signaling pathways which were interacting during VEGF activation. If only one assay had been emphasized, the overall interplay of signaling cascade activation would not have been appreciated. At the present time, there is intense interest in defining the ability of signaling cascades to interact in a coordinated fashion, and likewise, an attempt to characterize the effect of pharmacologic agents on cellular activation.
There are important clinical ramifications which can be envisioned related to the observations in our study. Pharmacologic approaches using CsA and COX-2 inhibition may exert potent effects on blood vessels, which are underappreciated at the present time. The importance of angiogenesis in neoplastic disease and wound healing are two immediate areas where these pharmacologic agents may exert beneficial, or potentially deleterious effects. Studies focusing on organ specific microvascular populations may help in determining new clinical indications for the use of pharmacologic agents targeting blood vessels.
In summary, CsA exerts potent effects on human microvascular endothelial cells, inhibiting all of the stages of in vitro angiogenesis which were evaluated. More importantly, the effect of CsA was exerted through differential inhibitory effects on an interplay of signaling cascades, which contributed to distinct components of angiogenesis, including stress fiber assembly, migration, endothelial monolayer expansion and proliferation, and tube formation. Our data suggests that CsA exerts potent effects on non-immune vascular cell populations which may contribute to microvascular dysfunction and the vasculopathy which characterizes chronic rejection following solid organ transplantation. Our findings might help explain the limited clinical success of human small intestinal transplantation, as the calcineurin inhibitors required for post-transplant immunosuppression adversely affect angiogenic and vascular homeostatic mechanisms in intestinal microvascular endothelial cells. Finally, defining the effect of the calcineurin inhibitors on human microvascular endothelial cells may ultimately open the route for novel anti-angiogenic strategies using these agents as inhibitors of vessel proliferation for therapeutic benefit, potentially as adjunctive treatments of adenocarcinoma.
Material and Methods
Antibodies and reagents
VEGF and anti-human VEGF antibodies (VEGFR1 and VEGFR2) were from R&D Systems (Minneapolis, MN). Cyclosporine A (CsA) was from Alexis (San Diego, CA). Rapamycin, FK506 and the MAPK inhibitors (PD098059, SB203580) were obtained from Calbiochem (La Jolla, CA). The selective COX-2 inhibitor NS398 was from Cayman Chemical Co. (Ann Arbor, MI). Antibodies against the MAPK superfamily members (p44/42 MAPK, p38 MAPK, and c-jun NH2-terminal MAPK (SAPK)) were from New England Biolabs (Beverly, MA). Antibodies to NFAT, p65 subunit of NF-κB and COX-1/-2 were obtained from Santa Cruz Biotechnology (Santa Cruz, CA). Fluorescein-conjugated phalloidin was from Molecular Probes, Inc. (Eugene, OR). Fluorescein-conjugated streptavidin was from Pierce (Rockford, IL). Endothelial Cell Growth Supplement (ECGS) was from Upstate Biotech Inc. (Lake Placid, NY). MCDB-131 medium, porcine heparin, PSF (penicillin/streptomycin/fungizone), and soybean trypsin inhibitor were from Sigma (St. Louis, MO). Fetal bovine serum (FBS) was from Bio Whittaker (Walkersville, MD). Collagenase type II was from Worthington Biochemical Corporation (Lakewood, NJ), and bovine serum albumin (BSA, Fraction V) was obtained from Fisher Scientific (Fair Lawn, NJ). Human plasma fibronectin was from Chemicon International (Temecula, CA). Oligonucleotide and primers were from Operon (Alameda, CA).
Primary culture of human intestinal microvascular endothelial cells (HIMEC)
Macroscopically normal small intestinal specimens for HIMEC isolation were obtained from patients undergoing scheduled bowel resection. The use of human tissues was approved by the Institutional Review Board of the Medical College of Wisconsin. HIMEC were isolated from surgical specimens and maintained as described earlier . HIMEC cultures were recognized by microscopical features and modified lipoprotein uptake (Dil-ac-LDL, Biomedical Technology, Inc., Stoughton, MA) and expression of Factor VIII-associated antigen. All experiments were carried out using primary endothelial cell cultures between passages 8–12.
Endothelial cell chemotaxis assay
Chemotaxis assay was carried out as described earlier . Briefly, using polycarbonate filters (8 μm pore size, Becton Dickinson Labware, Franklin Lakes, NJ) 5 × 105 cells were added to the upper chamber, and chemotaxis buffer (1000 μl) containing VEGF (1–50 ng/ml) was filled into the lower compartment of the 12-well plates. After 3 hr of incubation at 37°C, cell culture inserts were removed, wiped and stained with DiffQuik (Baxter Scientific, McGraw, IL). Migrated HIMEC adherent to the lower side of the membrane were counted (ten random high-power-fields (HPF; 40×) per condition in a blinded fashion). In inhibition studies, resuspended cells were incubated with neutralizing anti-VEGFR2 antibody, isotype control antibody, CsA (0.1 μM), FK506 (50 nM), Rapamycin (20 nM), SB203580 (5 μM), PD098059 (10 μM) or the selective COX-2 inhibitor, NS398 (10 μM), for 30 min at 37°C. Cell viability was >95% as assessed by trypan blue exclusion. Each condition was assessed in triplicate.
Cell proliferation assay
3× 104 HIMEC per well were seeded onto fibronectin-coated 24-well plates using growth medium without ECGS as described earlier . After pre-treatment with the indicated inhibitors (CsA 0.1 μM, PD098059 10 μM, SB230580 5 μM, NS398 10 μM) for 30 min at 37°C, cells were stimulated with VEGF (50 ng/mL) for 24, 48, and 72 hr, or left untreated. Following complete detachment, cells were re-suspended and counted in a Coulter Counter (Coulter, Brea, CA). In parallel experiments, cell viability was assessed by trypan blue exclusion and was greater than 95%. Each condition was assessed in triplicate.
Cellular DNA synthesis was assessed by 3H-thymidine uptake in HIMEC as described earlier . HIMEC were pulsed with 3H-thymidine (1 μCi/ml; Amersham, Arlington Heights, IL), washed twice on ice with 5% (v/v) trichloroacetic acid prior to fixation. DNA was then released from precipitated material by alkaline lysis in 0.5 N NaOH, and supernatants were quantified in a beta-counter. Each condition was assessed in triplicate.
Microscopic wounding assay
To assess HIMEC migration in response to angiogenic stimuli, a microscopic wounding assay was performed as described earlier . In brief, a HIMEC confluent monolayer was scraped along a straight line, and the remaining monolayer was then incubated with growth medium (without ECGS), and cells were pretreated for 30 min at 37°C with or without CsA (0.1 μM), SB203580 (5 μM) or PD098059 (10 μM). Then, cells were stimulated by addition of VEGF (10 ng/ml) or left untreated. The migration of HIMEC across the demarcation line was monitored using an inverted microscope. At each time point (24, 48, and 72 hr), 10 random fields using an ocular grid were counted in a blinded fashion. Data were expressed as cells/mm2, and each condition was assessed in triplicate.
Matrigel™ in vitro-tube formation assay
Endothelial tube formation was assessed using Matrigel™, a solubilized extracellular basement membrane matrix extracted from the Engelbreth-Holm-Swarm mouse sarcoma, as described previously . HIMEC resuspended in complete growth medium which were seeded at a density of 5 × 104 cells per well. Where indicated, the growth medium was supplemented with CsA (0.1 μM), PD098059 (10 μM), SB203580 (5 μM) and NS398 (10 μM). Control wells contained no inhibitors. Endothelial tube formation on Matrigel™ after 16 hr was assessed by inverted phase contrast microscopy and photographed with an inverted tissue culture microscope. Five high power fields per condition were examined and experiments were repeated in two independent HIMEC cultures.
Cellular fractionation and western blot analysis
Confluent HIMEC monolayers in 35-mm culture dishes (one dish per condition) were pre-treated with various inhibitors for 30 min or left untreated before VEGF activation (50 ng/ml) for different time periods (1, 5,10, 15, 20, 30, 60, and 120 min) as described previously . The homogenates were centrifuged and supernatants (cytosolic fraction) were removed and protein concentrations were determined using a Bradford Assay (Bio-Rad, Hercules, CA). Equal amounts of protein were separated by SDS-PAGE and transferred to nitrocellulose membranes . The membranes were blocked for 3 hr at room temperature in 3% (w/v) BSA, 3% (w/v) nonfat dry milk in Tris-buffered saline (50 mM Tris-HCl, 150 mM NaCl, pH 7.4) containing 0.1% (v/v) Tween 20(TBS-T), then were incubated with specific primary antibodies to NFATp, COX-2, phosphorylated and non-phosphorylated MAPK (ERK1/2, p38 MAPK and JNK) at 4°C overnight as specified. Detection was by secondary antibody coupled to horseradish peroxidase (HRP) and ECL™ (Amersham Pharmacia Biotech; Arlington Heights, IL).
Electrophoretic mobility shift assay (EMSA)
Nuclear protein extraction was performed as described previously . In brief, HIMEC monolayers were lysed in hypotonic lysis buffer and cell nuclei were collected and frozen immediately in liquid nitrogen until further usage. Protein concentrations were determined using a Bradford assay (Bio-Rad, Hercules, CA). The samples were then incubated on ice with 32P-labeled double stranded oligonucleotide for 30 min and DNA-protein complexes were separated by SDS-PAGE. Dried gels were exposed to X-ray film to detect DNA binding of NFAT, NF-κB and AP-1. The synthetic oligonucleotides  used as probes in electrophoretic mobility shift assays (EMSAs) were as follows: NFAT; 5'-tcgaCAAGGGGAGAGGAGGGAAAAATTTGTGGC-3' (nucleotides -117 to -91 containing the NFAT site of the human COX-2 promoter); NF-κB; 5'-gatcAGTGGGGACTACCCCCT-3' (nucleotides -277 to-211 containing the NF-κB site of the human COX-2 promoter) and for AP-1; 5'-tcgaCAAAAGGCGGAAAGAAACAGTCATTTC-3' (nucleotides -82 to -58 containing the NFAT-AP1 site of the human Cox-2 promoter).
F-Actin polymerization was assessed in subconfluent HIMEC seeded on fibronectin-coated glass chamber slides (LabTek; Nalge Nunc, Naperville, IL) as described previously . Cells were cultured in MCDB-131 without FBS for 12 hr and pretreated for 30 min at 37°C with or without CsA (0.1 μM), SB203580 (5 μM) or PD098059 (10 μM). HIMEC were then stimulated with 10–50 ng/ml recombinant human VEGF (1–15 min), and fixed with 3.7% (v/v) formaldehyde in PBS for 20 min at room temperature. Cells were washed and permeabilized with Triton X-100 (0.1% (v/v) in PBS) for 10 min, blocked with 2.5% (w/v) BSA/PBS, and stained with fluorescein-phalloidin (Molecular Probes, Eugene, OR). After washing, slides were air dried and mounted with Fluoromount-G (Southern Biotechnology, Birmingham, AL) and examined with a fluorescence microscope (Olympus BX-40) using a fixed shutter speed to allow for comparison of fluorescence intensity. In some experiments, stress fiber assembly was blocked by pre-incubation of cells with 10 μg/ml VEGFR2 antibody, (30 min at 37°C).
For immunofluoresence staining to demonstrate translocation of NFAT, p65 (NF-κB subunit), c-Jun and c-Fos (AP-1 subunit), cells were grown as above, left untreated or pre-treated with CsA (0.1 μM) before VEGF (50 ng/ml) or TNF-α/LPS (TNF-α 100 units/ml, LPS 1 μg/ml) for 30 min. Cells were then fixed with 3% (w/v) paraformaldehyde in phosphate-buffered saline (PBS) for 15 min at room temperature and washed three times (5 min each) with washing buffer (PBS, 0.01% (v/v) Nonidet P-40 [NP-40]). After blocking for 30 min as above, the cover slips were incubated with the anti-NFATp, p65, c-Jun, phospho-c-Jun and c-Fos antibodies for 60 min at room temperature. Unbound antibody was removed by rinsing three times with washing buffer and the cover slips were incubated for 30 min with a fluorescein-conjugated secondary antibody (Santa Cruz), washed three times, mounted and visualized as above.
RNA preparation and semi-quantitative RT-PCR
Human COX-1, COX-2 and Bata-actin primers
COX-1 forward (5'-TGCCCAGCTCCTGGCCCGCCGCT-3')
COX-1 reverse (5'-TTCAAATGAGATTGTGGGAAAATTGTC-3')
COX-2 forward (5'-TCAAATGAGATTGTGGGAAAATTG-3')
COX-2 reverse 5'-TCTAGTAGAGACGGACTCATAGAA-3')
β-actin forward (5'-CCAGAGCAAGAGAGGCATCC-3')
β-actin reverse (5'-CTGTGGTGGTGAAGCTGTAG-3')
Analysis of data
Statistical Analysis was performed using Statview 4.5 and superANOVA software for the Macintosh. When single comparisons were made, t-tests were used, applying paired or unpaired analysis as appropriate. When multiple comparisons between groups were performed one way or two-way analysis of variance was used as appropriate followed by the Student-Newman Keuls test. P ≤ 0.05 was considered significant.
human intestinal microvascular endothelial cells
mitogen-activated protein kinases
stress activated protein kinase/c-Jun kinase
extracellular signal-regulated kinase
tumor necrosis factor alpha
nuclear factor kappa B
nuclear factor of activated T cells
We thank H. Brandenburg for expert assistance in preparation of the manuscript. This work was supported by the Medical College of Wisconsin Cancer Center (P.R., D.G.B., M.F.O.), the National Institute of Health grants DK 057139, the Crohn's and Colitis Foundation of America and the Digestive Disease Center and Cancer Center of the Medical College of Wisconsin (D.G.B., P.R.).
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