Connective tissue growth factor (CTGF, a.k.a. CCN2) is inflammatory mediator and abundantly expressed in osteoarthritis (OA). Angiogenesis is essential for OA progression. Here, we investigated the role of CTGF in vascular endothelial growth factor (VEGF) production and angiogenesis in OA synovial fibroblasts (OASFs). We showed that expression of CTGF and VEGF in synovial fluid were higher in OA patients than in controls. Directly applying CTGF to OASFs increased VEGF production then promoted endothelial progenitor cells tube formation and migration. CTGF induced VEGF by raising miR-210 expression via PI3K, AKT, ERK, and nuclear factor-κB (NF-κB)/ELK1 pathways. CTGF-mediating miR-210 upregulation repressed glycerol-3-phosphate dehydrogenase 1-like (GPD1L) expression and PHD activity and subsequently promoted hypoxia-inducible factor (HIF)-1α-dependent VEGF expression. Knockdown of CTGF decreased VEGF expression and abolished OASF-conditional medium-mediated angiogenesis in vitro as well as angiogenesis in chick chorioallantoic membrane and Matrigel-plug nude mice model in vivo. Taken together, our results suggest CTGF activates PI3K, AKT, ERK, and NF-κB/ELK1 pathway, leading to the upregulation of miR-210, contributing to inhibit GPD1L expression and prolyl hydroxylases 2 activity, promoting HIF-1α-dependent VEGF expression and angiogenesis in human synovial fibroblasts.
Osteoarthritis (OA) refers to clinical syndrome of joint pain accompanied by varying degrees of functional limitation and reduced quality of life.1 Cause of the OA is unclear, although obesity, aging, sex, genetic factors, and injury have been associated with increased risk of OA.2 Development and progression of OA are now believed to involve synovial inflammation even in early stages of the disease.3 Biochemical mediators like cytokines, chemokines, and growth factors were found in OA synovial fibroblasts (OASFs) that affect cellular functions of knee joints. These mediators promote inflammation, cartilage degradation, and neovascularization via activation of angiogenetic factors like vascular endothelial growth factor (VEGF),4,5 reportedly secreted from mechanically overloaded chondrocytes6 and in OA joints in vivo.7 VEGF also affects chondrocytic metabolism, leading to release of matrix metalloproteinases that degrade cartilage matrix.8 Anti-VEGF polyclonal antibody markedly attenuated disease severity in arthritis,9 indicating anti-angiogenesis as novel OA treatment.
Connective tissue growth factor (CTGF, a.k.a. CCN2) is a member of the CCN family, secreted multifunctional proteins that contain high levels of cysteine. It has been proven associated with several biological functions such as fibrosis, tissue remodeling, and tumorgenesis even to OA.10 The mRNA expression of CTGF has been upregulated adjacent to areas of cartilage surface damage, and present in chondro-osteophytes.11 In animal model, CTGF overexpression in synovial lining of mouse knee joints results in reversible synovial fibrosis and cartilage damage.12 Both plasma and synovial fluid CTGF concentration in OA patients were correlated with radiographic severity and could be useful for monitoring progression of OA.13 We previously indicated CTGF enhancing IL-6 and MCP-1 expression and promoting inflammation in OASFs,14,15 meaning CTGF contributes to pathogenesis of OA.
The small, noncoding microRNAs (miRNAs) transcribed from DNA are 18–24 nucleotides in length, modulating targeted gene expression via either translational repression or mRNA cleavage.16 It is recently reported that miRNA expression was associated with well-defined clinical pathological features and disease outcomes;17,18 miRNAs also have been linked with OA pathogenesis, especially for expression of genes encoding catabolic factors like matrix metalloproteinases and ADAMTS.19 Many evidences indicated that miR-210 as angiogenic miRNA.20, 21, 22 In addition, overexpression of miR-210 can stimulate formation of capillary-like structures in vitro when cells are cultured in Matrigel.23 However, the exact etiological mechanism of miR-210 in angiogenesis and OA pathogenesis is largely unknown.
Angiogenesis is essential for the development, growth, and progression of OA.24 VEGF, a potent angiogenic factor, is pivotal in OA pathogenesis.7 CTGF is cited as promoting inflammatory cytokine release during OA;12 its role in angiogenesis is implied in many cell types,25,26 but its signal pathway in VEGF production and angiogenesis in synovial fibroblasts has not been extensively studied. We explored intracellular signal pathway in CTGF-induced VEGF production in OASFs and found CTGF activating PI3K, AKT, ERK, and nuclear factor-κB (NF-κB)/ELK1 pathway to upregulate miR-210 expression and contributing to inhibit GPD1L expression and prolyl hydroxylases 2 (PHD2) activity as well as trigger HIF-1α-dependent VEGF expression and angiogenesis in human OASFs.
CTGF promotes VEGF-dependent angiogenesis in synovial fibroblasts
CTGF is associated with OA pathogenesis.12 VEGF is most potent pro-angiogenic growth factor playing a pivotal role in angiogenesis.4,27 We first examined CTGF and VEGF expression in OA and normal synovial fluid to find expression of CTGF and VEGF in synovial fluid significantly higher in OA patients than in controls (Figure 1a). On the other hand, medium from OASFs exhibited significant CTGF and VEGF levels, higher than that of medium from normal SFs (Figure 1a). Expression of CTGF positively correlated with VEGF (Figure 1b). Angiogenesis mainly involves endothelial cell proliferation, migration, and tube formation to form new blood vessels.28 We also found OA synovial fluid or OASF conditioned medium (CM) enhancing endothelial progenitor cell (EPC) tube formation and migration (Figures 1c and d), suggesting CTGF and VEGF have key roles in OA angiogenesis and pathogenesis.
Next, we directly applied CTGF in OASFs and determined the expression of VEGF; CTGF raised VEGF mRNA and protein expression in a concentration- (Figures 2a and b) and time-dependent manner (Figures 2c and d). Likewise, CM from CTGF-treated OASFs promoted tube formation and migration in EPCs by concentration- and time-dependently (Figures 2e–h). To elucidate CTGF-dependent VEGF’s lead role in angiogenesis, VEGF antibody was used. Figures 2e–h show pretreatment of OASFs with VEGF antibody significantly abolished CTGF-induced tube formation and migration of EPCs (Figures 2e–h), indicating CTGF-dependent VEGF expression promotes OASF angiogenesis.
CTGF promotes VEGF production and angiogenesis by increasing miR-210 via PI3K, AKT, and ERK pathways
Several miRNAs identified show differential expression patterns between OA and normal patients; their postulated functions relate to inflammatory, catabolic changes, and angiogenesis during OA process.29,30 To probe miRNA differential expression in CTGF-treated OASFs, we used a customized array of 96 human miRNAs. Three were significantly upregulated and three were downregulated (Supplementary Figure 1). Among significantly regulated miRNAs, miR-210 was most upregulated in CTGF-treated OASFs compared with controls. We directly applied CTGF in OASFs to rate miR-210 expression, which miR-210 raised in a time-dependent manner (Figure 3a). We also found miR-210 expression in OASFs sharply higher than in normal SFs (Supplementary Figure 2). To verify direct CTGF inducement of miR-210-mediating VEGF-dependent angiogenesis, we transfected miR-210 mimic or inhibitor into OASFs; miR-210 inhibitor but not mimic blocked CTGF-induced VEGF expression, EPC tube formation and migration (Figures 3b–d). These suggest miR-210 as positive regulator of CTGF-mediated, VEGF-dependent angiogenesis in OASFs.
PI3K, AKT, and ERK pathways are reported to regulate expression of miR-210 and VEGF.31, 32, 33 We assessed their roles in CTGF-induced miR-210 and VEGF expression. CTGF treatment of OASFs induced time-dependent phosphorylation of all three (Figure 3e). Pretreatment with PI3K (Ly294002 or Wortmannin), AKT (AKTi), and ERK inhibitors (U0126 or PD98059) for 30 min reduced CTGF-induced miR-210 expression (Figure 3f). Yet all of them suppressed CTGF-mediated VEGF production and EPC tube formation and migration (Figures 3g–i). Results portend CTGF acting via PI3K, AKT, and ERK signaling pathways to promote miR-210 expression and VEGF-dependent angiogenesis in human synovial fibroblasts.
Involvement of NF-κB and ELK1 in CTGF increases miR-210 upregulation
The miR-210 promoter contains NF-κB- and ELK1-binding sites.34 To determine which transcription factors are involved in CTGF-induced miR-210 expression, three different length miR-210 promoter constructs were generated. Figure 4a shows that CTGF significantly increased phmiR210-Luc (−1033/+86) promoter activity, which was partially reduced in phmiR210-Luc (−297/+86; deletion ELK1-binding site) construct and completely abolished in phmiR210-Luc (−35/+86; deletion ELK1- and NF-κB-binding sites) construct. The role of NF-κB and ELK1 was further established using the NF-κB inhibitor (PDTC) and IκB protease inhibitor (TPCK) or ELK1 and p65 small interfering RNA (siRNA). Figure 4b shows all these inhibitors or siRNAs markedly reducing CTGF-induced miR-210 expression. With CTGF-mediated VEGF expression or EPC tube formation and migration reduced by transfection with ELK1 and p65 siRNA (Figures 4c–e), we postulate CTGF-increased miR-210 upregulation and angiogenesis as involving NF-κB and ELK1 transactivation.
We further explored whether these signaling pathways are upstream molecules in CTGF-induced NF-κB and ELK1 transcriptional activation. Pretreatment of cells with Ly294002, Wortmannin, AKTi, U0126, and PD98059 abolished CTGF-increased p-p65 and p-ELK1 accumulation into nuclei as well as p65 and ELK1 binding to NF-κB and ELK1 elements on miR-210 promoter (Figures 4f and g). CTGF thus increases VEGF-dependent angiogenesis by augmenting miR-210 expression through PI3K, AKT, ERK, and NF-κB/ELK1 signaling pathways in human synovial fibroblasts.
CTGF promotes HIF-1α-dependent VEGF expression and angiogenesis by inhibiting GPD1L expression and PHD2 activity via upregulating miR-210
To identify mechanism of miR-210-involved VEGF-dependent angiogenesis, we searched for downstream genes using bioinformative screening analysis of miRNA target databank: TargetScan, MicroCosm, and miRanda. From these three databanks overlapping between predicted targets of miR-210, GPD1L ranked as most probable target. We used luciferase reporter vectors harboring wild-type 3'-untranslated region (3′UTR) of GPD1L mRNA (wt-GPD1L-3′UTR) and vector containing mismatches in predicted miR-210-binding site (full muntant-GPD1L-3′UTR) to learn if miR-210 regulates 3′UTR of GPD1L. Figure 5a shows CTGF and miR-210 mimic inhibiting luciferase activity in wt-GPD1L-3′UTR plasmid but not in muntant-GPD1L-3′UTR plasmid. On the other hand, miR-210 inhibitor reversed CTGF-inhibited GPD1L mRNA and protein expression (Figure 5b). Therefore, miR-210 directly represses GPD1L expression through binding to 3′UTR of human GPD1L gene.
GPD1L is reported to potentiate activation of PHD2, further ensuring hypoxia-inducible factor 1α (HIF-1α) hydroxylation, and leading to decrease HIF-1α expression.34 It has been reported that HIF-1α hydroxylation at Pro-564 represents PHD2 activity.35 CTGF-inhibited HIF-1α hydroxylation was reversed by miR-210 inhibitor, leading to decrease the accumulation of HIF-1α into nucleus (Figure 5c), indicating CTGF-mediated miR-210 upregulation inhibits PHD2 expression and subsequently increases HIF-1α activation. To investigate the role of GPD1L and PHD2 in accumulation of HIF-1α into nucleus, the GPD1L and PHD2 siRNA were used. Transfection of GPD1L and PHD2 siRNA significantly reduced HIF-1α hydroxylation and increased accumulation of HIF-1α into nucleus (Supplementary Figure 3A). Furthermore, these siRNAs also increased EPC tube formation and migration ability (Supplementary Figures 3B and C). Next, we sought to investigate whether HIF-1α was involved in CTGF-induced VEGF expression in human synovial fibroblasts. We found that pretreatment with HIF-1α inhibitor diminished CTGF-promoted VEGF production, EPC tube formation and migration (Figures 5d–f). These suggest CTGF boosting HIF-1α-dependent VEGF expression and angiogenesis by inhibiting GPD1L expression and PHD2 activity through upregulation of miR-210.
Knockdown of CTGF impairs angiogenesis in vitro and in vivo
To confirm CTGF-mediated VEGF-dependent angiogenesis, CTGF-shRNA was transfected into OASFs, thus reducing CTGF and VEGF expression (Figure 6a). CTGF-shRNA also abolished OASF CM-mediated EPC tube formation and migration (Figures 6b and c). Effect of CTGF on angiogenesis in vivo was evaluated by in vivo model of chicken chorioallantoic membrane (CAM) assay. CM from OASFs increasing angiogenesis in CAM was clearly observed (Figure 6d). By contrast, knockdown of CTGF precipitously reduced angiogenesis (Figure 6d). We also analyzed Matrigel plug formation following subcutaneous implantation in mice. Matrigel mixed with CM from OASFs increased blood vessel growth (Figure 6e). Accordingly, CM from OASFs/CTGF-shRNA cells significantly curtailed neovascularization (Figure 6e). Knockdown of CTGF diminished microvessel formation in Matrigel plugs by analyzing CD31 stain and hemoglobin level (Figure 6e). Overall results indicate CTGF promoting angiogenesis in vivo.
OA is a heterogeneous group of conditions associated with defective integrity of articular cartilage as well as related changes in underlying bone. Neovascularization, formation of new blood vessels, can maintain chronic inflammatory status by transporting inflammatory cells to site of synovitis as well as supplying nutrients and oxygen to pannus.36,37 VEGF is a major angiogenic factor in OA joints.38 On the other hand, CTGF is involved in OA pathogenesis;12,14 its effect on VEGF expression and angiogenesis in human synovial fibroblasts is mostly unknown. Our study found expression of CTGF and VEGF in synovial fluid significantly higher than normal in OA patients, using ELISA assay. We further identified VEGF as a target protein for CTGF signaling pathway that regulates angiogenesis. Treatment of OASFs with CTGF increased VEGF expression, later inducing migration and tube formation of human EPCs. OASF CM-mediated tube formation and angiogenesis was abolished by CTGF shRNA. In addition, CTGF knockdown reduced angiogenesis in vivo. Our study suggests CTGF raising VEGF expression and promoting angiogenesis in human OASFs. One mechanism underlying CTGF increased VEGF yield by activating PI3K, AKT, ERK, and NF-κB/ELK1 pathway, thus upregulating miR-210 expression.
The small, noncoding miRNAs regulate gene expression at post-transcriptional level by either degradation or translational repression of a target mRNA that regulates physiological and pathological processes.39 They and their multiple target genes reportedly play key roles in gene regulation and contribute to OA pathogenesis.40 It was revealed that miR-146,41 miR-155,42 and miR-20343 regulate arthritic inflammatory response. We screened 96 miRNAs from customized miRNA array to find miR-210 most upregulated in CTGF-treated OASFs. Also, qPCR confirmed expression of miR-210 in OASFs starkly higher than in normal SFs, indicating that miR-210 promotes angiogenesis.44 We saw OASF transfection with miR-210 inhibitor reducing CTGF-induced VEGF production as well as EPC tube formation and migration, making it an angiogenic gene in human OASFs. It is a direct target for ephrin-A3, protein-tyrosine phosphatase 1B, ETS domain-containing protein (ELK3), and thrombospondin that regulate angiogenesis.45,46 We use miRNA target prediction (TargetScan, MicroCosm, and miRanda) to find GPD1L as most probable miR-210 target, whereas CTGF decreased GPDlL mRNA expression. Transfection of miR-210 inhibitor significantly reversed CTGF-inhibited GPD1L expression. We also indicated that miR-210 directly repressed GPD1L protein expression through binding to 3′UTR of human GPD1L gene, thereby negatively regulating GPD1L that is documented as promoting PHD activity and later impeding HIF-1α expression.34 We proved CTGF increases accumulation of HIF-1α into nuclei as inhibited by miR-210 inhibitor, thus promoting HIF-1α-dependent VEGF expression and angiogenesis by inhibiting GPD1L expression and PHD2 activity via miR-210 upregulation.
PI3K, AKT, and ERK as potential candidate signaling molecules have shown capacity for regulating the VEGF expression and proliferation of endothelial cells.47,48 On the other hand, PI3K, AKT, and ERK reportedly regulate miR-210 expression.33 CTGF incubation of OASFs enhanced phosphorylation of PI3K, AKT, and ERK. Pretreatment with PI3K, AKT, or ERK inhibitors antagonized the increase of VEGF production and angiogenesis by CTGF. These inhibitors antagonized CTGF-increased miR-210 expression, indicating CTGF-increased VEGF-dependent angiogenesis via PI3K, AKT, ERK, and miR-210 signaling pathways. Angiogenesis contributes to synovitis, osteochondral damage, osteophyte formation, and meniscal pathology in OA patients. VEGF is a potent angiogenic factor pivotal in OA pathogenesis. CTGF activates PI3K, AKT, ERK, and NF-κB/ELK1 pathway, leading to the upregulation of miR-210, contributing to inhibit the GPD1L expression and PHD2 activity, promoting the HIF-1α-dependent VEGF expression and angiogenesis in human synovial fibroblasts (Figure 7). This may lend understanding of synovial angiogenesis mechanisms to yield effective therapy.
Materials and Methods
Rabbit polyclonal antibodies specific to p-p85, p-AKT, p-ERK, p-p65, and p-ELK1 were purchased from Cell Signaling Technology (Danvers, MA, USA); rabbit polyclonal antibodies specific to p85, AKT, ERK, p65, ELK1, PCNA, PHD2, and the siRNAs against PHD2 and a control for experiments using targeted siRNA transfection (each consists of a scrambled sequence that does not lead to specific degradation of any known cellular mRNA) from Santa Cruz Biotechnology (Santa Cruz, CA, USA); CD31, GPD1L, and OH-HIF-1α (Pro564) antibody from Abcam (Cambridge, MA, USA); recombinant human CTGF and VEGF ELISA kit from PeproTech (Rocky Hill, NJ, USA); Ly294002, Wortmannin, U0126, and PD98059 from Enzo Biochem, Inc. (New York, NY, USA); miR-210 mimic, miR-210 inhibitor, Lipofectamine 2000, and Trizol from Life Technologies (Carlsbad, CA, USA). The customized miRNA array primer was obtained from System Biology Ireland (Galway, Ireland); DMEM, α-MEM, fetal bovine serum (FBS), and all other cell culture reagents from Gibco-BRL Life Technologies (Grand Island, NY, USA); wild-type 3′UTR of GPD1L mRNA (wt-GPD1L- 3′UTR) and vector containing mismatches in predicted miR-210-binding site (full muntant-GPD1L-3′UTR) from Addgene (Cambridge, MA); ON-TARGETplus siRNAs of ELK1, p65, GPD1L and control from Dharmacon Research (Lafayette, CO, USA); all other chemicals Sigma-Aldrich (St. Louis, MO, USA).
Human synovial fibroblasts were isolated by collagenase treatment of synovial tissue samples obtained from patients with OA during knee replacement surgery and samples of non-arthritic synovial tissues obtained at arthroscopy after trauma/joint derangement at China Medical University Hospital. Protocol for study was approved by the Institutional Review Board at China Medical University Hospital and informed consent was obtained from each donor. OASFs were isolated, cultured, and characterized as previously described.49 Human endothelial progenitor cells (EPCs) were approved by the Institutional Review Board of Mackay Medical College at New Taipei City, Taiwan (reference number: P1000002). All subjects gave written consent before enrollment. Briefly, CD34-positive EPCs were maintained and propagated in MV2 complete medium consisting of MV2 basal medium and growth supplement (PromoCell, Heidelberg, Germany) of 20% FBS (HyClone, Logan, UT, USA). Cultures seeded onto 1% gelatin-coated plasticware were maintained at 37 °C in a humidified atmosphere of 5% CO2.50
Western blot analysis
Lysates were prepared as described previously,51 proteins resolved by SDS-polyacrylamide gel electrophoresis and transferred to Immobilon polyvinyl difluoride membranes (Immobilon P, Millipore, Billerica, MA, USA). Blots blocked with 4% BSA for 1 h at room temperature were probed with rabbit anti-human antibodies against PI3K, AKT, ERK, p65, and ELK1 (1 : 1000) for 1 h at room temperature. After third wash, blots were incubated for 1 h at room temperature with donkey anti-rabbit peroxidase-conjugated secondary antibody (1 : 3000), then visualized by enhanced chemiluminescence with Kodak X-OMAT LS film (Eastman Kodak, Rochester, NY, USA).
Real-time quantitative PCR (RT-qPCR) of mRNA and miRNA
Total RNA was extracted from human synovial fibroblasts by TRIzol; reverse transcription used 1 μg of total RNA transcribed into cDNA by oligo (dT) primers.49 RT-qPCR used Taqman One-Step RT-PCR Master Mix (Applied Biosystems, Foster City, CA, USA): 2 μl of cDNA template added to each 25-μl reaction with Taqman probes and sequence-specific primers. Sequences for target gene primers and probes were purchased commercially. Glyceraldehyde 3-phosphate dehydrogenase served as an endogenous control to normalize expression data (Applied Biosystems), qPCR assays carried out in triplicate in a StepOnePlus sequence detection system(Applied Biosystems). The cycling conditions: initial 10-min polymerase activation at 95 °C, followed by 40 cycles at 95 °C for 15 s and 60 °C for 60 s, threshold set above non-template control background and within linear phase of target gene amplification to calculate cycle number at which transcript was detected (denoted CT). For miRNA assay, cDNA was synthesized from total RNA (100 ng) by TaqMan MicroRNA Reverse Transcription Kit (Applied Biosystems). Reactants were incubated at 16 °C for 30 min, then 42 °C for 30 min, followed by inactivation at 85 °C for 5 min. Reactions were then incubated in a 96-well plate at 50 °C for 2 min, 95 °C for 10 min, followed by 30 cycles of 95 °C for 15 s and 60 °C for 60 s with StepOnePlus sequence detection system. Relative gene expression quantification used endogenous control gene (U6). Threshold cycle (CT) was defined as fractional cycle number at which fluorescence passed a fixed threshold, relative expression calculated by comparative CT method.
Measurements of VEGF yield
Human synovial fibroblasts were cultured in 24-well culture plates. After reaching confluence, cells were treated with CTGF, then incubated in humidified incubator at 37 °C for 24 h. To examine downstream signaling pathways involved in CTGF treatment, cells were pretreated with various inhibitors for 30 min before CTGF (10 ng/ml) administration. After incubation, medium was removed and stored at −80 °C until VEGF (in medium) was assayed by VEGF enzyme immunoassay kit, according to the procedure described by the manufacturer.
Plasmids and constructs
Plasmid pGL2-Basic (Promega, Madison, WI, USA) was used to generate constructs of the human miR-210 (hmiR-210) promoter. To obtain phmiR-210 (phmiR210-Luc), which covered positions −1033 to +86, DNA fragments were amplified by PCR with chemically synthesized oligonucleotides that corresponded to nucleotides −1033 to −1015 of the sense strand 5′-IndexTermGGAGATCTAAGACCCCTGAGCCCTTG-3′, and +68 to +86 of the antisense strand 5′-IndexTermCGGCTAGCCGCTGTCACACGCACAGT-3′. Human genomic DNA derived from a healthy adult was used as the template. The PCR products were digested with NheI and BglII and cloned into the NheI-BglII site of pGL2-Basic. The phmiR-210 deletion ELK1-binding site (phmiR210-Luc, −297/+86) or both deletion ELK1- and NF-κB-binding site construct (phmiR-210-Luc, −35/+86) all made by using the sense PCR primers (5′-IndexTermGGAGATCTCTGAGGGACCAGGTCATTTG-3′ and 5′-IndexTermGGAGATCTCAGTGCAATGATGAAAGGGCAT-3′, respectively). All the sense primers have a BglII site at 5′ end of the primer. The PCR products were digested with NheI and BglII and cloned into the NheI-BglII site of pGL2-Basic.
This proceeded as earlier detailed:52 DNA immunoprecipitated with anti-p65 or ELK1 Ab purified and extracted into pellets with phenol-chloroform, then subjected to PCR, products resolved by 1.5% agarose gel electrophoresis and visualized with UV light. Primers 5′-IndexTermACGCGGGTGCGGGGCACGGAGGC-3′ and 5′-IndexTermCGGATGGTACGGCCCGAGGTGG-3′ served to amplify across human miR-210 promoter region contain ELK1-binding site (−595 to −582), primers 5′-IndexTermGGGCCGGGGGGCGAGAGGGTGCCA-3′ and 5′-IndexTermTCCCCTCCAACTTGGGCGTCCGAG-3′ to amplify across human miR-210 promoter region containing ELK1-binding site (−123 to −113).
Human synovial fibroblasts plated in six-well dishes were grown to confluence, culture medium exchanged with serum-free DMEM medium. CM were collected 2 days after change of media and stored at −20 °C until use. For serial experiments, cells were pretreated for 30 min with inhibitors, including Ly294002, Wortmannin, AKTi, U0126, PD98059, and HIF-1α inhibitor or transfected with miR-210 mimic, miR-210 inhibitor, ELK1 siRNA, p65 siRNA, and CTGF shRNA for 24 h, followed by treatment with CTGF for 24 h to prevent signaling via CTGF pathway.
EPCs migration assay
Migration activity was measured by Transwell assay (Corning, Costar, Tewksbury, MA, USA; pore size, 8-μm). About 1 × 104 EPCs were added to upper chamber in 200 μl of 10% FBS MV2 complete medium. Lower chamber contained 150 μl 20% FBS MV2 complete medium and 150 μl CM. Plates were incubated for 24 h at 37 °C in 5% CO2, cells fixed in 3.7% formaldehyde solution for 15 min and stained with 0.05% crystal violet in PBS for 15 min. Cells on upper side of filters were removed with cotton-tipped swabs, filters washed with PBS. Cells on undersides of filters were examined and counted under microscope. Each clone was plated in triplicate for each experiment, each experiment repeated at least three times.
Tube formation assay
Matrigel (BD Biosciences, Bedford, MA, USA) was dissolved overnight at 4 °C and 48-well plates prepared with 100 μl Matrigel in each well, after coating and incubating at 37 °C overnight. EPCs (3 × 104) were cultured in 200 μl media consisting of 50% EGM-MV2 medium and 50% CM. After 6 h incubation at 37 °C, tube formation was assessed with photomicroscope, each well photographed at × 200 magnification. Tube branches and total tube length were calculated using MacBiophotonics Image J software (Bethesda, MD, USA).
Fertilized chicken eggs were incubated at 38 °C with 80% humidity. Small window was made in shell on day 3 of chick embryo development under aseptic conditions, then resealed with adhesive tape. Eggs were returned to incubator until day 3 of chick embryo development. On day 7, CM from OASFs deposited in center of CAM. At 11 days, CAMs were collected for microscopy and photographic documentation, angiogenesis quantified by counting number of blood vessel branches; at least 10 viable embryos were tested for each treatment. All animal work conformed with protocol approved by the China Medical University (Taichung, Taiwan) Institutional Animal Care and Use Committees.
Matrigel plug assay
Matrigel plug angiogenesis was adapted from previously described assay.53 Four-week-old male nude mice were randomized as serum-free medium, OASFs/control-shRNA CM, or OASFs/CTGF-shRNA CM resuspended with Matrigel. Mice were subcutaneously injected with 300 μl of Matrigel. After 7 days, Matrigel pellets were harvested, partially fixed with 4% formalin, embedded in paraffin, then processed for immunohistochemistry staining for vessel marker CD31.
Data were presented as mean±standard error of the mean. Comparison between samples was performed by Student’s t-test; for more than two groups, we used one-way analysis of variance with Bonferroni’s post-hoc test. In all cases, P<0.05 was considered significant.
Connective tissue growth factor
OA synovial fibroblast
Nuclear factor kappa B
vascular endothelial growth factor
the small, non-coding microRNAs
glycerol-3-phosphate dehydrogenase 1-like
prolyl hydroxylases 2
small interfering RNA
endothelial progenitor cell
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This work was supported by grants from the Ministry of Science and Technology of Taiwan (MOST 103-2628-B-039-002-MY3).
The authors declare no conflict of interest.
Edited by M Agostini
Supplementary Information accompanies this paper on Cell Death and Disease website
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Liu, SC., Chuang, SM., Hsu, CJ. et al. CTGF increases vascular endothelial growth factor-dependent angiogenesis in human synovial fibroblasts by increasing miR-210 expression. Cell Death Dis 5, e1485 (2014). https://doi.org/10.1038/cddis.2014.453
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