Otsuki Shuhei, Murakami Tomohiko, Okamoto Yoshinori, Hoshiyama Yoshiaki, Oda Shuhei, Neo Masashi
Department of Orthopedic Surgery, Osaka Medical College, Osaka, Japan.
Histol Histopathol. 2017 Jul;32(7):725-733. doi: 10.14670/HH-11-838. Epub 2016 Nov 3.
We previously reported that heparan sulfate 6-O endosulfatases (Sulfs) were expressed in articular cartilage, and that the Sulf-1 knockout mouse developed severe knee osteoarthritis. In this study, we hypothesised that intra-articular injection of Sulf-1 would prevent cartilage degeneration. After confirming that 1 mg/ml Sulf-1 did not induce ATDC5 cell death in vitro, gene expression of type II collagen and matrix metalloproteinase (MMP)-13 in the presence of Sulf-1 (1 100 ng/ml) were determined by quantitative real-time polymerase chain reaction. Sulf-1 was also injected intra-articularly into mice following surgical destabilisation of the medial meniscus to produce a model of osteoarthritis, and cartilage degeneration was evaluated by safranin O and MMP-13 staining. We also investigated fibroblast growth factor 2 (FGF2)/extracellular signal-regulated kinase (Erk) cell signalling by western blotting. Exposure to Sulf-1 in vitro increased type II collagen expression and decreased MMP-13 expression in a concentration-dependent manner. Sulf-1 injection into the mouse osteoarthritic knee significantly suppressed glycosaminoglycan loss and MMP-13 expression. Erk1/2 signalling pathway activation was significantly reduced by Sulf-1 and FGF2. These findings indicate that Sulf-1 prevents cartilage degeneration by suppressing MMP-13 via an effect on FGF2/Erk1/2 signalling.
我们之前报道过硫酸乙酰肝素6 - O - 硫酸酯酶(Sulfs)在关节软骨中表达,并且Sulf - 1基因敲除小鼠会发展为严重的膝关节骨关节炎。在本研究中,我们假设关节腔内注射Sulf - 1可预防软骨退变。在确认1 mg/ml的Sulf - 1在体外不会诱导ATDC5细胞死亡后,通过定量实时聚合酶链反应测定在存在Sulf - 1(1 - 100 ng/ml)的情况下II型胶原蛋白和基质金属蛋白酶(MMP)- 13的基因表达。在手术造成内侧半月板不稳定以建立骨关节炎模型后,也将Sulf - 1关节腔内注射到小鼠体内,通过番红O和MMP - 13染色评估软骨退变情况。我们还通过蛋白质印迹法研究了成纤维细胞生长因子2(FGF2)/细胞外信号调节激酶(Erk)细胞信号传导。体外暴露于Sulf - 1以浓度依赖的方式增加II型胶原蛋白表达并降低MMP - 13表达。向小鼠骨关节炎膝关节内注射Sulf - 1可显著抑制糖胺聚糖丢失和MMP - 13表达。Sulf - 1和FGF2可显著降低Erk1/2信号通路的激活。这些发现表明,Sulf - 1通过影响FGF2/Erk1/2信号传导抑制MMP - 13,从而预防软骨退变。