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在小鼠骨关节炎模型中,关节内注射硫酸乙酰肝素6-O硫酸酯酶对软骨退变的抑制作用。

Suppression of cartilage degeneration by intra-articular injection of heparan sulfate 6-O endosulfatase in a mouse osteoarthritis model.

作者信息

Otsuki Shuhei, Murakami Tomohiko, Okamoto Yoshinori, Hoshiyama Yoshiaki, Oda Shuhei, Neo Masashi

机构信息

Department of Orthopedic Surgery, Osaka Medical College, Osaka, Japan.

出版信息

Histol Histopathol. 2017 Jul;32(7):725-733. doi: 10.14670/HH-11-838. Epub 2016 Nov 3.

DOI:10.14670/HH-11-838
PMID:27808352
Abstract

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.

摘要

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。

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