Connexins43 expression and its effect on chondrogenesis in the cocultures of articular chondrocytes with bone marrow mesenchymal stromal cells

Zhao Wenhui, L. Hui, Zhang Shaogong, Wu Chun-jiang, Z. Ming, Zhu Xia, Feng Wanwen
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Abstract

Objective To investigate connexins43 (Cx43) expression and its effect on chondrogenesis in the cocultures of bone marrow mesenchymal stromal cells (BMSCs)with articular chondrocytes (ACs). Methods The second passage BMSCs and ACs from New Zealand white rabbits were cocultured at the ratio of 3∶1 (BMSCs to ACs) for 21 days in vitro. The coculture patterns included the cell-cell contact coculture in the 24-well plates as experimental group and the cell-cell noncontact coculture through a Transwell chamber as control group. Cx43 inhibitor 18-ɑ glycyrrhetnic acid (GA) 50 μmol/L was supplemented in each group and subsequently cocultured for 21 days. Levels of glycosaminoglycans (GAG) in the medium supernatants of each group were detected by enzyme linked immunosorbent assay (ELISA). Expression of Cx43 and type Ⅱ collagen a1 (COL2a1) in the each group were analyzed using immunocytochemistry staining (ICC) and Western blotting. Results GAG levels of the medium supernatants, expression of Cx43 and COL2a1 were significantly high in the experimental group compared with control group [(327.517±24.612) ng/L vs. (171.612±13.163) ng/L, t=13.683, P 0.05; 0.240±0.028 vs. 0.223±0.026, t=1.086, P>0.05], whereas these all decreased significantly (t=17.541, 6.015, P 0.05). Conclusion Expression of Cx43 increases and Cx43 promotes chondrogenesis in contact coculture of BMSCs with ACs, which plays a major role in the regulation of chondrogenic differentiation. Key words: Bone marrow mesenchymal stem cell; Chondrocyte; Coculture; Connexins 43; Chondrogenesis
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关节软骨细胞与骨髓间充质间质细胞共培养中Connexins43的表达及其对软骨形成的影响
目的探讨骨髓间充质基质细胞(BMSCs)与关节软骨细胞(ACs)共培养时连接蛋白43 (connexins43, Cx43)的表达及其对软骨形成的影响。方法将新西兰大白兔二代骨髓间充质干细胞与ACs按3∶1的比例体外共培养21 d。共培养模式包括24孔板细胞-细胞接触共培养作为实验组和Transwell腔细胞-细胞非接触共培养作为对照组。每组添加Cx43抑制剂18- α甘草酸(GA) 50 μmol/L,共培养21 d。采用酶联免疫吸附法(ELISA)检测各组培养基上清液中糖胺聚糖(GAG)水平。免疫细胞化学染色(ICC)和Western blotting分析各组Cx43和Ⅱ型胶原a1 (COL2a1)的表达。结果实验组培养液上清液GAG水平、Cx43、COL2a1表达均显著高于对照组[(327.517±24.612)ng/L vs(171.612±13.163)ng/L, t=13.683, P 0.05;分别为0.240±0.028比0.223±0.026,t=1.086, P < 0.05],而两者均显著降低(t=17.541, 6.015, P < 0.05)。结论在骨髓间充质干细胞与ACs接触共培养过程中,Cx43表达增加,Cx43促进软骨形成,在软骨分化调控中起重要作用。关键词:骨髓间充质干细胞;软骨细胞;Coculture;连接素43;软骨形成
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