Department of Orthopaedic Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, Japan.
J Orthop Res. 2012 Nov;30(11):1738-45. doi: 10.1002/jor.22142. Epub 2012 May 10.
The intrinsic zone-specific properties of the menisci are determined by biomechanical environments. In this study, we examined mechanical stretch-dependent expression of multifunctional growth factor CYR61/CTGF/NOV (CCN) 2, and investigated the role of CCN2 in meniscus cells. Uni-axial cyclic tensile strain (CTS) was applied using a STB-140 system. CTS-induced expression of CCN2 and α1(I) collagen (COL1A1) was assessed by quantitative real-time PCR analysis. The distribution of CCN2 and Smad2/3 in stretched cells was investigated by immunohistochemical analysis. Smad2/3-dependent CCN2 transactivation was measured by luciferase reporter assay. The relationship between Smad2/3 and CTS-induced CCN2 transcription was investigated by chromatin immunoprecipitation. CTS stimulated gene expression of CCN2 and COL1A1 in inner meniscus cells, but not in outer meniscus cells. Recombinant CCN2 increased COL1A1 expression only in inner meniscus cells. CCN2 synthesis and nuclear translocalization of phosphorylated Smad2/3 in inner meniscus cells were stimulated by CTS. The CCN2 promoter activity was synergistically enhanced by overexpressed Smad3 in stretched inner meniscus cells, but was not by Smad2. Chromatin immunoprecipitation revealed that CTS increased the association between Smad3 and the Smad-binding element on the CCN2 proximal promoter in inner meniscus cells. Our results suggest that stretch-induced CCN2 may have a crucial role in regulating COL1A1 expression in the inner meniscus.
半月板的内在区域特异性特性由生物力学环境决定。在本研究中,我们研究了机械拉伸依赖性多功能生长因子 CYR61/CTGF/NOV(CCN)2 的表达,并研究了 CCN2 在半月板细胞中的作用。使用 STB-140 系统施加单轴循环拉伸应变(CTS)。通过定量实时 PCR 分析评估 CTS 诱导的 CCN2 和 α1(I)胶原(COL1A1)表达。通过免疫组织化学分析研究拉伸细胞中 CCN2 和 Smad2/3 的分布。通过荧光素酶报告基因测定测量 Smad2/3 依赖性 CCN2 转激活。通过染色质免疫沉淀研究 Smad2/3 和 CTS 诱导的 CCN2 转录之间的关系。CTS 刺激内半月板细胞中 CCN2 和 COL1A1 的基因表达,但不刺激外半月板细胞。重组 CCN2 仅在内半月板细胞中增加 COL1A1 表达。CTS 刺激内半月板细胞中 CCN2 合成和磷酸化 Smad2/3 的核易位。在拉伸的内半月板细胞中,过表达的 Smad3 协同增强了 CCN2 启动子活性,但 Smad2 则不然。染色质免疫沉淀显示 CTS 增加了 Smad3 与内半月板细胞中 CCN2 近端启动子上的 Smad 结合元件之间的关联。我们的结果表明,拉伸诱导的 CCN2 可能在内半月板中调节 COL1A1 表达中起关键作用。