Department of Orthopaedic Surgery, Mie University Graduate School of Medicine, 2-174, Edobashi, Tsu-city, Mie 514-8507, Japan.
Biochem Biophys Res Commun. 2010 Oct 1;400(4):493-9. doi: 10.1016/j.bbrc.2010.08.070. Epub 2010 Aug 22.
The aggregation of chondroprogenitor mesenchymal cells into precartilage condensation represents one of the earliest events in chondrogenesis. N-cadherin is a key cell adhesion molecule implicated in chondrogenic differentiation. Recently, ADAM10-mediated cleavage of N-cadherin has been reported to play an important role in cell adhesion, migration, development and signaling. However, the significance of N-cadherin cleavage in chondrocyte differentiation has not been determined. In the present study, we found that the protein turnover of N-cadherin is accelerated during the early phase of chondrogenic differentiation in ATDC5 cells. Therefore, we generated the subclones of ATDC5 cells overexpressing wild-type N-cadherin, and two types of subclones overexpressing a cleavage-defective N-cadherin mutant, and examined the response of these cells to insulin stimulation. The ATDC5 cells overexpressing cleavage-defective mutants severely prevented the formation of cartilage aggregates, proteoglycan production and the induction of chondrocyte marker gene expression, such as type II collagen, aggrecan and type X collagen. These results suggested that the cleavage of N-cadherin is essential for chondrocyte differentiation.
软骨祖细胞间的聚集形成软骨前体凝聚是软骨发生的最早事件之一。N-钙黏蛋白是一种关键的细胞黏附分子,与软骨分化有关。最近,ADAM10 介导的 N-钙黏蛋白的切割被报道在细胞黏附、迁移、发育和信号转导中发挥重要作用。然而,N-钙黏蛋白切割在软骨细胞分化中的意义尚未确定。在本研究中,我们发现 N-钙黏蛋白的蛋白周转在 ATDC5 细胞的软骨分化早期阶段加速。因此,我们生成了过表达野生型 N-钙黏蛋白的 ATDC5 细胞亚克隆,以及过表达两种类型的切割缺陷型 N-钙黏蛋白突变体的亚克隆,并检测了这些细胞对胰岛素刺激的反应。过表达切割缺陷型突变体的 ATDC5 细胞严重阻止了软骨聚集体的形成、蛋白聚糖的产生以及软骨细胞标记基因(如 II 型胶原、聚集蛋白聚糖和 X 型胶原)的诱导表达。这些结果表明 N-钙黏蛋白的切割对于软骨细胞分化是必要的。