...
首页> 外文期刊>Progress in Artificial Intelligence >Neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis
【24h】

Neural cell adhesion molecule regulates chondrocyte hypertrophy in chondrogenic differentiation and experimental osteoarthritis

机译:神经细胞粘附分子调节软骨内分化和实验性骨关节炎的软骨细胞肥大

获取原文
获取原文并翻译 | 示例
           

摘要

Chondrocyte hypertrophy-like change is an important pathological process of osteoarthritis (OA), but the mechanism remains largely unknown. Neural cell adhesion molecule (NCAM) is highly expressed and involved in the chondrocyte differentiation of mesenchymal stem cells (MSCs). In this study, we found that NCAM deficiency accelerates chondrocyte hypertrophy in articular cartilage and growth plate of OA mice. NCAM deficiency leads to hypertrophic chondrocyte differentiation in both murine MSCs and chondrogenic cells, in which extracellular signal-regulated kinase (ERK) signaling plays an important role. Moreover, NCAM expression is downregulated in an interleukin-1 beta-stimulated OA cellular model and monosodium iodoacetate-induced OA rats. Overexpression of NCAM substantially inhibits hypertrophic differentiation in the OA cellular model. In conclusion, NCAM could inhibit hypertrophic chondrocyte differentiation of MSCs by inhibiting ERK signaling and reduce chondrocyte hypertrophy in experimental OA model, suggesting the potential utility of NCAM as a novel therapeutic target for alleviating chondrocyte hypertrophy of OA.
机译:软骨细胞肥大样变化是骨关节炎(OA)的重要病理过程,但该机制仍然很大程度上未知。神经细胞粘附分子(NCAM)高度表达并参与间充质干细胞(MSCs)的软骨细胞分化。在这项研究中,我们发现NCAM缺陷在OA小鼠的关节软骨和生长板中加速了软骨细胞肥大。 NCAM缺乏导致鼠MSCs和软骨内细胞中的肥厚性软骨细胞分化,其中细胞外信号调节激酶(ERK)信号传导起着重要作用。此外,NCAM表达在白细胞介素-1β刺激的OA细胞模型和单钠碘酸钠诱导的OA大鼠中下调。 NCAM的过表达基本上抑制OA蜂窝模型中的肥厚分化。总之,NCAM通过抑制ERK信号传导和减少实验性OA模型中的软骨细胞肥大来抑制MSCs的肥厚性软骨细胞分化,表明NCAM作为减轻OA软骨细胞肥大的新型治疗靶标的潜在效用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号