Department of Orthopedics, The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi 214000, Jiangsu Province, China.
Biomed Res Int. 2019 May 8;2019:1484152. doi: 10.1155/2019/1484152. eCollection 2019.
Osteoarthritis (OA) is a chronic joint disease characterized by articular cartilage regression. The etiology of OA is diverse, the exact pathogenesis of which remains unclear. Autophagy is a conserved maintenance mechanism in eukaryotic cells. Dysfunction of chondrocyte autophagy is regarded as a crucial pathogenesis of cartilage degradation in OA. MircoRNAs (miRNAs) are a category of small noncoding RNAs, acting as posttranscriptional modulators that regulate biological processes and cell signaling pathways via target genes. A series of miRNAs are involved in the progression of chondrocyte autophagy and are connected with numerous factors and pathways. This article focuses on the mechanisms of chondrocyte autophagy in OA and reviews the role of miRNA in their modulation. Potentially relevant miRNAs are also discussed in order to provide new directions for future research and improve our understanding of the autophagic network of miRNAs.
骨关节炎(OA)是一种以关节软骨退行性变为特征的慢性关节疾病。OA 的病因多种多样,其确切发病机制尚不清楚。自噬是真核细胞中一种保守的维持机制。软骨细胞自噬功能障碍被认为是 OA 中软骨降解的关键发病机制。微小 RNA(miRNA)是一类小的非编码 RNA,作为转录后调节因子,通过靶基因调节生物过程和细胞信号通路。一系列 miRNA 参与了软骨细胞自噬的进展,并与许多因素和途径有关。本文主要关注 OA 中软骨细胞自噬的机制,并综述了 miRNA 在其调节中的作用。还讨论了潜在相关的 miRNA,以期为未来的研究提供新的方向,并加深对 miRNA 自噬网络的理解。