Department of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, China.
Department of Emergency, Renmin Hospital of Wuhan University, Wuhan, China.
J Cell Mol Med. 2021 Jan;25(1):120-131. doi: 10.1111/jcmm.15884. Epub 2020 Nov 17.
Osteoarthritis (OA) is an ageing-related disease characterized by articular cartilage degradation and joint inflammation. circRNA has been known to involve in the regulation of multiple inflammatory diseases including OA. However, the mechanism underlying how circRNA regulates OA remains to be elucidated. Here, we report circANKRD36 prevents OA chondrocyte apoptosis and inflammation by targeting miR-599, which specifically degrades Casz1. We performed circRNA sequencing in normal and OA tissues and found the expression of circANKRD36 is decreased in OA tissues. circANKRD36 is also reduced in IL-1β-treated human chondrocytes. FACS analysis and Western blot showed that the knockdown of circANKRD36 promotes the apoptosis and inflammation of chondrocytes in IL-1β stress. We then found miR-599 to be the target of circANKRD36 and correlate well with circANKRD36 both in vitro and in vivo. By database analysis and luciferase assay, Casz1 was found to be the direct target of miR-599. Casz1 helps to prevent apoptosis and inflammation of chondrocytes in response to IL-1β. In conclusion, our results proved circANKRD36 sponge miR-599 to up-regulate the expression of Casz1 and thus prevent apoptosis and inflammation in OA.
骨关节炎(OA)是一种与衰老相关的疾病,其特征为关节软骨降解和关节炎症。circRNA 已被证实参与多种炎症性疾病的调节,包括 OA。然而,circRNA 调节 OA 的机制仍有待阐明。在这里,我们报告 circANKRD36 通过靶向 miR-599 来防止 OA 软骨细胞凋亡和炎症,miR-599 特异性降解 Casz1。我们在正常和 OA 组织中进行了 circRNA 测序,发现 OA 组织中 circANKRD36 的表达降低。IL-1β 处理的人软骨细胞中 circANKRD36 的表达也降低。FACS 分析和 Western blot 显示,circANKRD36 的敲低促进了 IL-1β 应激下软骨细胞的凋亡和炎症。然后我们发现 miR-599 是 circANKRD36 的靶标,并且在体外和体内都与 circANKRD36 很好地相关。通过数据库分析和荧光素酶测定,发现 Casz1 是 miR-599 的直接靶标。Casz1 有助于防止软骨细胞对 IL-1β 的凋亡和炎症反应。总之,我们的结果证明 circANKRD36 通过海绵吸附 miR-599 来上调 Casz1 的表达,从而防止 OA 中的凋亡和炎症。