软骨细胞
生物
软骨
细胞生物学
细胞凋亡
骨关节炎
细胞外基质
癌症研究
信号转导
生物化学
病理
医学
解剖
替代医学
作者
Jie Yuan,Jingyuan Tian,Ruxing Liu,Xiangyun Qiu,Dongmei He,Guanghui He,Tao Zhang,Pengcui Li,Bin Zhao,Yongfeng Wang
摘要
ABSTRACT This study investigates the role and mechanism of Coactivator Associated Arginine Methyltransferase 1 (CARM1) in osteoarthritis (OA). OA is a prevalent joint disease characterized by cartilage degradation, subchondral bone remodeling, and inflammation. Our research revealed that CARM1 expression is significantly increased in the cartilage tissues of OA patients and OA model mice. Experimental results showed that inhibiting CARM1 reduces cartilage matrix degradation and chondrocyte apoptosis, while overexpression of CARM1 exacerbates these conditions. Mechanistically, CARM1 regulates OA progression through the phosphorylation of the ERK1/2 signaling pathway. Inhibition of CARM1 suppresses ERK1/2 activation, thereby reducing extracellular matrix degradation and chondrocyte apoptosis. These findings suggest that the CARM1‐ERK1/2 axis is crucial in modulating cartilage matrix metabolism and chondrocyte apoptosis in OA, highlighting CARM1 as a potential therapeutic target for OA treatment.
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