Department of Orthopedics, Peking Union Medical College Hospital, No. 1, Shuaifuyuan, Wangfujing Street, Dongcheng District, Beijing, 100730, People's Republic of China.
Chinese Academy of Medical Sciences & Peking Union Medical College, No. 9, Dongdan Santiao, Dongcheng District, Beijing, 100730, People's Republic of China.
Inflammopharmacology. 2022 Jun;30(3):843-853. doi: 10.1007/s10787-022-00923-1. Epub 2022 Apr 19.
The changed biomechanical environment of chondrocytes elicited by altered extracellular matrix is reported to accelerate the progression of OA. MicroRNAs (miRNAs or miRs) have emerged as major regulators in chondrocyte function. Hence, we explored effect of miR-23a/b-3p on OA in regulating chondrocyte growth. The medial meniscus and anterior cruciate ligaments of right knee was removed to induce a mouse model of OA. miR-23a/b-3p and Gremlin1 (Grem1) expressions in OA were determined by RT-qPCR. Dual luciferase reporter gene assay was conducted to assess their relationship in the context of OA. Loss- and gain-of-function assays were adopted to clarify their effects on OA by determining the release of pro-inflammatory proteins and the apoptosis of chondrocytes. RT-qPCR determined increased miR-23a/b-3p expression and decreased Grem1 expression in the setting OA. Inhibiting miR-23a/b-3p or overexpressing Grem1 activated transforming growth factor-β/solvated metal atom dispersed 3 (TGF-β/Smad) signaling to prevent OA development. Silencing Grem1 ablated suppressive effects of miR-23a/b-3p inhibitor on the release of pro-inflammatory proteins and the apoptosis of chondrocytes. To conclude, inhibition of miR-23a/b-3p delays OA progression through Grem1-mediated activation of TGF-β/Smad signaling, contributing to deepen understanding of the pathogenesis of OA.
细胞外基质改变引起的软骨细胞生物力学环境的改变被报道会加速 OA 的进展。 microRNAs(miRNAs 或 miRs)已成为软骨细胞功能的主要调节因子。因此,我们探讨了 miR-23a/b-3p 对调节软骨细胞生长的 OA 的影响。通过切除右膝内侧半月板和前交叉韧带来诱导 OA 小鼠模型。通过 RT-qPCR 确定 OA 中 miR-23a/b-3p 和 Gremlin1(Grem1)的表达。双荧光素酶报告基因检测评估它们在 OA 背景下的关系。通过测定促炎蛋白的释放和软骨细胞的凋亡,采用缺失和获得功能测定来阐明它们对 OA 的影响。RT-qPCR 确定 OA 中 miR-23a/b-3p 表达增加,Grem1 表达降低。抑制 miR-23a/b-3p 或过表达 Grem1 激活转化生长因子-β/溶解金属原子分散 3(TGF-β/Smad)信号通路,以防止 OA 发展。沉默 Grem1 消除了 miR-23a/b-3p 抑制剂对促炎蛋白释放和软骨细胞凋亡的抑制作用。总之,抑制 miR-23a/b-3p 通过 Grem1 介导的 TGF-β/Smad 信号通路激活延迟 OA 进展,有助于加深对 OA 发病机制的理解。