Deng RuLin, Zhang HongJun, Huang Lei, Xiong Xin, Fu Xiaoling
Department of Orthopedics, Nanchang HongDu Hospital of Traditional Chinese Medicine, NanChang, Jiangxi 330006, China.
Department of Orthopedics, Jiangxi provincial People's Hospital Affiliated to Nanchang University, NanChang, Jiangxi 330006, China.
Saudi J Biol Sci. 2021 Aug;28(8):4270-4275. doi: 10.1016/j.sjbs.2021.06.091. Epub 2021 Jul 3.
Knee osteoarthritis (KOA) is a chronic joint disorder involving the articular cartilage and tissues around the synovial joint. The key objective of this study was to determine the effect of miR-186-5p administration on the expression of pathogenic signalling in the chondrocytes using a surgical destabilization of the medial meniscus (DMM) model of KOA, and to testify the mechanism of P2X7-mediated regulation of RUNX2/ADAMTS5 axis by miR-186 in the KOA rats. After eight weeks of intra-articular injection of the miR-186-5p and negative control lentivirus samples, the knee cartilage tissues were subjected to histopathological analysis Safranin-O/Fast green staining. Further, the articular chondrocytes were separated and analysed for various proteins including P2X7, cathepsin-K, RUNX2 and ADAMTS5 using Western blotting method. We observed that the protein expressions of P2X7, cathepsin-K/RUNX2/ADAMTS5, and also MMP-13 were upmodulated in the KOA rats, while intra-articular miR-186-5p lentivirus administration prevented these aberrations. Hence, the study concludes that miR-186 orchestrates P2X7 expression and the P2X7-mediated cathepsin-K/RUNX2/ADAMTS5 axis and regulates the pathogenesis of KOA. In light of this evidence, we propose that molecular therapeutic interventions targeting miR-186 activation might attenuate osteoarthritic cartilage degeneration.
膝骨关节炎(KOA)是一种涉及关节软骨和滑膜关节周围组织的慢性关节疾病。本研究的主要目的是利用KOA的内侧半月板手术失稳(DMM)模型,确定给予miR-186-5p对软骨细胞中致病信号表达的影响,并验证miR-186在KOA大鼠中对P2X7介导的RUNX2/ADAMTS5轴的调控机制。在关节内注射miR-186-5p和阴性对照慢病毒样本八周后,对膝关节软骨组织进行番红O/固绿染色的组织病理学分析。此外,分离关节软骨细胞,采用蛋白质印迹法分析包括P2X7、组织蛋白酶K、RUNX2和ADAMTS5在内的各种蛋白质。我们观察到,KOA大鼠中P2X7、组织蛋白酶K/RUNX2/ADAMTS5以及MMP-13的蛋白表达上调,而关节内给予miR-186-5p慢病毒可防止这些异常。因此,该研究得出结论,miR-186协调P2X7表达以及P2X7介导的组织蛋白酶K/RUNX2/ADAMTS5轴,并调节KOA的发病机制。鉴于这一证据,我们提出针对miR-186激活的分子治疗干预可能会减轻骨关节炎软骨退变。