Saint Petersburg Institute of Bioregulation and Gerontology, Dynamo pr. 3, 197110 Saint Petersburg, Russia.
Pavlov Institute of Physiology of Russia Academy of Sciences, Makarova emb. 6, 199034 Saint Petersburg, Russia.
Int J Mol Sci. 2023 May 8;24(9):8415. doi: 10.3390/ijms24098415.
The search for innovative ways to treat osteoarthritis (OA) is an urgent task for molecular medicine and biogerontology. OA leads to disability in persons of middle and older age, while safe and effective methods of treating OA have not yet been discovered. The directed differentiation of mesenchymal stem cells (MSCs) into chondrocytes is considered one of the possible methods to treat OA. This review describes the main molecules involved in the chondrogenic differentiation of MSCs. The peptides synthesized on the basis of growth factors' structures (SK2.1, BMP, B2A, and SSPEPS) and components of the extracellular matrix of cartilage tissue (LPP, CFOGER, CMP, RDG, and N-cadherin mimetic peptide) offer the greatest promise for the regulation of the chondrogenic differentiation of MSCs. These peptides regulate the WNT, ERK-p38, and Smad 1/5/8 signaling pathways, gene expression, and the synthesis of chondrogenic differentiation proteins such as COL2, SOX9, ACAN, etc.
寻找治疗骨关节炎(OA)的创新方法是分子医学和生物老年学的紧迫任务。OA 导致中年和老年人残疾,而尚未发现治疗 OA 的安全有效方法。间充质干细胞(MSCs)向软骨细胞的定向分化被认为是治疗 OA 的一种可能方法。本综述描述了参与 MSC 软骨分化的主要分子。基于生长因子结构(SK2.1、BMP、B2A 和 SSPEPS)和软骨组织细胞外基质成分(LPP、CFOGER、CMP、RDG 和 N-钙黏蛋白模拟肽)合成的肽在调节 MSC 的软骨分化方面具有最大的应用前景。这些肽调节 WNT、ERK-p38 和 Smad 1/5/8 信号通路、基因表达以及 COL2、SOX9、ACAN 等软骨分化蛋白的合成。