Differentiation of adult mesenchymal stem cells into chondrogenic cells using small molecules or microRNA

Onju Ham, C. Lee, Ran Kim, J. Lee, Min Young Lee, Jongmin Kim, K. Hwang, Woochul Chang
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引用次数: 1

Abstract

Transplantation of mesenchymal stem cells (MSCs) into osteoarthritis (OA) and rheumatoid arthritis (RA) patients has been studied as a therapeutic tool for regeneration of damaged cartilage. MSCs have several beneficial effects, including immunomodulatory activity, and release various paracrine factors. Despite their abundant beneficial effects, transplantation of naive MSCs is hampered by heterogeneous populations of differentiated and undifferentiated stem cells. However, transplantation of differentiated MSCs overcomes the problem of transplantation of naive MSCs. Thus, to repair damaged tissue, a therapeutic strategy based on the use of differentiated MSCs is needed to treat RA or OA patients. Here, we summarize methods that can regulate differentiation of MSCs into chondrocytes by small molecules or miRNAs, and suggest the capacity of patient tissue-derived MSCs as a therapeutic strategy for treatment of OA or RA patients.
利用小分子或microRNA将成体间充质干细胞分化为软骨细胞
骨关节炎(OA)和类风湿关节炎(RA)患者间充质干细胞(MSCs)移植作为损伤软骨再生的治疗工具已被研究。间充质干细胞具有多种有益作用,包括免疫调节活性,并释放多种旁分泌因子。尽管MSCs具有丰富的有益作用,但其移植受到分化和未分化干细胞异质群体的阻碍。然而,分化的间充质干细胞移植克服了幼稚间充质干细胞移植的难题。因此,为了修复受损组织,需要一种基于使用分化MSCs的治疗策略来治疗RA或OA患者。在这里,我们总结了通过小分子或mirna调节MSCs向软骨细胞分化的方法,并提出了患者组织来源的MSCs作为治疗OA或RA患者的治疗策略的能力。
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