衰老间充质干细胞:疾病机理与治疗策略

Current molecular biology reports Pub Date : 2020-12-01 Epub Date: 2020-10-28 DOI:10.1007/s40610-020-00141-0
Yajun Liu, Qian Chen
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引用次数: 0

摘要

综述目的:间充质干细胞(MSCs)已被广泛研究用于组织工程和再生医学的治疗。尽管间充质干细胞前景广阔,但最近的研究结果表明,间充质干细胞在修复过程中的复制可能会导致复制衰老和干细胞衰竭。在此,我们回顾了间充质干细胞衰老的基本机制、它如何导致退行性疾病,以及治疗这类疾病的潜在方法:新的证据显示,衰老的间充质干细胞与退行性疾病,尤其是与年龄相关的疾病,如骨关节炎和特发性肺纤维化之间存在联系。在这些疾病过程中,间充质干细胞会发生细胞衰老,并介导衰老相关分泌表型(SASP)来影响周围的微环境。因此,衰老间充质干细胞可通过增加衰老细胞数量和向邻近细胞扩散炎症来加速组织衰老。摘要:衰老间充质干细胞不仅会通过细胞衰老相关干细胞耗竭阻碍组织修复,还会通过启动和扩散衰老相关炎症介导组织变性。该研究提出了基于间充质干细胞的细胞疗法新策略,以去除、恢复或替代(3Rs)衰老的间充质干细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Senescent Mesenchymal Stem Cells: Disease Mechanism and Treatment Strategy.

Purpose of review: Mesenchymal stem cells (MSCs) have been extensively studied for therapeutic application in tissue engineering and regenerative medicine. Despite their promise, recent findings suggest that MSC replication during repair process may lead to replicative senescence and stem cell exhaustion. Here, we review the basic mechanisms of MSC senescence, how it leads to degenerative diseases, and potential treatments for such diseases.

Recent findings: Emerging evidence has shown a link between senescent MSCs and degenerative diseases, especially age-related diseases such as osteoarthritis and idiopathic pulmonary fibrosis. During these disease processes, MSCs undergo cell senescence and mediate Senescence Associated Secretory Phenotypes (SASP) to affect the surrounding microenvironment. Thus, senescent MSCs can accelerate tissue aging by increasing the number of senescent cells and spreading inflammation to neighboring cells.

Summary: Senescent MSCs not only hamper tissue repair through cell senescence associated stem cell exhaustion, but also mediate tissue degeneration by initiating and spreading senescence-associated inflammation. It suggests new strategies of MSC-based cell therapy to remove, rejuvenate, or replace (3Rs) the senescent MSCs.

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