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基于间充质干细胞的软骨再生方法与细胞衰老:我们能否操纵细胞衰老和功能?

Mesenchymal Stem Cell-Based Cartilage Regeneration Approach and Cell Senescence: Can We Manipulate Cell Aging and Function?

机构信息

1 Human Anatomy and Histology Section, Department of Biomedical and Biotechnological Sciences, School of Medicine, University of Catania , Catania, Italy .

2 Musculoskeletal Regeneration, AO Research Institute Davos , Davos Platz, Switzerland .

出版信息

Tissue Eng Part B Rev. 2017 Dec;23(6):529-539. doi: 10.1089/ten.TEB.2017.0083. Epub 2017 Jun 22.

Abstract

Aging is the most prominent risk factor triggering several degenerative diseases, such as osteoarthritis (OA). Due to its poor self-healing capacity, once injured cartilage needs to be reestablished. This process might be approached through resorting to cell-based therapies and/or tissue engineering. Human mesenchymal stem cells (MSCs) represent a promising approach due to their chondrogenic differentiation potential. Presently, in vitro chondrogenic differentiation of MSCs is limited by two main reasons as follows: aging of MSCs, which determines the loss of cell proliferative and differentiation capacity and MSC-derived chondrocyte hypertrophic differentiation, which limits the use of these cells in cartilage tissue regeneration approach. The effect of aging on MSCs is fundamental for stem cell-based therapy development, especially in older subjects. In the present review we focus on homeostasis alterations occurring in MSC-derived chondrocytes during in vitro aging. Moreover, we deal with potential cell aging regulation approaches, such as cell stimulation through telomerase activators, mechanical strain, and epigenetic regulation. Future investigations in this field might provide new insights into innovative strategies for cartilage regeneration and potentially inspire novel therapeutic approaches for OA treatment.

摘要

衰老是引发多种退行性疾病的最显著风险因素,如骨关节炎(OA)。由于其自我修复能力差,一旦软骨受伤就需要重建。这一过程可以通过细胞疗法和/或组织工程来实现。由于具有成软骨分化潜力,人类间充质干细胞(MSCs)是一种很有前途的方法。目前,由于以下两个主要原因,MSCs 的体外软骨分化受到限制:MSCs 的衰老,决定了细胞增殖和分化能力的丧失,以及 MSC 来源的软骨细胞肥大分化,这限制了这些细胞在软骨组织再生方法中的应用。衰老对 MSCs 的影响是基于干细胞的治疗发展的基础,特别是在老年人群中。在本综述中,我们重点关注 MSC 来源的软骨细胞在体外衰老过程中发生的动态平衡改变。此外,我们还探讨了潜在的细胞衰老调控方法,如端粒酶激活剂、机械应变和表观遗传调控对细胞的刺激。该领域的未来研究可能为软骨再生的创新策略提供新的见解,并可能为 OA 的治疗提供新的治疗方法。

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