Wang Ruoxi, Wang Yu, Zhu Lisha, Liu Yan, Li Weiran
Laboratory of Biomimetic Nanomaterials, Department of Orthodontics, Peking University School and Hospital of Stomatology, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, Beijing 100081, China.
Stem Cells Int. 2020 Sep 10;2020:8836258. doi: 10.1155/2020/8836258. eCollection 2020.
Mesenchymal stem cells (MSCs) are a reliable source for cell-based regenerative medicine owing to their multipotency and biological functions. However, aging-induced systemic homeostasis disorders and cell culture passaging induce a functional decline of MSCs, switching MSCs to a senescent status with impaired self-renewal capacity and biased differentiation tendency. MSC functional decline accounts for the pathogenesis of many diseases and, more importantly, limits the large-scale applications of MSCs in regenerative medicine. Growing evidence implies that epigenetic mechanisms are a critical regulator of the differentiation programs for cell fate and are subject to changes during aging. Thus, we here review epigenetic dysregulations that contribute to MSC aging and osteoporosis. Comprehending detailed epigenetic mechanisms could provide us with a novel horizon for dissecting MSC-related pathogenesis and further optimizing MSC-mediated regenerative therapies.
间充质干细胞(MSCs)因其多能性和生物学功能,是基于细胞的再生医学的可靠细胞来源。然而,衰老引起的全身稳态紊乱和细胞培养传代导致MSCs功能衰退,使其转变为衰老状态,自我更新能力受损且分化倾向出现偏差。MSCs功能衰退是许多疾病发病机制的原因,更重要的是,限制了MSCs在再生医学中的大规模应用。越来越多的证据表明,表观遗传机制是细胞命运分化程序的关键调节因子,并且在衰老过程中会发生变化。因此,我们在此综述导致MSCs衰老和骨质疏松的表观遗传失调。了解详细的表观遗传机制可以为剖析与MSCs相关的发病机制以及进一步优化MSCs介导的再生疗法提供新的视角。