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外在因素影响干细胞抗衰老的分子机制。

Molecular mechanism of extrinsic factors affecting anti-aging of stem cells.

机构信息

Tzyy Yue Wong, Mairim Alexandra Solis, Ying-Hui Chen, Lynn Ling-Huei Huang, Institute of Biotechnology, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan 70101, Taiwan.

出版信息

World J Stem Cells. 2015 Mar 26;7(2):512-20. doi: 10.4252/wjsc.v7.i2.512.

Abstract

Scientific evidence suggests that stem cells possess the anti-aging ability to self-renew and maintain differentiation potentials, and quiescent state. The objective of this review is to discuss the micro-environment where stem cells reside in vivo, the secreted factors to which stem cells are exposed, the hypoxic environment, and intracellular factors including genome stability, mitochondria integrity, epigenetic regulators, calorie restrictions, nutrients, and vitamin D. Secreted tumor growth factor-β and fibroblast growth factor-2 are reported to play a role in stem cell quiescence. Extracellular matrices may interact with caveolin-1, the lipid raft on cell membrane to regulate quiescence. N-cadherin, the adhesive protein on niche cells provides support for stem cells. The hypoxic micro-environment turns on hypoxia-inducible factor-1 to prevent mesenchymal stem cells aging through p16 and p21 down-regulation. Mitochondria express glucosephosphate isomerase to undergo glycolysis and prevent cellular aging. Epigenetic regulators such as p300, protein inhibitors of activated Stats and H19 help maintain stem cell quiescence. In addition, calorie restriction may lead to secretion of paracrines cyclic ADP-ribose by intestinal niche cells, which help maintain intestinal stem cells. In conclusion, it is crucial to understand the anti-aging phenomena of stem cells at the molecular level so that the key to solving the aging mystery may be unlocked.

摘要

科学证据表明,干细胞具有自我更新和维持分化潜能的抗衰老能力,并处于静止状态。本综述的目的是讨论干细胞在体内所处的微环境、干细胞暴露于其中的分泌因子、缺氧环境以及包括基因组稳定性、线粒体完整性、表观遗传调节剂、热量限制、营养物质和维生素 D 在内的细胞内因素。据报道,分泌的肿瘤生长因子-β和成纤维细胞生长因子-2在干细胞静止中发挥作用。细胞外基质可能与细胞膜上的脂筏 caveolin-1 相互作用,以调节静止。位于龛细胞上的黏附蛋白 N-钙黏蛋白为干细胞提供支持。缺氧微环境会激活缺氧诱导因子-1,通过下调 p16 和 p21 来防止间充质干细胞衰老。线粒体表达葡萄糖磷酸异构酶以进行糖酵解并防止细胞衰老。表观遗传调节剂,如 p300、激活 Stats 的蛋白抑制剂和 H19,有助于维持干细胞静止。此外,热量限制可能导致肠道龛细胞分泌旁分泌环 ADP-核糖,从而有助于维持肠道干细胞。总之,从分子水平理解干细胞的抗衰老现象至关重要,这样,解开衰老之谜的关键或许就能被解开。

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