自噬与细胞重编程。
Autophagy and cell reprogramming.
作者信息
Wang Shuo, Xia Pengyan, Rehm Markus, Fan Zusen
机构信息
CAS Key Laboratory of Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
出版信息
Cell Mol Life Sci. 2015 May;72(9):1699-713. doi: 10.1007/s00018-014-1829-3. Epub 2015 Jan 9.
Autophagy is an evolutionarily conserved process that degrades cytoplasmic components, thus contributing to cell survival and tissue homeostasis. Recent studies have demonstrated that autophagy maintains stem cells in relatively undifferentiated states (stemness) and also contributes to differentiation processes. Autophagy likewise plays a crucial role in somatic cell reprogramming, a finely regulated process that resets differentiated cells to a pluripotent state and that requires comprehensive alterations in transcriptional activities and epigenetic signatures. Autophagy assists in manifesting the functional consequences that arise from these alterations by modifying cellular protein expression profiles. The role of autophagy appears to be particularly relevant for early phases of cell reprogramming during the generation of induced pluripotent stems cells (iPSCs). In this review, we provide an overview of the core molecular machinery that constitutes the autophagic degradation system, describe the roles of autophagy in maintenance, self-renewal, and differentiation of stem cells, and discuss the autophagic process and its regulation during cell reprogramming.
自噬是一个进化上保守的过程,它降解细胞质成分,从而有助于细胞存活和组织稳态。最近的研究表明,自噬使干细胞维持在相对未分化的状态(干性),并且也有助于分化过程。自噬同样在体细胞重编程中起关键作用,体细胞重编程是一个精细调控的过程,它将分化细胞重置为多能状态,并且需要转录活性和表观遗传特征的全面改变。自噬通过修饰细胞蛋白质表达谱来协助展现这些改变所产生的功能后果。自噬的作用似乎在诱导多能干细胞(iPSC)产生过程中的细胞重编程早期阶段尤为重要。在这篇综述中,我们概述了构成自噬降解系统的核心分子机制,描述了自噬在干细胞维持、自我更新和分化中的作用,并讨论了细胞重编程过程中的自噬过程及其调控。