Epigenetic perturbations in aging stem cells.

Sara Russo Krauss, Gerald de Haan
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引用次数: 7

Abstract

Stem cells maintain homeostasis in all regenerating tissues during the lifespan of an organism. Thus, age-related functional decline of such tissues is likely to be at least partially explained by molecular events occurring in the stem cell compartment. Some of these events involve epigenetic changes, which may dictate how an aging genome can lead to differential gene expression programs. Recent technological advances have made it now possible to assess the genome-wide distribution of an ever-increasing number of epigenetic marks. As a result, the hypothesis that there may be a causal role for an altered epigenome contributing to the functional decline of cells, tissues, and organs in aging organisms can now be explored. In this paper, we review recent developments in the field of epigenetic regulation of stem cells, and how this may contribute to aging.

Abstract Image

衰老干细胞的表观遗传扰动。
在生物体的生命周期中,干细胞在所有再生组织中维持稳态。因此,这些组织与年龄相关的功能衰退可能至少部分地由干细胞室中发生的分子事件来解释。其中一些事件涉及表观遗传变化,这可能决定了衰老的基因组如何导致不同的基因表达程序。最近的技术进步使得现在有可能评估越来越多的表观遗传标记的全基因组分布。因此,现在可以探索衰老生物体中细胞、组织和器官功能下降可能与表观基因组改变有因果关系的假设。在本文中,我们回顾了干细胞表观遗传调控领域的最新进展,以及这可能有助于衰老。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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