衰老过程中自噬的转录调控

IF 2.5 Q2 PHYSIOLOGY
Tatiana M Moreno , Caitlin M Lange , Caroline Kumsta
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引用次数: 1

摘要

巨噬,简称自噬,是一种降解受损细胞成分的细胞再循环过程。自噬对维持细胞稳态很重要,据报道随着年龄的增长而下降。这种与年龄相关的自噬功能降低与年龄相关疾病的发展有关。感知营养状态和细胞应激的信号通路网络通过翻译后、转录和表观遗传机制调节自噬,但导致自噬随年龄下降的分子机制尚不清楚。在这里,我们回顾了自噬与衰老之间的联系,并重点讨论了关键自噬基因的转录失调导致自噬与年龄相关的下降的假设。我们概述了转录因子TFEB(转录因子EB)和FOXOs(叉头盒o家族蛋白)如何促进健康生物体中自噬的适当转录调节,并总结了转录因子功能调节的年龄相关变化的最新进展,这些变化可能导致自噬的转录失调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptional regulation of autophagy in aging

Macroautophagy, hereafter autophagy, is a cellular recycling process that degrades damaged cellular components. Autophagy is important for maintaining cellular homeostasis and has been reported to decline with age. This age-related reduction in autophagy function has been associated with the development of age-related diseases. A network of signaling pathways that sense nutrient status and cellular stress regulate autophagy via post-translational, transcriptional, and epigenetic mechanisms, but the molecular mechanisms that lead to autophagy decline with age remain unclear. Here, we review links between autophagy and aging and focus on the hypothesis that transcriptional dysregulation of key autophagy genes contributes to the age-related decline in autophagy. We outline how transcription factors TFEB (transcription factor EB) and FOXOs ( forkhead box-O family proteins) facilitate appropriate transcriptional regulation of autophagy in healthy organisms, and summarize recent advances characterizing age-related changes in the regulation of transcription-factor function that could contribute to transcriptional dysregulation of autophagy.

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来源期刊
Current Opinion in Physiology
Current Opinion in Physiology Medicine-Physiology (medical)
CiteScore
5.80
自引率
0.00%
发文量
52
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