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自噬基因与衰老

Autophagy genes and ageing.

作者信息

Vellai T

机构信息

Department of Genetics, Eötvös Loránd University, Budapest H-1117, Hungary.

出版信息

Cell Death Differ. 2009 Jan;16(1):94-102. doi: 10.1038/cdd.2008.126. Epub 2008 Sep 12.

Abstract

Ageing in divergent animal phyla is influenced by several evolutionarily conserved signalling pathways, mitochondrial activity and various environmental factors such as nutrient availability and temperature. Although ageing is a multifactorial process with many mechanisms contributing to the decline, the intracellular accumulation of damaged proteins and mitochondria is a feature common to all aged cells. Autophagy (cellular self-eating) - a lysosome-mediated catabolic process of eukaryotic cells to digest their own constituents - is a major route for the bulk degradation of aberrant cytosolic macromolecules and organelles. Indeed, genetic studies show that autophagy-related genes are required for lifespan extension in various long-lived mutant nematodes and promote survival in worms and flies exposed to prolonged starvation. These data implicate autophagy in ageing control. Furthermore, results in Drosophila demonstrate that promoting basal expression of the autophagy gene Atg8 in the nervous system extends lifespan by 50%, thereby providing evidence that the autophagy pathway regulates the rate at which the tissues age. In this review, the molecular mechanisms by which autophagy genes interact with longevity pathways in diverse organisms ranging from yeast to mammals are discussed.

摘要

不同动物门的衰老受到多种进化上保守的信号通路、线粒体活性以及各种环境因素(如营养可用性和温度)的影响。尽管衰老过程是多因素的,有许多机制导致衰老,但受损蛋白质和线粒体在细胞内的积累是所有衰老细胞共有的特征。自噬(细胞自我吞噬)——真核细胞中一种由溶酶体介导的分解代谢过程,用于消化自身成分——是异常胞质大分子和细胞器大量降解的主要途径。事实上,遗传学研究表明,自噬相关基因是各种长寿突变线虫延长寿命所必需的,并且能促进长期饥饿的蠕虫和果蝇的存活。这些数据表明自噬参与衰老控制。此外,果蝇实验结果表明,促进神经系统中自噬基因Atg8的基础表达可使寿命延长50%,从而证明自噬途径调节组织衰老的速率。在这篇综述中,将讨论自噬基因在从酵母到哺乳动物等不同生物体中与长寿途径相互作用的分子机制。

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