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Autophagy genes and ageing.

机译:自噬基因和衰老。

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摘要

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.
机译:不同动物门的衰老受到几种进化上保守的信号传导途径,线粒体活性以及各种环境因素(例如营养物的利用和温度)的影响。尽管衰老是一个多因素过程,其中许多机制导致衰老,但受损蛋白和线粒体的细胞内积累是所有衰老细胞共有的特征。自噬(细胞自食)-溶酶体介导的真核细胞分解代谢过程,以消化其自身的成分-是大量降解异常胞质大分子和细胞器的主要途径。确实,遗传研究表明,自噬相关基因是延长各种长寿命突变线虫寿命的必需条件,并能促进长期饥饿的蠕虫和果蝇的存活。这些数据意味着老化过程中的自噬。此外,果蝇的研究结果表明,在神经系统中促进自噬基因Atg8的基础表达可延长寿命50%,从而提供证据表明自噬途径可调节组织衰老的速率。在这篇综述中,讨论了自噬基因与从酵母到哺乳动物的各种生物中的长寿途径相互作用的分子机制。

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