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自噬在细胞内病原体营养获取中的作用。

The role of autophagy in intracellular pathogen nutrient acquisition.

作者信息

Steele Shaun, Brunton Jason, Kawula Thomas

机构信息

Department of Microbiology and Immunology, School of Medicine, University of North Carolina Chapel Hill, NC, USA.

出版信息

Front Cell Infect Microbiol. 2015 Jun 9;5:51. doi: 10.3389/fcimb.2015.00051. eCollection 2015.

Abstract

Following entry into host cells intracellular pathogens must simultaneously evade innate host defense mechanisms and acquire energy and anabolic substrates from the nutrient-limited intracellular environment. Most of the potential intracellular nutrient sources are stored within complex macromolecules that are not immediately accessible by intracellular pathogens. To obtain nutrients for proliferation, intracellular pathogens must compete with the host cell for newly-imported simple nutrients or degrade host nutrient storage structures into their constituent components (fatty acids, carbohydrates, and amino acids). It is becoming increasingly evident that intracellular pathogens have evolved a wide variety of strategies to accomplish this task. One recurrent microbial strategy is to exploit host degradative processes that break down host macromolecules into simple nutrients that the microbe can use. Herein we focus on how a subset of bacterial, viral, and eukaryotic pathogens leverage the host process of autophagy to acquire nutrients that support their growth within infected cells.

摘要

进入宿主细胞后,细胞内病原体必须同时逃避宿主的固有防御机制,并从营养有限的细胞内环境中获取能量和合成代谢底物。大多数潜在的细胞内营养源都储存在复杂的大分子中,细胞内病原体无法立即获取这些营养源。为了获取用于增殖的营养物质,细胞内病原体必须与宿主细胞竞争新导入的简单营养物质,或者将宿主营养储存结构降解为其组成成分(脂肪酸、碳水化合物和氨基酸)。越来越明显的是,细胞内病原体已经进化出多种策略来完成这项任务。一种常见的微生物策略是利用宿主的降解过程,将宿主大分子分解为微生物可以利用的简单营养物质。在此,我们重点关注细菌、病毒和真核病原体的一个子集如何利用宿主的自噬过程来获取支持其在受感染细胞内生长的营养物质。

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本文引用的文献

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Cell Host Microbe. 2015 Apr 8;17(4):515-25. doi: 10.1016/j.chom.2015.02.008. Epub 2015 Mar 12.
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Annu Rev Biophys. 2015;44:101-22. doi: 10.1146/annurev-biophys-060414-034248. Epub 2015 Feb 26.
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Metabolic control of autophagy.自噬的代谢调控
Cell. 2014 Dec 4;159(6):1263-76. doi: 10.1016/j.cell.2014.11.006.

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