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自噬作为一种细胞降解的调控途径。

Autophagy as a regulated pathway of cellular degradation.

作者信息

Klionsky D J, Emr S D

机构信息

Department of Biology, University of Michigan, 830 North University, Ann Arbor, MI 48109-1048, USA.

出版信息

Science. 2000 Dec 1;290(5497):1717-21. doi: 10.1126/science.290.5497.1717.

DOI:10.1126/science.290.5497.1717
PMID:11099404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2732363/
Abstract

Macroautophagy is a dynamic process involving the rearrangement of subcellular membranes to sequester cytoplasm and organelles for delivery to the lysosome or vacuole where the sequestered cargo is degraded and recycled. This process takes place in all eukaryotic cells. It is highly regulated through the action of various kinases, phosphatases, and guanosine triphosphatases (GTPases). The core protein machinery that is necessary to drive formation and consumption of intermediates in the macroautophagy pathway includes a ubiquitin-like protein conjugation system and a protein complex that directs membrane docking and fusion at the lysosome or vacuole. Macroautophagy plays an important role in developmental processes, human disease, and cellular response to nutrient deprivation.

摘要

巨自噬是一个动态过程,涉及亚细胞膜的重排,以隔离细胞质和细胞器,然后将其输送到溶酶体或液泡,在那里被隔离的物质被降解并循环利用。这个过程发生在所有真核细胞中。它通过各种激酶、磷酸酶和鸟苷三磷酸酶(GTP酶)的作用受到高度调控。驱动巨自噬途径中中间体形成和消耗所必需的核心蛋白质机制包括一个泛素样蛋白质缀合系统和一个指导膜在溶酶体或液泡处对接和融合的蛋白质复合物。巨自噬在发育过程、人类疾病以及细胞对营养剥夺的反应中起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/233e/2732363/fa973d5740d8/nihms15030f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/233e/2732363/45d2671080eb/nihms15030f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/233e/2732363/fa973d5740d8/nihms15030f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/233e/2732363/45d2671080eb/nihms15030f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/233e/2732363/fa973d5740d8/nihms15030f2.jpg

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本文引用的文献

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Autophagy and related mechanisms of lysosome-mediated protein degradation.自噬及溶酶体介导的蛋白质降解相关机制
Trends Cell Biol. 1994 Apr;4(4):139-43. doi: 10.1016/0962-8924(94)90069-8.
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LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing.LC3是酵母Apg8p的哺乳动物同源物,加工后定位于自噬体膜上。
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The reversible modification regulates the membrane-binding state of Apg8/Aut7 essential for autophagy and the cytoplasm to vacuole targeting pathway.
自噬受体NCOA4与E3连接酶HERC2的铁硫簇依赖性相互作用的机制洞察
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Mitochondria as Regulators of Nonapoptotic Cell Death in Cancer.线粒体作为癌症中非凋亡性细胞死亡的调节因子。
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Artemisinin synergizes with CCCP in autophagic cell death induction via ER stress in uveal melanoma.青蒿素与羰基氰氯苯腙(CCCP)协同作用,通过内质网应激诱导葡萄膜黑色素瘤细胞发生自噬性细胞死亡。
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The role of oxidative stress in spinal cord ischemia reperfusion injury: mechanisms and therapeutic implications.氧化应激在脊髓缺血再灌注损伤中的作用:机制及治疗意义
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Exploring the Molecular Mechanisms of Autophagy-related Genes in Hepatic Ischemia/Reperfusion Injury Using Bioinformatics.利用生物信息学探索自噬相关基因在肝脏缺血/再灌注损伤中的分子机制
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这种可逆修饰调节自噬和细胞质到液泡靶向途径所必需的Apg8/Aut7的膜结合状态。
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A Ypt/Rab effector complex containing the Sec1 homolog Vps33p is required for homotypic vacuole fusion.同型液泡融合需要一种包含Sec1同源物Vps33p的Ypt/Rab效应复合物。
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