Autophagy: A lysosomal degradation pathway with a central role in health and disease

被引:626
作者
Eskelinen, Eeva-Liisa [1 ]
Saftig, Paul [2 ]
机构
[1] Univ Helsinki, Dept Biol & Environm Sci, Div Biochem, FIN-00014 Helsinki, Finland
[2] Univ Kiel, Inst Biochem, D-24098 Kiel, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2009年 / 1793卷 / 04期
关键词
Autophagy; Lysosome; Phagocytosis; Cancer; Cell death; Neurodegeneration; Aging; ENDOPLASMIC-RETICULUM STRESS; KINASE SIGNALING PATHWAY; ISOLATED RAT HEPATOCYTES; PROGRAMMED CELL-DEATH; MAMMALIAN-CELLS; SACCHAROMYCES-CEREVISIAE; ALZHEIMERS-DISEASE; TUMOR-SUPPRESSOR; NERVOUS-SYSTEM; PROTEIN-KINASE;
D O I
10.1016/j.bbamcr.2008.07.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Autophagy delivers cytoplasmic material and organelles to lysosomes for degradation. The formation of autophagosomes is controlled by a specific set of autophagy genes called atg genes. The magnitude of autophagosome formation is tightly regulated by intracellular and extracellular amino acid concentrations and ATP levels via signaling pathways that include the nutrient sensing kinase TOR. Autophagy functions as a stress response that is upregulated by starvation, oxidative stress, or other harmful conditions. Remarkably, autophagy has been shown to possess important housekeeping and quality control functions that contribute to health and longevity. Autophagy plays a role in innate and adaptive immunity, programmed cell death, as well as prevention of cancer, neurodegeneration and aging. In addition, impaired autophagic degradation contributes to the pathogenesis of several human diseases including lysosomal storage disorders and muscle diseases. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:664 / 673
页数:10
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