Autophagy and human disease

被引:300
作者
Huang, Ju
Klionsky, Daniel J. [1 ]
机构
[1] Univ Michigan, Life Sci Ctr, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Life Sci Ctr, Dept Biol Chem, Ann Arbor, MI 48109 USA
关键词
lysosome; protein targeting; vacuole; yeast;
D O I
10.4161/cc.6.15.4511
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As a conserved cellular degradative pathway in eukaryotes, autophagy relieves cells from various types of stress. There are different forms of autophagy, and the ongoing studies of the molecular mechanisms and cellular functions of these processes are unraveling their significant roles in human health. Currently, the best-studied of these pathways is macroautophagy, which is linked to a range of human disease. For example, as part of the host immune defense mechanism, macroautophagy is activated to eliminate invasive pathogenic bacteria; however, in some cases bacteria subvert this process for their own replication. Autophagy also contributes to endogenous major histocompatibility complex class II antigen presentation, reflecting its role in adaptive immunity. In certain neurodegenerative diseases, which are associated with aggregation-prone proteins, macroautophagy plays a protective role in preventing or reducing cytotoxicity by clearance of the toxic proteins; however, the autophagy-dependent processing of some components correlates with the pathogenesis of certain myopathies. Finally, autophagy acts as a mechanism for tumor suppression, although some cancer cells use it as a cytoprotective mechanism. Thus, a fundamental paradox of autophagy is that it can act to promote both cell survival and cell death, depending on the specific conditions.
引用
收藏
页码:1837 / 1849
页数:13
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