自噬
神经退行性变
细胞生物学
ATG16L1
生物
细胞器
副现象
疾病
神经科学
医学
生物化学
细胞凋亡
病理
认识论
哲学
作者
Brinda Ravikumar,Sovan Sarkar,J. Eric Davies,Marie Futter,Moisés Garcı́a-Arencibia,Zeyn W. Green-Thompson,María Jiménez-Sánchez,Viktor I. Korolchuk,Maike Lichtenberg,Shouqing Luo,Dunecan Massey,Fiona M. Menzies,Kévin Moreau,Usha Narayanan,Maurizio Renna,Farah H. Siddiqi,Benjamin R. Underwood,Ashley R. Winslow,David C. Rubinsztein
出处
期刊:Physiological Reviews
[American Physiological Society]
日期:2010-10-01
卷期号:90 (4): 1383-1435
被引量:1659
标识
DOI:10.1152/physrev.00030.2009
摘要
(Macro)autophagy is a bulk degradation process that mediates the clearance of long-lived proteins and organelles. Autophagy is initiated by double-membraned structures, which engulf portions of cytoplasm. The resulting autophagosomes ultimately fuse with lysosomes, where their contents are degraded. Although the term autophagy was first used in 1963, the field has witnessed dramatic growth in the last 5 years, partly as a consequence of the discovery of key components of its cellular machinery. In this review we focus on mammalian autophagy, and we give an overview of the understanding of its machinery and the signaling cascades that regulate it. As recent studies have also shown that autophagy is critical in a range of normal human physiological processes, and defective autophagy is associated with diverse diseases, including neurodegeneration, lysosomal storage diseases, cancers, and Crohn's disease, we discuss the roles of autophagy in health and disease, while trying to critically evaluate if the coincidence between autophagy and these conditions is causal or an epiphenomenon. Finally, we consider the possibility of autophagy upregulation as a therapeutic approach for various conditions.
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