Regulation of macroautophagy by mTOR and Beclin 1 complexes

被引:444
作者
Pattingre, Sophie [1 ,2 ]
Espert, Lucile [3 ]
Biard-Piechaczyk, Martine [3 ]
Codogno, Patrice [1 ,2 ]
机构
[1] INSERM, U756, F-92296 Chatenay Malabry, France
[2] Univ Paris 11, Fac Pharm, F-92296 Chatenay Malabry, France
[3] Inst Biol, CNRS, UM2, UM1,CPBS, F-34965 Montpellier, France
关键词
autophagy; Beclin; 1; mTOR; lysosome; signal transduction;
D O I
10.1016/j.biochi.2007.08.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macroautophagy or autophagy is a vacuolar degradative pathway terminating in the lysosomal compartment after forming a cytoplasmic vacuole or autophagosome that engulfs macromolecules and organelles. The original discovery that ATG (AuTophaGy related) genes in yeast are involved in the formation of autophagosomes has greatly increased our knowledge of the molecular basis of autophagy, and its role in cell function that extends far beyond non-selective degradation. The regulation of autophagy by signaling pathways overlaps the control of cell growth, proliferation, cell survival and death. The evolutionarily conserved TOR (Target of Rapamycin) kinase complex 1 plays an important role upstream of the Atg 1 complex in the control of autophagy by growth factors, nutrients, calcium signaling and in response to stress situations, including hypoxia, oxidative stress and low energy. The Beclin 1 (Atg6) complex, which is involved in the initial step of autophagosome formation, is directly targeted by signaling pathways. Taken together, these data suggest that multiple signaling checkpoints are involved in regulating autophagosome formation. (c) 2007 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:313 / 323
页数:11
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