Connexins modulate autophagosome biogenesis

被引:134
作者
Bejarano, Eloy [1 ,2 ]
Yuste, Andrea [1 ,2 ]
Patel, Bindi [1 ,2 ]
Stout, Randy F., Jr. [3 ]
Spray, David C. [3 ]
Cuervo, Ana Maria [1 ,2 ]
机构
[1] Albert Einstein Coll Med, Dept Dev & Mol Biol, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Inst Aging Studies, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Dominick P Purpura Dept Neurosci, Bronx, NY 10461 USA
关键词
PHOSPHATIDYLINOSITOL; 3-PHOSPHATE; PLASMA-MEMBRANE; GAP-JUNCTIONS; RAT-LIVER; PATHWAY; PHOSPHORYLATION; CONTRIBUTES; ENDOCYTOSIS; INHIBITION; MATURATION;
D O I
10.1038/ncb2934
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The plasma membrane contributes to the formation of autophagosomes, the double-membrane vesicles that sequester cytosolic cargo and deliver it to lysosomes for degradation during autophagy. In this study, we have identified a regulatory role for connexins (Cx), the main components of plasma membrane gap junctions, in autophagosome formation. We have found that plasma-membrane-localized Cx proteins constitutively downregulate autophagy through a direct interaction with several autophagy-related proteins involved in the initial steps of autophagosome formation, such as Atg 16 and components of the PI(3) K autophagy initiation complex (Vps34, Beclin-1 and Vps15). On nutrient starvation, this inhibitory effect is released by the arrival of Atg 14 to the Cx-Atg complex. This promotes the internalization of Cx-Atg along with Atg9, which is also recruited to the plasma membrane in response to starvation. Maturation of the Cx-containing pre-autophagosomes into autophagosomes leads to degradation of these endogenous inhibitors, allowing for sustained activation of autophagy.
引用
收藏
页码:401 / U55
页数:25
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