Prosurvival AMBRA1 turns into a proapoptotic BH3-like protein during mitochondrial apoptosis

被引:37
作者
Strappazzon, Flavie [1 ]
Di Rita, Anthea [1 ,2 ]
Cianfanelli, Valentina [3 ]
D'Orazio, Melania [2 ]
Nazio, Francesca [1 ,2 ]
Fimia, Gian Maria [4 ,5 ]
Cecconi, Francesco [1 ,2 ,3 ]
机构
[1] IRCCS Fdn Santa Lucia, Rome, Italy
[2] Univ Roma Tor Vergata, Dept Biol, I-00173 Rome, Italy
[3] Danish Canc Soc Res Ctr, Unit Cell Stress & Survival, Copenhagen, Denmark
[4] Univ Salento, Dept Biol & Environm Sci & Technol DiSTeBA, Lecce, Italy
[5] Natl Inst Infect Dis L Spallanzani IRCCS, Rome, Italy
基金
新加坡国家研究基金会;
关键词
AMBRA1; apoptosis; autophagy; BCL2; BH3; domain; MEDIATED CLEAVAGE; CELL-DEATH; AUTOPHAGY; BCL-2; ATG5; CROSSTALK; PARKIN;
D O I
10.1080/15548627.2016.1164359
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
Autophagy and apoptosis are 2 stress-response mechanisms that are closely interconnected. However, the molecular interplays between these 2 pathways remain to be clarified. Here we report that the crucial proautophagic factor AMBRA1 can act as a positive mediator of mitochondrial apoptosis. Indeed, we show that, in a proapoptotic positive feedback loop, the C-terminal part of AMBRA1, generated by CASP/CASPASE cleavage upon apoptosis induction, inhibits the antiapoptotic factor BCL2 by a direct binding through its BH3-like domain. The mitochondrial AMBRA1-BCL2 complex is thus at the crossroad between autophagy and cell death and may represent a novel target in development of therapeutic approaches in clinical diseases.
引用
收藏
页码:963 / 975
页数:13
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