Pore formation in regulated cell death

被引:141
作者
Flores-Romero, Hector [1 ,2 ]
Ros, Uris [1 ,2 ]
Garcia-Saez, Ana J. [1 ,2 ]
机构
[1] Univ Cologne, Inst Genet, Cologne, Germany
[2] Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, Cologne, Germany
基金
欧洲研究理事会;
关键词
apoptosis; cell death; membrane pores; necroptosis; pyroptosis; BAX-DERIVED PEPTIDE; DOMAIN-LIKE PROTEIN; GASDERMIN-D PORE; FORMING PROTEINS; PROAPOPTOTIC BAX; LIPID-BILAYERS; MEMBRANE PORES; CYTOCHROME-C; ANTIMICROBIAL PEPTIDE; MEDIATES NECROPTOSIS;
D O I
10.15252/embj.2020105753
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
The discovery of alternative signaling pathways that regulate cell death has revealed multiple strategies for promoting cell death with diverse consequences at the tissue and organism level. Despite the divergence in the molecular components involved, membrane permeabilization is a common theme in the execution of regulated cell death. In apoptosis, the permeabilization of the outer mitochondrial membrane by BAX and BAK releases apoptotic factors that initiate the caspase cascade and is considered the point of no return in cell death commitment. Pyroptosis and necroptosis also require the perforation of the plasma membrane at the execution step, which involves Gasdermins in pyroptosis, and MLKL in the case of necroptosis. Although BAX/BAK, Gasdermins and MLKL share certain molecular features like oligomerization, they form pores in different cellular membranes via distinct mechanisms. Here, we compare and contrast how BAX/BAK, Gasdermins, and MLKL alter membrane permeability from a structural and biophysical perspective and discuss the general principles of membrane permeabilization in the execution of regulated cell death.
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页数:18
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