Death-effector filaments: Novel cytoplasmic structures that recruit caspases and trigger apoptosis

被引:210
作者
Siegel, RM
Martin, DA
Zheng, LX
Ng, SY
Bertin, J
Cohen, J
Lenardo, MJ
机构
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Clin Invest Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1083/jcb.141.5.1243
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The death-effector domain (DED) is a critical protein interaction domain that recruits caspases into complexes with members of the TNF-receptor superfamily. Apoptosis can also be induced by expressing certain DED-containing proteins without surface receptor cross-linking. Using Green Fluorescent Protein to examine DED-containing proteins in living cells, we show that these proteins cause apoptosis by forming novel cytoplasmic filaments that recruit and activate pro-caspase zymogens. Formation of these filaments, which we term death-effector filaments, was blocked by coexpression of viral antiapoptotic DED-containing proteins, but not by bcl-2 family proteins. Thus, formation of death-effector filaments allows a regulated intracellular assembly of apoptosis-signaling complexes that can initiate or amplify apoptotic stimuli independently of receptors at the plasma membrane.
引用
收藏
页码:1243 / 1253
页数:11
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