Siegel R M, Martin D A, Zheng L, Ng S Y, Bertin J, Cohen J, Lenardo M J
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Cell Biol. 1998 Jun 1;141(5):1243-53. doi: 10.1083/jcb.141.5.1243.
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.
死亡效应结构域(DED)是一种关键的蛋白质相互作用结构域,可将半胱天冬酶募集到与肿瘤坏死因子受体超家族成员形成的复合物中。在不进行表面受体交联的情况下,表达某些含DED的蛋白质也可诱导细胞凋亡。利用绿色荧光蛋白检测活细胞中的含DED蛋白质,我们发现这些蛋白质通过形成新的细胞质细丝来诱导细胞凋亡,这些细丝募集并激活前半胱天冬酶原。我们将这些细丝称为死亡效应细丝,病毒含抗凋亡DED蛋白质的共表达可阻断这些细丝的形成,但bcl-2家族蛋白质则不能。因此,死亡效应细丝的形成允许凋亡信号复合物在细胞内进行有序组装,从而能够独立于质膜上的受体启动或放大凋亡刺激。