Cargando…

Death-effector Filaments: Novel Cytoplasmic Structures that Recruit Caspases and Trigger Apoptosis

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 Pro...

Descripción completa

Detalles Bibliográficos
Autores principales: Siegel, Richard M., Martin, David A., Zheng, Lixin, Ng, Samuel Y., Bertin, John, Cohen, Jeffrey, Lenardo, Michael J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137190/
https://www.ncbi.nlm.nih.gov/pubmed/9606215
_version_ 1782143273837527040
author Siegel, Richard M.
Martin, David A.
Zheng, Lixin
Ng, Samuel Y.
Bertin, John
Cohen, Jeffrey
Lenardo, Michael J.
author_facet Siegel, Richard M.
Martin, David A.
Zheng, Lixin
Ng, Samuel Y.
Bertin, John
Cohen, Jeffrey
Lenardo, Michael J.
author_sort Siegel, Richard M.
collection PubMed
description 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.
format Text
id pubmed-2137190
institution National Center for Biotechnology Information
language English
publishDate 1998
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21371902008-05-01 Death-effector Filaments: Novel Cytoplasmic Structures that Recruit Caspases and Trigger Apoptosis Siegel, Richard M. Martin, David A. Zheng, Lixin Ng, Samuel Y. Bertin, John Cohen, Jeffrey Lenardo, Michael J. J Cell Biol Articles 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. The Rockefeller University Press 1998-06-01 /pmc/articles/PMC2137190/ /pubmed/9606215 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Siegel, Richard M.
Martin, David A.
Zheng, Lixin
Ng, Samuel Y.
Bertin, John
Cohen, Jeffrey
Lenardo, Michael J.
Death-effector Filaments: Novel Cytoplasmic Structures that Recruit Caspases and Trigger Apoptosis
title Death-effector Filaments: Novel Cytoplasmic Structures that Recruit Caspases and Trigger Apoptosis
title_full Death-effector Filaments: Novel Cytoplasmic Structures that Recruit Caspases and Trigger Apoptosis
title_fullStr Death-effector Filaments: Novel Cytoplasmic Structures that Recruit Caspases and Trigger Apoptosis
title_full_unstemmed Death-effector Filaments: Novel Cytoplasmic Structures that Recruit Caspases and Trigger Apoptosis
title_short Death-effector Filaments: Novel Cytoplasmic Structures that Recruit Caspases and Trigger Apoptosis
title_sort death-effector filaments: novel cytoplasmic structures that recruit caspases and trigger apoptosis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137190/
https://www.ncbi.nlm.nih.gov/pubmed/9606215
work_keys_str_mv AT siegelrichardm deatheffectorfilamentsnovelcytoplasmicstructuresthatrecruitcaspasesandtriggerapoptosis
AT martindavida deatheffectorfilamentsnovelcytoplasmicstructuresthatrecruitcaspasesandtriggerapoptosis
AT zhenglixin deatheffectorfilamentsnovelcytoplasmicstructuresthatrecruitcaspasesandtriggerapoptosis
AT ngsamuely deatheffectorfilamentsnovelcytoplasmicstructuresthatrecruitcaspasesandtriggerapoptosis
AT bertinjohn deatheffectorfilamentsnovelcytoplasmicstructuresthatrecruitcaspasesandtriggerapoptosis
AT cohenjeffrey deatheffectorfilamentsnovelcytoplasmicstructuresthatrecruitcaspasesandtriggerapoptosis
AT lenardomichaelj deatheffectorfilamentsnovelcytoplasmicstructuresthatrecruitcaspasesandtriggerapoptosis