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The BH3-only protein Bad is dispensable for TNF-mediated cell death

Tumor necrosis factor (TNF) is a key signaling molecule orchestrating immune and inflammatory responses and possesses the capacity to trigger apoptotic as well as necroptotic cell death. Apoptotic cell death elicited by TNF has been demonstrated to engage pro-apoptotic Bcl-2 family proteins, most pr...

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Detalles Bibliográficos
Autores principales: Ottina, E, Sochalska, M, Sgonc, R, Villunger, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669773/
https://www.ncbi.nlm.nih.gov/pubmed/25611386
http://dx.doi.org/10.1038/cddis.2014.575
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author Ottina, E
Sochalska, M
Sgonc, R
Villunger, A
author_facet Ottina, E
Sochalska, M
Sgonc, R
Villunger, A
author_sort Ottina, E
collection PubMed
description Tumor necrosis factor (TNF) is a key signaling molecule orchestrating immune and inflammatory responses and possesses the capacity to trigger apoptotic as well as necroptotic cell death. Apoptotic cell death elicited by TNF has been demonstrated to engage pro-apoptotic Bcl-2 family proteins, most prominently the BH3-only protein Bid, a key substrate of caspase-8, the key effector protease downstream of TNF receptor I. Most recently, the BH3 domain-containing protein Bad (Bcl-2-antagonist of cell death) has been shown to be rate limiting for TNF-mediated cell death, suggesting possible synergy with Bid, but genetic analyses presented here demonstrate that it is dispensable for this process.
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spelling pubmed-46697732015-12-08 The BH3-only protein Bad is dispensable for TNF-mediated cell death Ottina, E Sochalska, M Sgonc, R Villunger, A Cell Death Dis Original Article Tumor necrosis factor (TNF) is a key signaling molecule orchestrating immune and inflammatory responses and possesses the capacity to trigger apoptotic as well as necroptotic cell death. Apoptotic cell death elicited by TNF has been demonstrated to engage pro-apoptotic Bcl-2 family proteins, most prominently the BH3-only protein Bid, a key substrate of caspase-8, the key effector protease downstream of TNF receptor I. Most recently, the BH3 domain-containing protein Bad (Bcl-2-antagonist of cell death) has been shown to be rate limiting for TNF-mediated cell death, suggesting possible synergy with Bid, but genetic analyses presented here demonstrate that it is dispensable for this process. Nature Publishing Group 2015-01 2015-01-22 /pmc/articles/PMC4669773/ /pubmed/25611386 http://dx.doi.org/10.1038/cddis.2014.575 Text en Copyright © 2015 Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International Licence. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons licence, users will need to obtain permission from the licence holder to reproduce the material. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0
spellingShingle Original Article
Ottina, E
Sochalska, M
Sgonc, R
Villunger, A
The BH3-only protein Bad is dispensable for TNF-mediated cell death
title The BH3-only protein Bad is dispensable for TNF-mediated cell death
title_full The BH3-only protein Bad is dispensable for TNF-mediated cell death
title_fullStr The BH3-only protein Bad is dispensable for TNF-mediated cell death
title_full_unstemmed The BH3-only protein Bad is dispensable for TNF-mediated cell death
title_short The BH3-only protein Bad is dispensable for TNF-mediated cell death
title_sort bh3-only protein bad is dispensable for tnf-mediated cell death
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669773/
https://www.ncbi.nlm.nih.gov/pubmed/25611386
http://dx.doi.org/10.1038/cddis.2014.575
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