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Anti-apoptotic BCL-2 family members in development

Almost 30 years ago it was first appreciated that anti-apoptotic B-cell lymphoma-2 (BCL-2) prevents the induction of apoptosis not only in malignant cells, but also in normal cellular lineages. This critical observation has rapidly evolved from merely identifying new BCL-2 family members to understa...

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Autores principales: Opferman, Joseph T, Kothari, Anisha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729530/
https://www.ncbi.nlm.nih.gov/pubmed/29099482
http://dx.doi.org/10.1038/cdd.2017.170
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author Opferman, Joseph T
Kothari, Anisha
author_facet Opferman, Joseph T
Kothari, Anisha
author_sort Opferman, Joseph T
collection PubMed
description Almost 30 years ago it was first appreciated that anti-apoptotic B-cell lymphoma-2 (BCL-2) prevents the induction of apoptosis not only in malignant cells, but also in normal cellular lineages. This critical observation has rapidly evolved from merely identifying new BCL-2 family members to understanding how their biochemical interactions trigger the cell death process, and, more recently, to pharmacological inhibition of anti-apoptotic BCL-2 function in disease. Indeed, the proper regulation of apoptosis is important in many aspects of life including development, homeostasis, and disease biology. To better understand these processes, scientists have used many tools to assess the contribution of individual anti-apoptotic BCL-2 family members. This review will focus on the prominent roles for BCL-2 and other pro-survival family members in promoting the development of mammals during early embryogenesis, neurogenesis, and hematopoiesis.
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spelling pubmed-57295302018-01-01 Anti-apoptotic BCL-2 family members in development Opferman, Joseph T Kothari, Anisha Cell Death Differ Review Almost 30 years ago it was first appreciated that anti-apoptotic B-cell lymphoma-2 (BCL-2) prevents the induction of apoptosis not only in malignant cells, but also in normal cellular lineages. This critical observation has rapidly evolved from merely identifying new BCL-2 family members to understanding how their biochemical interactions trigger the cell death process, and, more recently, to pharmacological inhibition of anti-apoptotic BCL-2 function in disease. Indeed, the proper regulation of apoptosis is important in many aspects of life including development, homeostasis, and disease biology. To better understand these processes, scientists have used many tools to assess the contribution of individual anti-apoptotic BCL-2 family members. This review will focus on the prominent roles for BCL-2 and other pro-survival family members in promoting the development of mammals during early embryogenesis, neurogenesis, and hematopoiesis. Nature Publishing Group 2018-01 2017-11-03 /pmc/articles/PMC5729530/ /pubmed/29099482 http://dx.doi.org/10.1038/cdd.2017.170 Text en Copyright © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Review
Opferman, Joseph T
Kothari, Anisha
Anti-apoptotic BCL-2 family members in development
title Anti-apoptotic BCL-2 family members in development
title_full Anti-apoptotic BCL-2 family members in development
title_fullStr Anti-apoptotic BCL-2 family members in development
title_full_unstemmed Anti-apoptotic BCL-2 family members in development
title_short Anti-apoptotic BCL-2 family members in development
title_sort anti-apoptotic bcl-2 family members in development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729530/
https://www.ncbi.nlm.nih.gov/pubmed/29099482
http://dx.doi.org/10.1038/cdd.2017.170
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