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Necroptosis: Fifty shades of RIPKs

Apoptosis and necroptosis are 2 major, yet distinct, forms of regulated cell death. Whereas apoptosis requires caspase protease function, necroptosis requires activation of the receptor interacting protein kinases 1 (RIPK1) and RIPK3. Following activation, RIPK3 phosphorylates mixed-lineage kinase d...

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Detalles Bibliográficos
Autores principales: Ichim, Gabriel, Tait, Stephen WG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905023/
https://www.ncbi.nlm.nih.gov/pubmed/27308415
http://dx.doi.org/10.4161/23723548.2014.965638
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author Ichim, Gabriel
Tait, Stephen WG
author_facet Ichim, Gabriel
Tait, Stephen WG
author_sort Ichim, Gabriel
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description Apoptosis and necroptosis are 2 major, yet distinct, forms of regulated cell death. Whereas apoptosis requires caspase protease function, necroptosis requires activation of the receptor interacting protein kinases 1 (RIPK1) and RIPK3. Following activation, RIPK3 phosphorylates mixed-lineage kinase domain-like (MLKL), leading to cell death. Apoptosis and necroptosis are deeply intertwined such that a given death stimulus can often engage either form of cell death. Recent studies published in Cell Death and Differentiation by the Han, Oberst, and Vaux laboratories provide exciting new insights into necroptosis and how it interconnects with apoptosis. As we will discuss, their findings address key questions including: How does a cell choose between apoptosis or necroptosis? How can RIPK3 also induce apoptosis? What is the nature of the RIPK1–3 signaling cascade leading to necroptosis? Finally, data from the Oberst and Han groups strongly argue that RIPK1 is not only involved in executing necroptosis, but also protects against this process in some settings.
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spelling pubmed-49050232016-06-15 Necroptosis: Fifty shades of RIPKs Ichim, Gabriel Tait, Stephen WG Mol Cell Oncol Commentary Apoptosis and necroptosis are 2 major, yet distinct, forms of regulated cell death. Whereas apoptosis requires caspase protease function, necroptosis requires activation of the receptor interacting protein kinases 1 (RIPK1) and RIPK3. Following activation, RIPK3 phosphorylates mixed-lineage kinase domain-like (MLKL), leading to cell death. Apoptosis and necroptosis are deeply intertwined such that a given death stimulus can often engage either form of cell death. Recent studies published in Cell Death and Differentiation by the Han, Oberst, and Vaux laboratories provide exciting new insights into necroptosis and how it interconnects with apoptosis. As we will discuss, their findings address key questions including: How does a cell choose between apoptosis or necroptosis? How can RIPK3 also induce apoptosis? What is the nature of the RIPK1–3 signaling cascade leading to necroptosis? Finally, data from the Oberst and Han groups strongly argue that RIPK1 is not only involved in executing necroptosis, but also protects against this process in some settings. Taylor & Francis 2014-11-07 /pmc/articles/PMC4905023/ /pubmed/27308415 http://dx.doi.org/10.4161/23723548.2014.965638 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Commentary
Ichim, Gabriel
Tait, Stephen WG
Necroptosis: Fifty shades of RIPKs
title Necroptosis: Fifty shades of RIPKs
title_full Necroptosis: Fifty shades of RIPKs
title_fullStr Necroptosis: Fifty shades of RIPKs
title_full_unstemmed Necroptosis: Fifty shades of RIPKs
title_short Necroptosis: Fifty shades of RIPKs
title_sort necroptosis: fifty shades of ripks
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905023/
https://www.ncbi.nlm.nih.gov/pubmed/27308415
http://dx.doi.org/10.4161/23723548.2014.965638
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