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Necroptosis in development and diseases
Necroptosis, a form of regulated necrotic cell death mediated by RIPK1 (receptor-interacting protein kinase 1) kinase activity, RIPK3, and MLKL (mixed-lineage kinase domain-like pseudokinase), can be activated under apoptosis-deficient conditions. Modulating the activation of RIPK1 by ubiquitination...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900707/ https://www.ncbi.nlm.nih.gov/pubmed/29593066 http://dx.doi.org/10.1101/gad.312561.118 |
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author | Shan, Bing Pan, Heling Najafov, Ayaz Yuan, Junying |
author_facet | Shan, Bing Pan, Heling Najafov, Ayaz Yuan, Junying |
author_sort | Shan, Bing |
collection | PubMed |
description | Necroptosis, a form of regulated necrotic cell death mediated by RIPK1 (receptor-interacting protein kinase 1) kinase activity, RIPK3, and MLKL (mixed-lineage kinase domain-like pseudokinase), can be activated under apoptosis-deficient conditions. Modulating the activation of RIPK1 by ubiquitination and phosphorylation is critical to control both necroptosis and apoptosis. Mutant mice with kinase-dead RIPK1 or RIPK3 and MLKL deficiency show no detrimental phenotype in regard to development and adult homeostasis. However, necroptosis and apoptosis can be activated in response to various mutations that result in the abortion of the defective embryos and human inflammatory and neurodegenerative pathologies. RIPK1 inhibition represents a key therapeutic strategy for treatment of diseases where blocking both necroptosis and apoptosis can be beneficial. |
format | Online Article Text |
id | pubmed-5900707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59007072018-09-01 Necroptosis in development and diseases Shan, Bing Pan, Heling Najafov, Ayaz Yuan, Junying Genes Dev Review Necroptosis, a form of regulated necrotic cell death mediated by RIPK1 (receptor-interacting protein kinase 1) kinase activity, RIPK3, and MLKL (mixed-lineage kinase domain-like pseudokinase), can be activated under apoptosis-deficient conditions. Modulating the activation of RIPK1 by ubiquitination and phosphorylation is critical to control both necroptosis and apoptosis. Mutant mice with kinase-dead RIPK1 or RIPK3 and MLKL deficiency show no detrimental phenotype in regard to development and adult homeostasis. However, necroptosis and apoptosis can be activated in response to various mutations that result in the abortion of the defective embryos and human inflammatory and neurodegenerative pathologies. RIPK1 inhibition represents a key therapeutic strategy for treatment of diseases where blocking both necroptosis and apoptosis can be beneficial. Cold Spring Harbor Laboratory Press 2018-03-01 /pmc/articles/PMC5900707/ /pubmed/29593066 http://dx.doi.org/10.1101/gad.312561.118 Text en © 2018 Shan et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Review Shan, Bing Pan, Heling Najafov, Ayaz Yuan, Junying Necroptosis in development and diseases |
title | Necroptosis in development and diseases |
title_full | Necroptosis in development and diseases |
title_fullStr | Necroptosis in development and diseases |
title_full_unstemmed | Necroptosis in development and diseases |
title_short | Necroptosis in development and diseases |
title_sort | necroptosis in development and diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900707/ https://www.ncbi.nlm.nih.gov/pubmed/29593066 http://dx.doi.org/10.1101/gad.312561.118 |
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