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Channelling inflammation: gasdermins in physiology and disease
Gasdermins were recently identified as the mediators of pyroptosis — inflammatory cell death triggered by cytosolic sensing of invasive infection and danger signals. Upon activation, gasdermins form cell membrane pores, which release pro-inflammatory cytokines and alarmins and damage the integrity o...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944254/ https://www.ncbi.nlm.nih.gov/pubmed/33692549 http://dx.doi.org/10.1038/s41573-021-00154-z |
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author | Liu, Xing Xia, Shiyu Zhang, Zhibin Wu, Hao Lieberman, Judy |
author_facet | Liu, Xing Xia, Shiyu Zhang, Zhibin Wu, Hao Lieberman, Judy |
author_sort | Liu, Xing |
collection | PubMed |
description | Gasdermins were recently identified as the mediators of pyroptosis — inflammatory cell death triggered by cytosolic sensing of invasive infection and danger signals. Upon activation, gasdermins form cell membrane pores, which release pro-inflammatory cytokines and alarmins and damage the integrity of the cell membrane. Roles for gasdermins in autoimmune and inflammatory diseases, infectious diseases, deafness and cancer are emerging, revealing potential novel therapeutic avenues. Here, we review current knowledge of the family of gasdermins, focusing on their mechanisms of action and roles in normal physiology and disease. Efforts to develop drugs to modulate gasdermin activity to reduce inflammation or activate more potent immune responses are highlighted. |
format | Online Article Text |
id | pubmed-7944254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79442542021-03-10 Channelling inflammation: gasdermins in physiology and disease Liu, Xing Xia, Shiyu Zhang, Zhibin Wu, Hao Lieberman, Judy Nat Rev Drug Discov Review Article Gasdermins were recently identified as the mediators of pyroptosis — inflammatory cell death triggered by cytosolic sensing of invasive infection and danger signals. Upon activation, gasdermins form cell membrane pores, which release pro-inflammatory cytokines and alarmins and damage the integrity of the cell membrane. Roles for gasdermins in autoimmune and inflammatory diseases, infectious diseases, deafness and cancer are emerging, revealing potential novel therapeutic avenues. Here, we review current knowledge of the family of gasdermins, focusing on their mechanisms of action and roles in normal physiology and disease. Efforts to develop drugs to modulate gasdermin activity to reduce inflammation or activate more potent immune responses are highlighted. Nature Publishing Group UK 2021-03-10 2021 /pmc/articles/PMC7944254/ /pubmed/33692549 http://dx.doi.org/10.1038/s41573-021-00154-z Text en © Springer Nature Limited 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Article Liu, Xing Xia, Shiyu Zhang, Zhibin Wu, Hao Lieberman, Judy Channelling inflammation: gasdermins in physiology and disease |
title | Channelling inflammation: gasdermins in physiology and disease |
title_full | Channelling inflammation: gasdermins in physiology and disease |
title_fullStr | Channelling inflammation: gasdermins in physiology and disease |
title_full_unstemmed | Channelling inflammation: gasdermins in physiology and disease |
title_short | Channelling inflammation: gasdermins in physiology and disease |
title_sort | channelling inflammation: gasdermins in physiology and disease |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944254/ https://www.ncbi.nlm.nih.gov/pubmed/33692549 http://dx.doi.org/10.1038/s41573-021-00154-z |
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