Cargando…
Evolution and function of the epithelial cell-specific ER stress sensor IRE1β
Barrier epithelial cells lining the mucosal surfaces of the gastrointestinal and respiratory tracts interface directly with the environment. As such, these tissues are continuously challenged to maintain a healthy equilibrium between immunity and tolerance against environmental toxins, food componen...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528705/ https://www.ncbi.nlm.nih.gov/pubmed/34075183 http://dx.doi.org/10.1038/s41385-021-00412-8 |
_version_ | 1784586305329430528 |
---|---|
author | Cloots, Eva Simpson, Mariska S. De Nolf, Clint Lencer, Wayne I. Janssens, Sophie Grey, Michael J. |
author_facet | Cloots, Eva Simpson, Mariska S. De Nolf, Clint Lencer, Wayne I. Janssens, Sophie Grey, Michael J. |
author_sort | Cloots, Eva |
collection | PubMed |
description | Barrier epithelial cells lining the mucosal surfaces of the gastrointestinal and respiratory tracts interface directly with the environment. As such, these tissues are continuously challenged to maintain a healthy equilibrium between immunity and tolerance against environmental toxins, food components, and microbes. An extracellular mucus barrier, produced and secreted by the underlying epithelium plays a central role in this host defense response. Several dedicated molecules with a unique tissue-specific expression in mucosal epithelia govern mucosal homeostasis. Here, we review the biology of Inositol-requiring enzyme 1β (IRE1β), an ER-resident endonuclease and paralogue of the most evolutionarily conserved ER stress sensor IRE1α. IRE1β arose through gene duplication in early vertebrates and adopted functions unique from IRE1α which appear to underlie the basic development and physiology of mucosal tissues. |
format | Online Article Text |
id | pubmed-8528705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-85287052021-11-01 Evolution and function of the epithelial cell-specific ER stress sensor IRE1β Cloots, Eva Simpson, Mariska S. De Nolf, Clint Lencer, Wayne I. Janssens, Sophie Grey, Michael J. Mucosal Immunol Review Article Barrier epithelial cells lining the mucosal surfaces of the gastrointestinal and respiratory tracts interface directly with the environment. As such, these tissues are continuously challenged to maintain a healthy equilibrium between immunity and tolerance against environmental toxins, food components, and microbes. An extracellular mucus barrier, produced and secreted by the underlying epithelium plays a central role in this host defense response. Several dedicated molecules with a unique tissue-specific expression in mucosal epithelia govern mucosal homeostasis. Here, we review the biology of Inositol-requiring enzyme 1β (IRE1β), an ER-resident endonuclease and paralogue of the most evolutionarily conserved ER stress sensor IRE1α. IRE1β arose through gene duplication in early vertebrates and adopted functions unique from IRE1α which appear to underlie the basic development and physiology of mucosal tissues. Nature Publishing Group US 2021-06-01 2021 /pmc/articles/PMC8528705/ /pubmed/34075183 http://dx.doi.org/10.1038/s41385-021-00412-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Cloots, Eva Simpson, Mariska S. De Nolf, Clint Lencer, Wayne I. Janssens, Sophie Grey, Michael J. Evolution and function of the epithelial cell-specific ER stress sensor IRE1β |
title | Evolution and function of the epithelial cell-specific ER stress sensor IRE1β |
title_full | Evolution and function of the epithelial cell-specific ER stress sensor IRE1β |
title_fullStr | Evolution and function of the epithelial cell-specific ER stress sensor IRE1β |
title_full_unstemmed | Evolution and function of the epithelial cell-specific ER stress sensor IRE1β |
title_short | Evolution and function of the epithelial cell-specific ER stress sensor IRE1β |
title_sort | evolution and function of the epithelial cell-specific er stress sensor ire1β |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528705/ https://www.ncbi.nlm.nih.gov/pubmed/34075183 http://dx.doi.org/10.1038/s41385-021-00412-8 |
work_keys_str_mv | AT clootseva evolutionandfunctionoftheepithelialcellspecificerstresssensorire1b AT simpsonmariskas evolutionandfunctionoftheepithelialcellspecificerstresssensorire1b AT denolfclint evolutionandfunctionoftheepithelialcellspecificerstresssensorire1b AT lencerwaynei evolutionandfunctionoftheepithelialcellspecificerstresssensorire1b AT janssenssophie evolutionandfunctionoftheepithelialcellspecificerstresssensorire1b AT greymichaelj evolutionandfunctionoftheepithelialcellspecificerstresssensorire1b |