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Caspase-14 reveals its secrets
Caspase-14 is a unique member of the evolutionarily conserved family of cysteinyl aspartate–specific proteinases, which are mainly involved in inflammation and apoptosis. However, recent evidence also implicates these proteases in proliferation and differentiation. Although most caspases are ubiquit...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2234247/ https://www.ncbi.nlm.nih.gov/pubmed/18250198 http://dx.doi.org/10.1083/jcb.200709098 |
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author | Denecker, Geertrui Ovaere, Petra Vandenabeele, Peter Declercq, Wim |
author_facet | Denecker, Geertrui Ovaere, Petra Vandenabeele, Peter Declercq, Wim |
author_sort | Denecker, Geertrui |
collection | PubMed |
description | Caspase-14 is a unique member of the evolutionarily conserved family of cysteinyl aspartate–specific proteinases, which are mainly involved in inflammation and apoptosis. However, recent evidence also implicates these proteases in proliferation and differentiation. Although most caspases are ubiquitously expressed, caspase-14 expression is confined mainly to cornifying epithelia, such as the skin. Moreover, caspase-14 activation correlates with cornification, indicating that it plays a role in terminal keratinocyte differentiation. The determination of in vitro conditions for caspase-14 activity paved the way to identifying its substrates. The recent development of caspase-14–deficient mice underscored its importance in the correct degradation of (pro)filaggrin and in the formation of the epidermal barrier that protects against dehydration and UVB radiation. Here, we review the current knowledge on caspase-14 in skin homeostasis and disease. |
format | Text |
id | pubmed-2234247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22342472008-08-11 Caspase-14 reveals its secrets Denecker, Geertrui Ovaere, Petra Vandenabeele, Peter Declercq, Wim J Cell Biol Reviews Caspase-14 is a unique member of the evolutionarily conserved family of cysteinyl aspartate–specific proteinases, which are mainly involved in inflammation and apoptosis. However, recent evidence also implicates these proteases in proliferation and differentiation. Although most caspases are ubiquitously expressed, caspase-14 expression is confined mainly to cornifying epithelia, such as the skin. Moreover, caspase-14 activation correlates with cornification, indicating that it plays a role in terminal keratinocyte differentiation. The determination of in vitro conditions for caspase-14 activity paved the way to identifying its substrates. The recent development of caspase-14–deficient mice underscored its importance in the correct degradation of (pro)filaggrin and in the formation of the epidermal barrier that protects against dehydration and UVB radiation. Here, we review the current knowledge on caspase-14 in skin homeostasis and disease. The Rockefeller University Press 2008-02-11 /pmc/articles/PMC2234247/ /pubmed/18250198 http://dx.doi.org/10.1083/jcb.200709098 Text en Copyright © 2008, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Reviews Denecker, Geertrui Ovaere, Petra Vandenabeele, Peter Declercq, Wim Caspase-14 reveals its secrets |
title | Caspase-14 reveals its secrets |
title_full | Caspase-14 reveals its secrets |
title_fullStr | Caspase-14 reveals its secrets |
title_full_unstemmed | Caspase-14 reveals its secrets |
title_short | Caspase-14 reveals its secrets |
title_sort | caspase-14 reveals its secrets |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2234247/ https://www.ncbi.nlm.nih.gov/pubmed/18250198 http://dx.doi.org/10.1083/jcb.200709098 |
work_keys_str_mv | AT deneckergeertrui caspase14revealsitssecrets AT ovaerepetra caspase14revealsitssecrets AT vandenabeelepeter caspase14revealsitssecrets AT declercqwim caspase14revealsitssecrets |