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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...

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Detalles Bibliográficos
Autores principales: Denecker, Geertrui, Ovaere, Petra, Vandenabeele, Peter, Declercq, Wim
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2008
Materias:
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.
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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
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