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Matriptase zymogen supports epithelial development, homeostasis and regeneration
BACKGROUND: Matriptase is a membrane serine protease essential for epithelial development, homeostasis, and regeneration, as well as a central orchestrator of pathogenic pericellular signaling in the context of inflammatory and proliferative diseases. Matriptase is an unusual protease in that its zy...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452369/ https://www.ncbi.nlm.nih.gov/pubmed/28571576 http://dx.doi.org/10.1186/s12915-017-0384-4 |
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author | Friis, Stine Tadeo, Daniel Le-Gall, Sylvain M. Jürgensen, Henrik Jessen Sales, Katiuchia Uzzun Camerer, Eric Bugge, Thomas H. |
author_facet | Friis, Stine Tadeo, Daniel Le-Gall, Sylvain M. Jürgensen, Henrik Jessen Sales, Katiuchia Uzzun Camerer, Eric Bugge, Thomas H. |
author_sort | Friis, Stine |
collection | PubMed |
description | BACKGROUND: Matriptase is a membrane serine protease essential for epithelial development, homeostasis, and regeneration, as well as a central orchestrator of pathogenic pericellular signaling in the context of inflammatory and proliferative diseases. Matriptase is an unusual protease in that its zymogen displays measurable enzymatic activity. RESULTS: Here, we used gain and loss of function genetics to investigate the possible biological functions of zymogen matriptase. Unexpectedly, transgenic mice mis-expressing a zymogen-locked version of matriptase in the epidermis displayed pathologies previously reported for transgenic mice mis-expressing wildtype epidermal matriptase. Equally surprising, mice engineered to express only zymogen-locked endogenous matriptase, unlike matriptase null mice, were viable, developed epithelial barrier function, and regenerated the injured epithelium. Compatible with these observations, wildtype and zymogen-locked matriptase were equipotent activators of PAR-2 inflammatory signaling. CONCLUSION: The study demonstrates that the matriptase zymogen is biologically active and is capable of executing developmental and homeostatic functions of the protease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-017-0384-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5452369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54523692017-06-01 Matriptase zymogen supports epithelial development, homeostasis and regeneration Friis, Stine Tadeo, Daniel Le-Gall, Sylvain M. Jürgensen, Henrik Jessen Sales, Katiuchia Uzzun Camerer, Eric Bugge, Thomas H. BMC Biol Research Article BACKGROUND: Matriptase is a membrane serine protease essential for epithelial development, homeostasis, and regeneration, as well as a central orchestrator of pathogenic pericellular signaling in the context of inflammatory and proliferative diseases. Matriptase is an unusual protease in that its zymogen displays measurable enzymatic activity. RESULTS: Here, we used gain and loss of function genetics to investigate the possible biological functions of zymogen matriptase. Unexpectedly, transgenic mice mis-expressing a zymogen-locked version of matriptase in the epidermis displayed pathologies previously reported for transgenic mice mis-expressing wildtype epidermal matriptase. Equally surprising, mice engineered to express only zymogen-locked endogenous matriptase, unlike matriptase null mice, were viable, developed epithelial barrier function, and regenerated the injured epithelium. Compatible with these observations, wildtype and zymogen-locked matriptase were equipotent activators of PAR-2 inflammatory signaling. CONCLUSION: The study demonstrates that the matriptase zymogen is biologically active and is capable of executing developmental and homeostatic functions of the protease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-017-0384-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-01 /pmc/articles/PMC5452369/ /pubmed/28571576 http://dx.doi.org/10.1186/s12915-017-0384-4 Text en © Bugge et al. 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Friis, Stine Tadeo, Daniel Le-Gall, Sylvain M. Jürgensen, Henrik Jessen Sales, Katiuchia Uzzun Camerer, Eric Bugge, Thomas H. Matriptase zymogen supports epithelial development, homeostasis and regeneration |
title | Matriptase zymogen supports epithelial development, homeostasis and regeneration |
title_full | Matriptase zymogen supports epithelial development, homeostasis and regeneration |
title_fullStr | Matriptase zymogen supports epithelial development, homeostasis and regeneration |
title_full_unstemmed | Matriptase zymogen supports epithelial development, homeostasis and regeneration |
title_short | Matriptase zymogen supports epithelial development, homeostasis and regeneration |
title_sort | matriptase zymogen supports epithelial development, homeostasis and regeneration |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452369/ https://www.ncbi.nlm.nih.gov/pubmed/28571576 http://dx.doi.org/10.1186/s12915-017-0384-4 |
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