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The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss

Membrane-bound proteases are essential for epidermal integrity. Human airway trypsin-like protease 4 (HAT-L4) is a type II transmembrane serine protease. Currently, its biochemical property, cellular distribution and physiological function remain unknown. Here we examined HAT-L4 expression and funct...

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Autores principales: Zhang, Zhiwei, Hu, Yae, Yan, Ruhong, Dong, Liang, Jiang, Yizhi, Zhou, Zhichao, Liu, Meng, Zhou, Tiantian, Dong, Ningzheng, Wu, Qingyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364460/
https://www.ncbi.nlm.nih.gov/pubmed/28338078
http://dx.doi.org/10.1038/srep45262
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author Zhang, Zhiwei
Hu, Yae
Yan, Ruhong
Dong, Liang
Jiang, Yizhi
Zhou, Zhichao
Liu, Meng
Zhou, Tiantian
Dong, Ningzheng
Wu, Qingyu
author_facet Zhang, Zhiwei
Hu, Yae
Yan, Ruhong
Dong, Liang
Jiang, Yizhi
Zhou, Zhichao
Liu, Meng
Zhou, Tiantian
Dong, Ningzheng
Wu, Qingyu
author_sort Zhang, Zhiwei
collection PubMed
description Membrane-bound proteases are essential for epidermal integrity. Human airway trypsin-like protease 4 (HAT-L4) is a type II transmembrane serine protease. Currently, its biochemical property, cellular distribution and physiological function remain unknown. Here we examined HAT-L4 expression and function in vitro and in vivo. In Western analysis, HAT-L4 expressed in transfected CHO cells appeared as a 48-kDa protein. Flow cytometry confirmed HAT-L4 expression on the cell surface with the expected membrane topology. RT-PCR and immunostaining experiments indicated that HAT-L4 was expressed in epithelial cells and exocrine glands in tissues including skin, esophagus, trachea, tongue, eye, bladder, testis and uterus. In the skin, HAT-L4 expression was abundant in keratinocytes and sebaceous glands. We generated HAT-L4 knockout mice by disrupting the Tmprss11f gene encoding HAT-L4. HAT-L4 knockout mice were viable and fertile. No defects were found in HAT-L4 knockout mice in hair growth, wound healing, water repulsion and body temperature regulation. Compared with wild-type controls, HAT-L4-deficient newborn mice had greater body fluid loss and higher mortality in a trans-epidermal body fluid loss test. In metabolic studies, HAT-L4-deficient adult mice drank water more frequently than wild-type controls did. These results indicate that HAT-L4 is important in epidermal barrier function to prevent body fluid loss.
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spelling pubmed-53644602017-03-28 The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss Zhang, Zhiwei Hu, Yae Yan, Ruhong Dong, Liang Jiang, Yizhi Zhou, Zhichao Liu, Meng Zhou, Tiantian Dong, Ningzheng Wu, Qingyu Sci Rep Article Membrane-bound proteases are essential for epidermal integrity. Human airway trypsin-like protease 4 (HAT-L4) is a type II transmembrane serine protease. Currently, its biochemical property, cellular distribution and physiological function remain unknown. Here we examined HAT-L4 expression and function in vitro and in vivo. In Western analysis, HAT-L4 expressed in transfected CHO cells appeared as a 48-kDa protein. Flow cytometry confirmed HAT-L4 expression on the cell surface with the expected membrane topology. RT-PCR and immunostaining experiments indicated that HAT-L4 was expressed in epithelial cells and exocrine glands in tissues including skin, esophagus, trachea, tongue, eye, bladder, testis and uterus. In the skin, HAT-L4 expression was abundant in keratinocytes and sebaceous glands. We generated HAT-L4 knockout mice by disrupting the Tmprss11f gene encoding HAT-L4. HAT-L4 knockout mice were viable and fertile. No defects were found in HAT-L4 knockout mice in hair growth, wound healing, water repulsion and body temperature regulation. Compared with wild-type controls, HAT-L4-deficient newborn mice had greater body fluid loss and higher mortality in a trans-epidermal body fluid loss test. In metabolic studies, HAT-L4-deficient adult mice drank water more frequently than wild-type controls did. These results indicate that HAT-L4 is important in epidermal barrier function to prevent body fluid loss. Nature Publishing Group 2017-03-24 /pmc/articles/PMC5364460/ /pubmed/28338078 http://dx.doi.org/10.1038/srep45262 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhang, Zhiwei
Hu, Yae
Yan, Ruhong
Dong, Liang
Jiang, Yizhi
Zhou, Zhichao
Liu, Meng
Zhou, Tiantian
Dong, Ningzheng
Wu, Qingyu
The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
title The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
title_full The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
title_fullStr The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
title_full_unstemmed The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
title_short The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
title_sort transmembrane serine protease hat-like 4 is important for epidermal barrier function to prevent body fluid loss
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364460/
https://www.ncbi.nlm.nih.gov/pubmed/28338078
http://dx.doi.org/10.1038/srep45262
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