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Rab25 Deficiency Perturbs Epidermal Differentiation and Skin Barrier Function in Mice
Rab25, a member of the Rab11 small GTPase family, is central to achieving cellular polarity in epithelial tissues. Rab25 is highly expressed in epithelial cells of various tissues including breast, vagina, cervix, the gastrointestinal tract, and skin. Rab25 plays key roles in tumorigenesis, mainly b...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Applied Pharmacology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824620/ https://www.ncbi.nlm.nih.gov/pubmed/31564077 http://dx.doi.org/10.4062/biomolther.2019.125 |
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author | Jeong, Haengdueng Lim, Kyung-Min Goldenring, James R. Nam, Ki Taek |
author_facet | Jeong, Haengdueng Lim, Kyung-Min Goldenring, James R. Nam, Ki Taek |
author_sort | Jeong, Haengdueng |
collection | PubMed |
description | Rab25, a member of the Rab11 small GTPase family, is central to achieving cellular polarity in epithelial tissues. Rab25 is highly expressed in epithelial cells of various tissues including breast, vagina, cervix, the gastrointestinal tract, and skin. Rab25 plays key roles in tumorigenesis, mainly by regulating epithelial differentiation and proliferation. However, its role in skin physiology is relatively unknown. In this study, we demonstrated that Rab25 knock-out (KO) mice show a skin barrier dysfunction with high trans-epidermal water loss and low cutaneous hydration. To examine this observation, we investigated the histology and epidermal differentiation markers of the skin in Rab25 KO mice. Rab25 KO increased cell proliferation at the basal layer of epidermis, whereas the supra-basal layer remained unaffected. Ceramide, which is a critical lipid component for skin barrier function, was not altered by Rab25 KO in its distribution or amount, as determined by immunohistochemistry. Notably, levels of epidermal differentiation markers, including loricrin, involucrin, and keratins (5, 14, 1, and 10) increased prominently in Rab25 KO mice. In line with this, depletion of Rab25 with single hairpin RNA increased the expression of differentiation markers in a human keratinocyte cell line, HaCaT. Transcriptomic analysis of the skin revealed increased expression of genes associated with skin development, epidermal development, and keratinocyte differentiation in Rab25 KO mice. Collectively, these results suggested that Rab25 is involved in the regulation of epidermal differentiation and proliferation. |
format | Online Article Text |
id | pubmed-6824620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Korean Society of Applied Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-68246202019-11-04 Rab25 Deficiency Perturbs Epidermal Differentiation and Skin Barrier Function in Mice Jeong, Haengdueng Lim, Kyung-Min Goldenring, James R. Nam, Ki Taek Biomol Ther (Seoul) Original Article Rab25, a member of the Rab11 small GTPase family, is central to achieving cellular polarity in epithelial tissues. Rab25 is highly expressed in epithelial cells of various tissues including breast, vagina, cervix, the gastrointestinal tract, and skin. Rab25 plays key roles in tumorigenesis, mainly by regulating epithelial differentiation and proliferation. However, its role in skin physiology is relatively unknown. In this study, we demonstrated that Rab25 knock-out (KO) mice show a skin barrier dysfunction with high trans-epidermal water loss and low cutaneous hydration. To examine this observation, we investigated the histology and epidermal differentiation markers of the skin in Rab25 KO mice. Rab25 KO increased cell proliferation at the basal layer of epidermis, whereas the supra-basal layer remained unaffected. Ceramide, which is a critical lipid component for skin barrier function, was not altered by Rab25 KO in its distribution or amount, as determined by immunohistochemistry. Notably, levels of epidermal differentiation markers, including loricrin, involucrin, and keratins (5, 14, 1, and 10) increased prominently in Rab25 KO mice. In line with this, depletion of Rab25 with single hairpin RNA increased the expression of differentiation markers in a human keratinocyte cell line, HaCaT. Transcriptomic analysis of the skin revealed increased expression of genes associated with skin development, epidermal development, and keratinocyte differentiation in Rab25 KO mice. Collectively, these results suggested that Rab25 is involved in the regulation of epidermal differentiation and proliferation. The Korean Society of Applied Pharmacology 2019-11 2019-09-30 /pmc/articles/PMC6824620/ /pubmed/31564077 http://dx.doi.org/10.4062/biomolther.2019.125 Text en Copyright ©2019, The Korean Society of Applied Pharmacology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jeong, Haengdueng Lim, Kyung-Min Goldenring, James R. Nam, Ki Taek Rab25 Deficiency Perturbs Epidermal Differentiation and Skin Barrier Function in Mice |
title | Rab25 Deficiency Perturbs Epidermal Differentiation and Skin Barrier Function in Mice |
title_full | Rab25 Deficiency Perturbs Epidermal Differentiation and Skin Barrier Function in Mice |
title_fullStr | Rab25 Deficiency Perturbs Epidermal Differentiation and Skin Barrier Function in Mice |
title_full_unstemmed | Rab25 Deficiency Perturbs Epidermal Differentiation and Skin Barrier Function in Mice |
title_short | Rab25 Deficiency Perturbs Epidermal Differentiation and Skin Barrier Function in Mice |
title_sort | rab25 deficiency perturbs epidermal differentiation and skin barrier function in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824620/ https://www.ncbi.nlm.nih.gov/pubmed/31564077 http://dx.doi.org/10.4062/biomolther.2019.125 |
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