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TMEM45A Is Dispensable for Epidermal Morphogenesis, Keratinization and Barrier Formation

TMEM45A gene encodes an initially uncharacterized predicted transmembrane protein. We previously showed that this gene is highly expressed in keratinocytes where its expression correlates with keratinization, suggesting a role in normal epidermal physiology. To test this hypothesis, we generated TME...

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Autores principales: Hayez, Aurélie, Roegiers, Edith, Malaisse, Jérémy, Balau, Benoit, Sterpin, Christiane, Achouri, Younes, Lambert De Rouvroit, Catherine, Poumay, Yves, Michiels, Carine, De Backer, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718520/
https://www.ncbi.nlm.nih.gov/pubmed/26785122
http://dx.doi.org/10.1371/journal.pone.0147069
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author Hayez, Aurélie
Roegiers, Edith
Malaisse, Jérémy
Balau, Benoit
Sterpin, Christiane
Achouri, Younes
Lambert De Rouvroit, Catherine
Poumay, Yves
Michiels, Carine
De Backer, Olivier
author_facet Hayez, Aurélie
Roegiers, Edith
Malaisse, Jérémy
Balau, Benoit
Sterpin, Christiane
Achouri, Younes
Lambert De Rouvroit, Catherine
Poumay, Yves
Michiels, Carine
De Backer, Olivier
author_sort Hayez, Aurélie
collection PubMed
description TMEM45A gene encodes an initially uncharacterized predicted transmembrane protein. We previously showed that this gene is highly expressed in keratinocytes where its expression correlates with keratinization, suggesting a role in normal epidermal physiology. To test this hypothesis, we generated TMEM45A knockout mice and found that these mice develop without any evident phenotype. The morphology of the epidermis assessed by histology and by labelling differentiation markers in immunofluorescence was not altered. Toluidine blue permeability assay showed that the epidermal barrier develops normally during embryonic development. We also showed that depletion of TMEM45A in human keratinocytes does not alter their potential to form in vitro 3D-reconstructed epidermis. Indeed, epidermis with normal morphogenesis were generated from TMEM45A-silenced keratinocytes. Their expression of differentiation markers quantified by RT-qPCR and evidenced by immunofluorescence labelling as well as their barrier function estimated by Lucifer yellow permeability were similar to the control epidermis. In summary, TMEM45A gene expression is dispensable for epidermal morphogenesis, keratinization and barrier formation. If this protein plays a role in the epidermis, its experimental depletion can possibly be compensated by other proteins in the two experimental models analyzed in this study.
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spelling pubmed-47185202016-01-30 TMEM45A Is Dispensable for Epidermal Morphogenesis, Keratinization and Barrier Formation Hayez, Aurélie Roegiers, Edith Malaisse, Jérémy Balau, Benoit Sterpin, Christiane Achouri, Younes Lambert De Rouvroit, Catherine Poumay, Yves Michiels, Carine De Backer, Olivier PLoS One Research Article TMEM45A gene encodes an initially uncharacterized predicted transmembrane protein. We previously showed that this gene is highly expressed in keratinocytes where its expression correlates with keratinization, suggesting a role in normal epidermal physiology. To test this hypothesis, we generated TMEM45A knockout mice and found that these mice develop without any evident phenotype. The morphology of the epidermis assessed by histology and by labelling differentiation markers in immunofluorescence was not altered. Toluidine blue permeability assay showed that the epidermal barrier develops normally during embryonic development. We also showed that depletion of TMEM45A in human keratinocytes does not alter their potential to form in vitro 3D-reconstructed epidermis. Indeed, epidermis with normal morphogenesis were generated from TMEM45A-silenced keratinocytes. Their expression of differentiation markers quantified by RT-qPCR and evidenced by immunofluorescence labelling as well as their barrier function estimated by Lucifer yellow permeability were similar to the control epidermis. In summary, TMEM45A gene expression is dispensable for epidermal morphogenesis, keratinization and barrier formation. If this protein plays a role in the epidermis, its experimental depletion can possibly be compensated by other proteins in the two experimental models analyzed in this study. Public Library of Science 2016-01-19 /pmc/articles/PMC4718520/ /pubmed/26785122 http://dx.doi.org/10.1371/journal.pone.0147069 Text en © 2016 Hayez et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hayez, Aurélie
Roegiers, Edith
Malaisse, Jérémy
Balau, Benoit
Sterpin, Christiane
Achouri, Younes
Lambert De Rouvroit, Catherine
Poumay, Yves
Michiels, Carine
De Backer, Olivier
TMEM45A Is Dispensable for Epidermal Morphogenesis, Keratinization and Barrier Formation
title TMEM45A Is Dispensable for Epidermal Morphogenesis, Keratinization and Barrier Formation
title_full TMEM45A Is Dispensable for Epidermal Morphogenesis, Keratinization and Barrier Formation
title_fullStr TMEM45A Is Dispensable for Epidermal Morphogenesis, Keratinization and Barrier Formation
title_full_unstemmed TMEM45A Is Dispensable for Epidermal Morphogenesis, Keratinization and Barrier Formation
title_short TMEM45A Is Dispensable for Epidermal Morphogenesis, Keratinization and Barrier Formation
title_sort tmem45a is dispensable for epidermal morphogenesis, keratinization and barrier formation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718520/
https://www.ncbi.nlm.nih.gov/pubmed/26785122
http://dx.doi.org/10.1371/journal.pone.0147069
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