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Forkhead Box C1 Regulates Human Primary Keratinocyte Terminal Differentiation
The epidermis serves as a critical protective barrier between the internal and external environment of the human body. Its remarkable barrier function is established through the keratinocyte (KC) terminal differentiation program. The transcription factors specifically regulating terminal differentia...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132327/ https://www.ncbi.nlm.nih.gov/pubmed/27907090 http://dx.doi.org/10.1371/journal.pone.0167392 |
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author | Bin, Lianghua Deng, Liehua Yang, Hengwen Zhu, Leqing Wang, Xiao Edwards, Michael G. Richers, Brittany Leung, Donald Y. M. |
author_facet | Bin, Lianghua Deng, Liehua Yang, Hengwen Zhu, Leqing Wang, Xiao Edwards, Michael G. Richers, Brittany Leung, Donald Y. M. |
author_sort | Bin, Lianghua |
collection | PubMed |
description | The epidermis serves as a critical protective barrier between the internal and external environment of the human body. Its remarkable barrier function is established through the keratinocyte (KC) terminal differentiation program. The transcription factors specifically regulating terminal differentiation remain largely unknown. Using a RNA-sequencing (RNA-seq) profiling approach, we found that forkhead box c 1 (FOXC1) was significantly up-regulated in human normal primary KC during the course of differentiation. This observation was validated in human normal primary KC from several different donors and human skin biopsies. Silencing FOXC1 in human normal primary KC undergoing differentiation led to significant down-regulation of late terminal differentiation genes markers including epidermal differentiation complex genes, keratinization genes, sphingolipid/ceramide metabolic process genes and epidermal specific cell-cell adhesion genes. We further demonstrated that FOXC1 works down-stream of ZNF750 and KLF4, and upstream of GRHL3. Thus, this study defines FOXC1 as a regulator specific for KC terminal differentiation and establishes its potential position in the genetic regulatory network. |
format | Online Article Text |
id | pubmed-5132327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51323272016-12-21 Forkhead Box C1 Regulates Human Primary Keratinocyte Terminal Differentiation Bin, Lianghua Deng, Liehua Yang, Hengwen Zhu, Leqing Wang, Xiao Edwards, Michael G. Richers, Brittany Leung, Donald Y. M. PLoS One Research Article The epidermis serves as a critical protective barrier between the internal and external environment of the human body. Its remarkable barrier function is established through the keratinocyte (KC) terminal differentiation program. The transcription factors specifically regulating terminal differentiation remain largely unknown. Using a RNA-sequencing (RNA-seq) profiling approach, we found that forkhead box c 1 (FOXC1) was significantly up-regulated in human normal primary KC during the course of differentiation. This observation was validated in human normal primary KC from several different donors and human skin biopsies. Silencing FOXC1 in human normal primary KC undergoing differentiation led to significant down-regulation of late terminal differentiation genes markers including epidermal differentiation complex genes, keratinization genes, sphingolipid/ceramide metabolic process genes and epidermal specific cell-cell adhesion genes. We further demonstrated that FOXC1 works down-stream of ZNF750 and KLF4, and upstream of GRHL3. Thus, this study defines FOXC1 as a regulator specific for KC terminal differentiation and establishes its potential position in the genetic regulatory network. Public Library of Science 2016-12-01 /pmc/articles/PMC5132327/ /pubmed/27907090 http://dx.doi.org/10.1371/journal.pone.0167392 Text en © 2016 Bin 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 Bin, Lianghua Deng, Liehua Yang, Hengwen Zhu, Leqing Wang, Xiao Edwards, Michael G. Richers, Brittany Leung, Donald Y. M. Forkhead Box C1 Regulates Human Primary Keratinocyte Terminal Differentiation |
title | Forkhead Box C1 Regulates Human Primary Keratinocyte Terminal Differentiation |
title_full | Forkhead Box C1 Regulates Human Primary Keratinocyte Terminal Differentiation |
title_fullStr | Forkhead Box C1 Regulates Human Primary Keratinocyte Terminal Differentiation |
title_full_unstemmed | Forkhead Box C1 Regulates Human Primary Keratinocyte Terminal Differentiation |
title_short | Forkhead Box C1 Regulates Human Primary Keratinocyte Terminal Differentiation |
title_sort | forkhead box c1 regulates human primary keratinocyte terminal differentiation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132327/ https://www.ncbi.nlm.nih.gov/pubmed/27907090 http://dx.doi.org/10.1371/journal.pone.0167392 |
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