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ID1 and CEBPA coordinate epidermal progenitor cell differentiation
The regulatory circuits that coordinate epidermal differentiation during development are still not fully understood. Here, we report that the transcriptional regulator ID1 is enriched in mouse basal epidermal progenitor cells and find ID1 expression to be diminished upon differentiation. In utero si...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845743/ https://www.ncbi.nlm.nih.gov/pubmed/36330928 http://dx.doi.org/10.1242/dev.201262 |
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author | Kantzer, Christina Geraldine Yang, Wei Grommisch, David Patil, Kim Vikhe Mak, Kylie Hin-Man Shirokova, Vera Genander, Maria |
author_facet | Kantzer, Christina Geraldine Yang, Wei Grommisch, David Patil, Kim Vikhe Mak, Kylie Hin-Man Shirokova, Vera Genander, Maria |
author_sort | Kantzer, Christina Geraldine |
collection | PubMed |
description | The regulatory circuits that coordinate epidermal differentiation during development are still not fully understood. Here, we report that the transcriptional regulator ID1 is enriched in mouse basal epidermal progenitor cells and find ID1 expression to be diminished upon differentiation. In utero silencing of Id1 impairs progenitor cell proliferation, leads to precocious delamination of targeted progenitor cells and enables differentiated keratinocytes to retain progenitor markers and characteristics. Transcriptional profiling suggests that ID1 acts by mediating adhesion to the basement membrane while inhibiting spinous layer differentiation. Co-immunoprecipitation reveals ID1 binding to transcriptional regulators of the class I bHLH family. We localize bHLH Tcf3, Tcf4 and Tcf12 to epidermal progenitor cells during epidermal stratification and establish TCF3 as a downstream effector of ID1-mediated epidermal proliferation. Finally, we identify crosstalk between CEBPA, a known mediator of epidermal differentiation, and Id1, and demonstrate that CEBPA antagonizes BMP-induced activation of Id1. Our work establishes ID1 as a key coordinator of epidermal development, acting to balance progenitor proliferation with differentiation and unveils how functional crosstalk between CEBPA and Id1 orchestrates epidermal lineage progression. |
format | Online Article Text |
id | pubmed-9845743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-98457432023-01-27 ID1 and CEBPA coordinate epidermal progenitor cell differentiation Kantzer, Christina Geraldine Yang, Wei Grommisch, David Patil, Kim Vikhe Mak, Kylie Hin-Man Shirokova, Vera Genander, Maria Development Research Article The regulatory circuits that coordinate epidermal differentiation during development are still not fully understood. Here, we report that the transcriptional regulator ID1 is enriched in mouse basal epidermal progenitor cells and find ID1 expression to be diminished upon differentiation. In utero silencing of Id1 impairs progenitor cell proliferation, leads to precocious delamination of targeted progenitor cells and enables differentiated keratinocytes to retain progenitor markers and characteristics. Transcriptional profiling suggests that ID1 acts by mediating adhesion to the basement membrane while inhibiting spinous layer differentiation. Co-immunoprecipitation reveals ID1 binding to transcriptional regulators of the class I bHLH family. We localize bHLH Tcf3, Tcf4 and Tcf12 to epidermal progenitor cells during epidermal stratification and establish TCF3 as a downstream effector of ID1-mediated epidermal proliferation. Finally, we identify crosstalk between CEBPA, a known mediator of epidermal differentiation, and Id1, and demonstrate that CEBPA antagonizes BMP-induced activation of Id1. Our work establishes ID1 as a key coordinator of epidermal development, acting to balance progenitor proliferation with differentiation and unveils how functional crosstalk between CEBPA and Id1 orchestrates epidermal lineage progression. The Company of Biologists Ltd 2022-11-16 /pmc/articles/PMC9845743/ /pubmed/36330928 http://dx.doi.org/10.1242/dev.201262 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Kantzer, Christina Geraldine Yang, Wei Grommisch, David Patil, Kim Vikhe Mak, Kylie Hin-Man Shirokova, Vera Genander, Maria ID1 and CEBPA coordinate epidermal progenitor cell differentiation |
title | ID1 and CEBPA coordinate epidermal progenitor cell differentiation |
title_full | ID1 and CEBPA coordinate epidermal progenitor cell differentiation |
title_fullStr | ID1 and CEBPA coordinate epidermal progenitor cell differentiation |
title_full_unstemmed | ID1 and CEBPA coordinate epidermal progenitor cell differentiation |
title_short | ID1 and CEBPA coordinate epidermal progenitor cell differentiation |
title_sort | id1 and cebpa coordinate epidermal progenitor cell differentiation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845743/ https://www.ncbi.nlm.nih.gov/pubmed/36330928 http://dx.doi.org/10.1242/dev.201262 |
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