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The miR‐200 family is required for ectodermal organ development through the regulation of the epithelial stem cell niche

The murine lower incisor ectodermal organ contains a single epithelial stem cell (SC) niche that provides epithelial progenitor cells to the continuously growing rodent incisor. The dental stem cell niche gives rise to several cell types and we demonstrate that the miR‐200 family regulates these cel...

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Autores principales: Sweat, Mason, Sweat, Yan, Yu, Wenjie, Su, Dan, Leonard, Riley J., Eliason, Steven L., Amendt, Brad A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247948/
https://www.ncbi.nlm.nih.gov/pubmed/33529466
http://dx.doi.org/10.1002/stem.3342
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author Sweat, Mason
Sweat, Yan
Yu, Wenjie
Su, Dan
Leonard, Riley J.
Eliason, Steven L.
Amendt, Brad A.
author_facet Sweat, Mason
Sweat, Yan
Yu, Wenjie
Su, Dan
Leonard, Riley J.
Eliason, Steven L.
Amendt, Brad A.
author_sort Sweat, Mason
collection PubMed
description The murine lower incisor ectodermal organ contains a single epithelial stem cell (SC) niche that provides epithelial progenitor cells to the continuously growing rodent incisor. The dental stem cell niche gives rise to several cell types and we demonstrate that the miR‐200 family regulates these cell fates. The miR‐200 family is highly enriched in the differentiated dental epithelium and absent in the stem cell niche. In this study, we inhibited the miR‐200 family in developing murine embryos using new technology, resulting in an expanded epithelial stem cell niche and lack of cell differentiation. Inhibition of individual miRs within the miR‐200 cluster resulted in differential developmental and cell morphology defects. miR‐200 inhibition increased the expression of dental epithelial stem cell markers, expanded the stem cell niche and decreased progenitor cell differentiation. RNA‐seq. identified miR‐200 regulatory pathways involved in cell differentiation and compartmentalization of the stem cell niche. The miR‐200 family regulates signaling pathways required for cell differentiation and cell cycle progression. The inhibition of miR‐200 decreased the size of the lower incisor due to increased autophagy and cell death. New miR‐200 targets demonstrate gene networks and pathways controlling cell differentiation and maintenance of the stem cell niche. This is the first report demonstrating how the miR‐200 family is required for in vivo progenitor cell proliferation and differentiation.
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spelling pubmed-82479482021-07-02 The miR‐200 family is required for ectodermal organ development through the regulation of the epithelial stem cell niche Sweat, Mason Sweat, Yan Yu, Wenjie Su, Dan Leonard, Riley J. Eliason, Steven L. Amendt, Brad A. Stem Cells Tissue‐specific Stem Cells The murine lower incisor ectodermal organ contains a single epithelial stem cell (SC) niche that provides epithelial progenitor cells to the continuously growing rodent incisor. The dental stem cell niche gives rise to several cell types and we demonstrate that the miR‐200 family regulates these cell fates. The miR‐200 family is highly enriched in the differentiated dental epithelium and absent in the stem cell niche. In this study, we inhibited the miR‐200 family in developing murine embryos using new technology, resulting in an expanded epithelial stem cell niche and lack of cell differentiation. Inhibition of individual miRs within the miR‐200 cluster resulted in differential developmental and cell morphology defects. miR‐200 inhibition increased the expression of dental epithelial stem cell markers, expanded the stem cell niche and decreased progenitor cell differentiation. RNA‐seq. identified miR‐200 regulatory pathways involved in cell differentiation and compartmentalization of the stem cell niche. The miR‐200 family regulates signaling pathways required for cell differentiation and cell cycle progression. The inhibition of miR‐200 decreased the size of the lower incisor due to increased autophagy and cell death. New miR‐200 targets demonstrate gene networks and pathways controlling cell differentiation and maintenance of the stem cell niche. This is the first report demonstrating how the miR‐200 family is required for in vivo progenitor cell proliferation and differentiation. John Wiley & Sons, Inc. 2021-02-13 2021-06 /pmc/articles/PMC8247948/ /pubmed/33529466 http://dx.doi.org/10.1002/stem.3342 Text en © 2021 The Authors. stem cells published by Wiley Periodicals LLC on behalf of AlphaMed Press 2021 https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Tissue‐specific Stem Cells
Sweat, Mason
Sweat, Yan
Yu, Wenjie
Su, Dan
Leonard, Riley J.
Eliason, Steven L.
Amendt, Brad A.
The miR‐200 family is required for ectodermal organ development through the regulation of the epithelial stem cell niche
title The miR‐200 family is required for ectodermal organ development through the regulation of the epithelial stem cell niche
title_full The miR‐200 family is required for ectodermal organ development through the regulation of the epithelial stem cell niche
title_fullStr The miR‐200 family is required for ectodermal organ development through the regulation of the epithelial stem cell niche
title_full_unstemmed The miR‐200 family is required for ectodermal organ development through the regulation of the epithelial stem cell niche
title_short The miR‐200 family is required for ectodermal organ development through the regulation of the epithelial stem cell niche
title_sort mir‐200 family is required for ectodermal organ development through the regulation of the epithelial stem cell niche
topic Tissue‐specific Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247948/
https://www.ncbi.nlm.nih.gov/pubmed/33529466
http://dx.doi.org/10.1002/stem.3342
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