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Nfatc1’s Role in Mammary Epithelial Morphogenesis and Basal Stem/progenitor Cell Self-renewal

Mammary gland is an outstanding system to study the regulatory mechanisms governing adult epithelial stem cell activity. Stem cells in the basal layer of the mammary gland fuel the morphogenesis and regeneration of a complex epithelial network during development and upon transplantation. The self-re...

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Autores principales: McNeil, Melissa, Han, Yingying, Sun, Peng, Watanabe, Kazuhide, Jiang, Jun, Chen, Natasha, Yu, Zhengquan, Zhou, Bin, Dai, Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858291/
https://www.ncbi.nlm.nih.gov/pubmed/34932179
http://dx.doi.org/10.1007/s10911-021-09502-6
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author McNeil, Melissa
Han, Yingying
Sun, Peng
Watanabe, Kazuhide
Jiang, Jun
Chen, Natasha
Yu, Zhengquan
Zhou, Bin
Dai, Xing
author_facet McNeil, Melissa
Han, Yingying
Sun, Peng
Watanabe, Kazuhide
Jiang, Jun
Chen, Natasha
Yu, Zhengquan
Zhou, Bin
Dai, Xing
author_sort McNeil, Melissa
collection PubMed
description Mammary gland is an outstanding system to study the regulatory mechanisms governing adult epithelial stem cell activity. Stem cells in the basal layer of the mammary gland fuel the morphogenesis and regeneration of a complex epithelial network during development and upon transplantation. The self-renewal of basal stem/progenitor cells is subjected to regulation by both cell-intrinsic and extrinsic mechanisms. Nfatc1 is a transcription factor that regulates breast tumorigenesis and metastasis, but its role in mammary epithelial development and stem cell function has not been investigated. Here we show that Nfatc1 is expressed in a small subset of mammary basal epithelial cells and its epithelial-specific deletion results in mild defects in side branching and basal-luminal cell balance. Moreover, Nfatc1-deficient basal cells exhibit reduced colony forming ability in vitro and somewhat compromised regenerative potential upon transplantation. Thus, our study provides evidence for a detectable yet non-essential role of Nfatc1 in mammary epithelial morphogenesis and basal stem/progenitor cell self-renewal. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10911-021-09502-6.
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spelling pubmed-88582912022-02-23 Nfatc1’s Role in Mammary Epithelial Morphogenesis and Basal Stem/progenitor Cell Self-renewal McNeil, Melissa Han, Yingying Sun, Peng Watanabe, Kazuhide Jiang, Jun Chen, Natasha Yu, Zhengquan Zhou, Bin Dai, Xing J Mammary Gland Biol Neoplasia Original Paper Mammary gland is an outstanding system to study the regulatory mechanisms governing adult epithelial stem cell activity. Stem cells in the basal layer of the mammary gland fuel the morphogenesis and regeneration of a complex epithelial network during development and upon transplantation. The self-renewal of basal stem/progenitor cells is subjected to regulation by both cell-intrinsic and extrinsic mechanisms. Nfatc1 is a transcription factor that regulates breast tumorigenesis and metastasis, but its role in mammary epithelial development and stem cell function has not been investigated. Here we show that Nfatc1 is expressed in a small subset of mammary basal epithelial cells and its epithelial-specific deletion results in mild defects in side branching and basal-luminal cell balance. Moreover, Nfatc1-deficient basal cells exhibit reduced colony forming ability in vitro and somewhat compromised regenerative potential upon transplantation. Thus, our study provides evidence for a detectable yet non-essential role of Nfatc1 in mammary epithelial morphogenesis and basal stem/progenitor cell self-renewal. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10911-021-09502-6. Springer US 2021-12-21 2021 /pmc/articles/PMC8858291/ /pubmed/34932179 http://dx.doi.org/10.1007/s10911-021-09502-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
McNeil, Melissa
Han, Yingying
Sun, Peng
Watanabe, Kazuhide
Jiang, Jun
Chen, Natasha
Yu, Zhengquan
Zhou, Bin
Dai, Xing
Nfatc1’s Role in Mammary Epithelial Morphogenesis and Basal Stem/progenitor Cell Self-renewal
title Nfatc1’s Role in Mammary Epithelial Morphogenesis and Basal Stem/progenitor Cell Self-renewal
title_full Nfatc1’s Role in Mammary Epithelial Morphogenesis and Basal Stem/progenitor Cell Self-renewal
title_fullStr Nfatc1’s Role in Mammary Epithelial Morphogenesis and Basal Stem/progenitor Cell Self-renewal
title_full_unstemmed Nfatc1’s Role in Mammary Epithelial Morphogenesis and Basal Stem/progenitor Cell Self-renewal
title_short Nfatc1’s Role in Mammary Epithelial Morphogenesis and Basal Stem/progenitor Cell Self-renewal
title_sort nfatc1’s role in mammary epithelial morphogenesis and basal stem/progenitor cell self-renewal
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858291/
https://www.ncbi.nlm.nih.gov/pubmed/34932179
http://dx.doi.org/10.1007/s10911-021-09502-6
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