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Single-cell lineage tracing in the mammary gland reveals stochastic clonal dispersion of stem/progenitor cell progeny

The mammary gland undergoes cycles of growth and regeneration throughout reproductive life, a process that requires mammary stem cells (MaSCs). Whilst recent genetic fate-mapping studies using lineage-specific promoters have provided valuable insights into the mammary epithelial hierarchy, the true...

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Autores principales: Davis, Felicity M., Lloyd-Lewis, Bethan, Harris, Olivia B., Kozar, Sarah, Winton, Douglas J., Muresan, Leila, Watson, Christine J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093309/
https://www.ncbi.nlm.nih.gov/pubmed/27779190
http://dx.doi.org/10.1038/ncomms13053
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author Davis, Felicity M.
Lloyd-Lewis, Bethan
Harris, Olivia B.
Kozar, Sarah
Winton, Douglas J.
Muresan, Leila
Watson, Christine J.
author_facet Davis, Felicity M.
Lloyd-Lewis, Bethan
Harris, Olivia B.
Kozar, Sarah
Winton, Douglas J.
Muresan, Leila
Watson, Christine J.
author_sort Davis, Felicity M.
collection PubMed
description The mammary gland undergoes cycles of growth and regeneration throughout reproductive life, a process that requires mammary stem cells (MaSCs). Whilst recent genetic fate-mapping studies using lineage-specific promoters have provided valuable insights into the mammary epithelial hierarchy, the true differentiation potential of adult MaSCs remains unclear. To address this, herein we utilize a stochastic genetic-labelling strategy to indelibly mark a single cell and its progeny in situ, combined with tissue clearing and 3D imaging. Using this approach, clones arising from a single parent cell could be visualized in their entirety. We reveal that clonal progeny contribute exclusively to either luminal or basal lineages and are distributed sporadically to branching ducts or alveoli. Quantitative analyses suggest that pools of unipotent stem/progenitor cells contribute to adult mammary gland development. Our results highlight the utility of tracing a single cell and reveal that progeny of a single proliferative MaSC/progenitor are dispersed throughout the epithelium.
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spelling pubmed-50933092016-11-18 Single-cell lineage tracing in the mammary gland reveals stochastic clonal dispersion of stem/progenitor cell progeny Davis, Felicity M. Lloyd-Lewis, Bethan Harris, Olivia B. Kozar, Sarah Winton, Douglas J. Muresan, Leila Watson, Christine J. Nat Commun Article The mammary gland undergoes cycles of growth and regeneration throughout reproductive life, a process that requires mammary stem cells (MaSCs). Whilst recent genetic fate-mapping studies using lineage-specific promoters have provided valuable insights into the mammary epithelial hierarchy, the true differentiation potential of adult MaSCs remains unclear. To address this, herein we utilize a stochastic genetic-labelling strategy to indelibly mark a single cell and its progeny in situ, combined with tissue clearing and 3D imaging. Using this approach, clones arising from a single parent cell could be visualized in their entirety. We reveal that clonal progeny contribute exclusively to either luminal or basal lineages and are distributed sporadically to branching ducts or alveoli. Quantitative analyses suggest that pools of unipotent stem/progenitor cells contribute to adult mammary gland development. Our results highlight the utility of tracing a single cell and reveal that progeny of a single proliferative MaSC/progenitor are dispersed throughout the epithelium. Nature Publishing Group 2016-10-25 /pmc/articles/PMC5093309/ /pubmed/27779190 http://dx.doi.org/10.1038/ncomms13053 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Davis, Felicity M.
Lloyd-Lewis, Bethan
Harris, Olivia B.
Kozar, Sarah
Winton, Douglas J.
Muresan, Leila
Watson, Christine J.
Single-cell lineage tracing in the mammary gland reveals stochastic clonal dispersion of stem/progenitor cell progeny
title Single-cell lineage tracing in the mammary gland reveals stochastic clonal dispersion of stem/progenitor cell progeny
title_full Single-cell lineage tracing in the mammary gland reveals stochastic clonal dispersion of stem/progenitor cell progeny
title_fullStr Single-cell lineage tracing in the mammary gland reveals stochastic clonal dispersion of stem/progenitor cell progeny
title_full_unstemmed Single-cell lineage tracing in the mammary gland reveals stochastic clonal dispersion of stem/progenitor cell progeny
title_short Single-cell lineage tracing in the mammary gland reveals stochastic clonal dispersion of stem/progenitor cell progeny
title_sort single-cell lineage tracing in the mammary gland reveals stochastic clonal dispersion of stem/progenitor cell progeny
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093309/
https://www.ncbi.nlm.nih.gov/pubmed/27779190
http://dx.doi.org/10.1038/ncomms13053
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