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Anatomical localization of progenitor cells in human breast tissue reveals enrichment of uncommitted cells within immature lobules

INTRODUCTION: Lineage tracing studies in mice have revealed the localization and existence of lineage-restricted mammary epithelial progenitor cells that functionally contribute to expansive growth during puberty and differentiation during pregnancy. However, extensive anatomical differences between...

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Autores principales: Arendt, Lisa M, Keller, Patricia J, Skibinski, Adam, Goncalves, Kevin, Naber, Stephen P, Buchsbaum, Rachel J, Gilmore, Hannah, Come, Steven E, Kuperwasser, Charlotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303132/
https://www.ncbi.nlm.nih.gov/pubmed/25315014
http://dx.doi.org/10.1186/s13058-014-0453-3
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author Arendt, Lisa M
Keller, Patricia J
Skibinski, Adam
Goncalves, Kevin
Naber, Stephen P
Buchsbaum, Rachel J
Gilmore, Hannah
Come, Steven E
Kuperwasser, Charlotte
author_facet Arendt, Lisa M
Keller, Patricia J
Skibinski, Adam
Goncalves, Kevin
Naber, Stephen P
Buchsbaum, Rachel J
Gilmore, Hannah
Come, Steven E
Kuperwasser, Charlotte
author_sort Arendt, Lisa M
collection PubMed
description INTRODUCTION: Lineage tracing studies in mice have revealed the localization and existence of lineage-restricted mammary epithelial progenitor cells that functionally contribute to expansive growth during puberty and differentiation during pregnancy. However, extensive anatomical differences between mouse and human mammary tissues preclude the direct translation of rodent findings to the human breast. Therefore, here we characterize the mammary progenitor cell hierarchy and identify the anatomic location of progenitor cells within human breast tissues. METHODS: Mammary epithelial cells (MECs) were isolated from disease-free reduction mammoplasty tissues and assayed for stem/progenitor activity in vitro and in vivo. MECs were sorted and evaluated for growth on collagen and expression of lineages markers. Breast lobules were microdissected and individually characterized based on lineage markers and steroid receptor expression to identify the anatomic location of progenitor cells. Spanning-tree progression analysis of density-normalized events (SPADE) was used to identify the cellular hierarchy of MECs within lobules from high-dimensional cytometry data. RESULTS: Integrating multiple assays for progenitor activity, we identified the presence of luminal alveolar and basal ductal progenitors. Further, we show that Type I lobules of the human breast were the least mature, demonstrating an unrestricted pattern of expression of luminal and basal lineage markers. Consistent with this, SPADE analysis revealed that immature lobules were enriched for basal progenitor cells, while mature lobules consisted of increased hierarchal complexity of cells within the luminal lineages. CONCLUSIONS: These results reveal underlying differences in the human breast epithelial hierarchy and suggest that with increasing glandular maturity, the epithelial hierarchy also becomes more complex. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-014-0453-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-43031322015-01-23 Anatomical localization of progenitor cells in human breast tissue reveals enrichment of uncommitted cells within immature lobules Arendt, Lisa M Keller, Patricia J Skibinski, Adam Goncalves, Kevin Naber, Stephen P Buchsbaum, Rachel J Gilmore, Hannah Come, Steven E Kuperwasser, Charlotte Breast Cancer Res Research Article INTRODUCTION: Lineage tracing studies in mice have revealed the localization and existence of lineage-restricted mammary epithelial progenitor cells that functionally contribute to expansive growth during puberty and differentiation during pregnancy. However, extensive anatomical differences between mouse and human mammary tissues preclude the direct translation of rodent findings to the human breast. Therefore, here we characterize the mammary progenitor cell hierarchy and identify the anatomic location of progenitor cells within human breast tissues. METHODS: Mammary epithelial cells (MECs) were isolated from disease-free reduction mammoplasty tissues and assayed for stem/progenitor activity in vitro and in vivo. MECs were sorted and evaluated for growth on collagen and expression of lineages markers. Breast lobules were microdissected and individually characterized based on lineage markers and steroid receptor expression to identify the anatomic location of progenitor cells. Spanning-tree progression analysis of density-normalized events (SPADE) was used to identify the cellular hierarchy of MECs within lobules from high-dimensional cytometry data. RESULTS: Integrating multiple assays for progenitor activity, we identified the presence of luminal alveolar and basal ductal progenitors. Further, we show that Type I lobules of the human breast were the least mature, demonstrating an unrestricted pattern of expression of luminal and basal lineage markers. Consistent with this, SPADE analysis revealed that immature lobules were enriched for basal progenitor cells, while mature lobules consisted of increased hierarchal complexity of cells within the luminal lineages. CONCLUSIONS: These results reveal underlying differences in the human breast epithelial hierarchy and suggest that with increasing glandular maturity, the epithelial hierarchy also becomes more complex. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-014-0453-3) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-15 2014 /pmc/articles/PMC4303132/ /pubmed/25315014 http://dx.doi.org/10.1186/s13058-014-0453-3 Text en © Arendt et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Arendt, Lisa M
Keller, Patricia J
Skibinski, Adam
Goncalves, Kevin
Naber, Stephen P
Buchsbaum, Rachel J
Gilmore, Hannah
Come, Steven E
Kuperwasser, Charlotte
Anatomical localization of progenitor cells in human breast tissue reveals enrichment of uncommitted cells within immature lobules
title Anatomical localization of progenitor cells in human breast tissue reveals enrichment of uncommitted cells within immature lobules
title_full Anatomical localization of progenitor cells in human breast tissue reveals enrichment of uncommitted cells within immature lobules
title_fullStr Anatomical localization of progenitor cells in human breast tissue reveals enrichment of uncommitted cells within immature lobules
title_full_unstemmed Anatomical localization of progenitor cells in human breast tissue reveals enrichment of uncommitted cells within immature lobules
title_short Anatomical localization of progenitor cells in human breast tissue reveals enrichment of uncommitted cells within immature lobules
title_sort anatomical localization of progenitor cells in human breast tissue reveals enrichment of uncommitted cells within immature lobules
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303132/
https://www.ncbi.nlm.nih.gov/pubmed/25315014
http://dx.doi.org/10.1186/s13058-014-0453-3
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