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Evidence of two distinct functionally specialized fibroblast lineages in breast stroma

BACKGROUND: The terminal duct lobular unit (TDLU) is the most dynamic structure in the human breast and the putative site of origin of human breast cancer. Although stromal cells contribute to a specialized microenvironment in many organs, this component remains largely understudied in the human bre...

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Autores principales: Morsing, Mikkel, Klitgaard, Marie Christine, Jafari, Abbas, Villadsen, René, Kassem, Moustapha, Petersen, Ole William, Rønnov-Jessen, Lone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093959/
https://www.ncbi.nlm.nih.gov/pubmed/27809866
http://dx.doi.org/10.1186/s13058-016-0769-2
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author Morsing, Mikkel
Klitgaard, Marie Christine
Jafari, Abbas
Villadsen, René
Kassem, Moustapha
Petersen, Ole William
Rønnov-Jessen, Lone
author_facet Morsing, Mikkel
Klitgaard, Marie Christine
Jafari, Abbas
Villadsen, René
Kassem, Moustapha
Petersen, Ole William
Rønnov-Jessen, Lone
author_sort Morsing, Mikkel
collection PubMed
description BACKGROUND: The terminal duct lobular unit (TDLU) is the most dynamic structure in the human breast and the putative site of origin of human breast cancer. Although stromal cells contribute to a specialized microenvironment in many organs, this component remains largely understudied in the human breast. We here demonstrate the impact on epithelium of two lineages of breast stromal fibroblasts, one of which accumulates in the TDLU while the other resides outside the TDLU in the interlobular stroma. METHODS: The two lineages are prospectively isolated by fluorescence activated cell sorting (FACS) based on different expression levels of CD105 and CD26. The characteristics of the two fibroblast lineages are assessed by immunocytochemical staining and gene expression analysis. The differentiation capacity of the two fibroblast populations is determined by exposure to specific differentiating conditions followed by analysis of adipogenic and osteogenic differentiation. To test whether the two fibroblast lineages are functionally imprinted by their site of origin, single cell sorted CD271(low)/MUC1(high) normal breast luminal epithelial cells are plated on fibroblast feeders for the observation of morphological development. Epithelial structure formation and polarization is shown by immunofluorescence and digitalized quantification of immunoperoxidase-stained cultures. RESULTS: Lobular fibroblasts are CD105(high)/CD26(low) while interlobular fibroblasts are CD105(low)/CD26(high). Once isolated the two lineages remain phenotypically stable and functionally distinct in culture. Lobular fibroblasts have properties in common with bone marrow derived mesenchymal stem cells and they specifically convey growth and branching morphogenesis of epithelial progenitors. CONCLUSIONS: Two distinct functionally specialized fibroblast lineages exist in the normal human breast, of which the lobular fibroblasts have properties in common with mesenchymal stem cells and support epithelial growth and morphogenesis. We propose that lobular fibroblasts constitute a specialized microenvironment for human breast luminal epithelial progenitors, i.e. the putative precursors of breast cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-016-0769-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-50939592016-11-07 Evidence of two distinct functionally specialized fibroblast lineages in breast stroma Morsing, Mikkel Klitgaard, Marie Christine Jafari, Abbas Villadsen, René Kassem, Moustapha Petersen, Ole William Rønnov-Jessen, Lone Breast Cancer Res Research Article BACKGROUND: The terminal duct lobular unit (TDLU) is the most dynamic structure in the human breast and the putative site of origin of human breast cancer. Although stromal cells contribute to a specialized microenvironment in many organs, this component remains largely understudied in the human breast. We here demonstrate the impact on epithelium of two lineages of breast stromal fibroblasts, one of which accumulates in the TDLU while the other resides outside the TDLU in the interlobular stroma. METHODS: The two lineages are prospectively isolated by fluorescence activated cell sorting (FACS) based on different expression levels of CD105 and CD26. The characteristics of the two fibroblast lineages are assessed by immunocytochemical staining and gene expression analysis. The differentiation capacity of the two fibroblast populations is determined by exposure to specific differentiating conditions followed by analysis of adipogenic and osteogenic differentiation. To test whether the two fibroblast lineages are functionally imprinted by their site of origin, single cell sorted CD271(low)/MUC1(high) normal breast luminal epithelial cells are plated on fibroblast feeders for the observation of morphological development. Epithelial structure formation and polarization is shown by immunofluorescence and digitalized quantification of immunoperoxidase-stained cultures. RESULTS: Lobular fibroblasts are CD105(high)/CD26(low) while interlobular fibroblasts are CD105(low)/CD26(high). Once isolated the two lineages remain phenotypically stable and functionally distinct in culture. Lobular fibroblasts have properties in common with bone marrow derived mesenchymal stem cells and they specifically convey growth and branching morphogenesis of epithelial progenitors. CONCLUSIONS: Two distinct functionally specialized fibroblast lineages exist in the normal human breast, of which the lobular fibroblasts have properties in common with mesenchymal stem cells and support epithelial growth and morphogenesis. We propose that lobular fibroblasts constitute a specialized microenvironment for human breast luminal epithelial progenitors, i.e. the putative precursors of breast cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-016-0769-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-03 2016 /pmc/articles/PMC5093959/ /pubmed/27809866 http://dx.doi.org/10.1186/s13058-016-0769-2 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Morsing, Mikkel
Klitgaard, Marie Christine
Jafari, Abbas
Villadsen, René
Kassem, Moustapha
Petersen, Ole William
Rønnov-Jessen, Lone
Evidence of two distinct functionally specialized fibroblast lineages in breast stroma
title Evidence of two distinct functionally specialized fibroblast lineages in breast stroma
title_full Evidence of two distinct functionally specialized fibroblast lineages in breast stroma
title_fullStr Evidence of two distinct functionally specialized fibroblast lineages in breast stroma
title_full_unstemmed Evidence of two distinct functionally specialized fibroblast lineages in breast stroma
title_short Evidence of two distinct functionally specialized fibroblast lineages in breast stroma
title_sort evidence of two distinct functionally specialized fibroblast lineages in breast stroma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093959/
https://www.ncbi.nlm.nih.gov/pubmed/27809866
http://dx.doi.org/10.1186/s13058-016-0769-2
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