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Mammary extracellular matrix directs differentiation of testicular and embryonic stem cells to form functional mammary glands in vivo

Previously, we demonstrated the ability of the normal mammary microenvironment (niche) to direct non-mammary cells including testicular and embryonic stem cells (ESCs) to adopt a mammary epithelial cell (MEC) fate. These studies relied upon the interaction of transplanted normal MECs with non-mammar...

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Autores principales: Bruno, Robert D., Fleming, Jodie M., George, Andrea L., Boulanger, Corinne A., Schedin, Pepper, Smith, Gilbert H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223207/
https://www.ncbi.nlm.nih.gov/pubmed/28071703
http://dx.doi.org/10.1038/srep40196
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author Bruno, Robert D.
Fleming, Jodie M.
George, Andrea L.
Boulanger, Corinne A.
Schedin, Pepper
Smith, Gilbert H.
author_facet Bruno, Robert D.
Fleming, Jodie M.
George, Andrea L.
Boulanger, Corinne A.
Schedin, Pepper
Smith, Gilbert H.
author_sort Bruno, Robert D.
collection PubMed
description Previously, we demonstrated the ability of the normal mammary microenvironment (niche) to direct non-mammary cells including testicular and embryonic stem cells (ESCs) to adopt a mammary epithelial cell (MEC) fate. These studies relied upon the interaction of transplanted normal MECs with non-mammary cells within the mammary fat-pads of recipient mice that had their endogenous epithelium removed. Here, we tested whether acellular mammary extracellular matrix (mECM) preparations are sufficient to direct differentiation of testicular-derived cells and ESCs to form functional mammary epithelial trees in vivo. We found that mECMs isolated from adult mice and rats were sufficient to redirect testicular derived cells to produce normal mammary epithelial trees within epithelial divested mouse mammary fat-pads. Conversely, ECMs isolated from omental fat and lung did not redirect testicular cells to a MEC fate, indicating the necessity of tissue specific components of the mECM. mECM preparations also completely inhibited teratoma formation from ESC inoculations. Further, a phenotypically normal ductal outgrowth resulted from a single inoculation of ESCs and mECM. To the best of our knowledge, this is the first demonstration of a tissue specific ECM driving differentiation of cells to form a functional tissue in vivo.
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spelling pubmed-52232072017-01-17 Mammary extracellular matrix directs differentiation of testicular and embryonic stem cells to form functional mammary glands in vivo Bruno, Robert D. Fleming, Jodie M. George, Andrea L. Boulanger, Corinne A. Schedin, Pepper Smith, Gilbert H. Sci Rep Article Previously, we demonstrated the ability of the normal mammary microenvironment (niche) to direct non-mammary cells including testicular and embryonic stem cells (ESCs) to adopt a mammary epithelial cell (MEC) fate. These studies relied upon the interaction of transplanted normal MECs with non-mammary cells within the mammary fat-pads of recipient mice that had their endogenous epithelium removed. Here, we tested whether acellular mammary extracellular matrix (mECM) preparations are sufficient to direct differentiation of testicular-derived cells and ESCs to form functional mammary epithelial trees in vivo. We found that mECMs isolated from adult mice and rats were sufficient to redirect testicular derived cells to produce normal mammary epithelial trees within epithelial divested mouse mammary fat-pads. Conversely, ECMs isolated from omental fat and lung did not redirect testicular cells to a MEC fate, indicating the necessity of tissue specific components of the mECM. mECM preparations also completely inhibited teratoma formation from ESC inoculations. Further, a phenotypically normal ductal outgrowth resulted from a single inoculation of ESCs and mECM. To the best of our knowledge, this is the first demonstration of a tissue specific ECM driving differentiation of cells to form a functional tissue in vivo. Nature Publishing Group 2017-01-10 /pmc/articles/PMC5223207/ /pubmed/28071703 http://dx.doi.org/10.1038/srep40196 Text en Copyright © 2017, 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
Bruno, Robert D.
Fleming, Jodie M.
George, Andrea L.
Boulanger, Corinne A.
Schedin, Pepper
Smith, Gilbert H.
Mammary extracellular matrix directs differentiation of testicular and embryonic stem cells to form functional mammary glands in vivo
title Mammary extracellular matrix directs differentiation of testicular and embryonic stem cells to form functional mammary glands in vivo
title_full Mammary extracellular matrix directs differentiation of testicular and embryonic stem cells to form functional mammary glands in vivo
title_fullStr Mammary extracellular matrix directs differentiation of testicular and embryonic stem cells to form functional mammary glands in vivo
title_full_unstemmed Mammary extracellular matrix directs differentiation of testicular and embryonic stem cells to form functional mammary glands in vivo
title_short Mammary extracellular matrix directs differentiation of testicular and embryonic stem cells to form functional mammary glands in vivo
title_sort mammary extracellular matrix directs differentiation of testicular and embryonic stem cells to form functional mammary glands in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223207/
https://www.ncbi.nlm.nih.gov/pubmed/28071703
http://dx.doi.org/10.1038/srep40196
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