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A Mammary Organoid Model to Study Branching Morphogenesis
Branching morphogenesis is the process that gives rise to branched structures in several organs, such as the lung, the kidney, and the mammary gland. Although morphologically well described, the exact mechanisms driving branch elongation and bifurcation are still poorly understood. Signaling cues fr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988230/ https://www.ncbi.nlm.nih.gov/pubmed/35399282 http://dx.doi.org/10.3389/fphys.2022.826107 |
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author | Caruso, Marika Huang, Sjanie Mourao, Larissa Scheele, Colinda L. G. J. |
author_facet | Caruso, Marika Huang, Sjanie Mourao, Larissa Scheele, Colinda L. G. J. |
author_sort | Caruso, Marika |
collection | PubMed |
description | Branching morphogenesis is the process that gives rise to branched structures in several organs, such as the lung, the kidney, and the mammary gland. Although morphologically well described, the exact mechanisms driving branch elongation and bifurcation are still poorly understood. Signaling cues from the stroma and extracellular matrix have an important role in driving branching morphogenesis. Organoid models derived from primary mammary epithelial cells have emerged as a powerful tool to gain insight into branching morphogenesis of the mammary gland. However, current available mammary organoid culture protocols result in morphologically simple structures which do not resemble the complex branched structure of the in vivo mammary gland. Supplementation of growth factors to mammary organoids cultured in basement membrane extract or collagen I were shown to induce bud formation and elongation but are not sufficient to drive true branching events. Here, we present an improved culture approach based on 3D primary mammary epithelial cell culture to develop branched organoids with a complex morphology. By alternating the addition of fibroblast growth factor 2 and epidermal growth factor to mammary organoids cultured in a basement membrane extract matrix enriched with collagen type I fibers, we obtain complex mammary organoid structures with primary, secondary, and tertiary branches over a period of 15–20 days. Mammary organoid structures grow >1 mm in size and show an elongated and branched shape which resembles in vivo mammary gland morphology. This novel branched mammary organoid model offers many possibilities to study the mechanisms of branching in the developing mammary gland. |
format | Online Article Text |
id | pubmed-8988230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89882302022-04-08 A Mammary Organoid Model to Study Branching Morphogenesis Caruso, Marika Huang, Sjanie Mourao, Larissa Scheele, Colinda L. G. J. Front Physiol Physiology Branching morphogenesis is the process that gives rise to branched structures in several organs, such as the lung, the kidney, and the mammary gland. Although morphologically well described, the exact mechanisms driving branch elongation and bifurcation are still poorly understood. Signaling cues from the stroma and extracellular matrix have an important role in driving branching morphogenesis. Organoid models derived from primary mammary epithelial cells have emerged as a powerful tool to gain insight into branching morphogenesis of the mammary gland. However, current available mammary organoid culture protocols result in morphologically simple structures which do not resemble the complex branched structure of the in vivo mammary gland. Supplementation of growth factors to mammary organoids cultured in basement membrane extract or collagen I were shown to induce bud formation and elongation but are not sufficient to drive true branching events. Here, we present an improved culture approach based on 3D primary mammary epithelial cell culture to develop branched organoids with a complex morphology. By alternating the addition of fibroblast growth factor 2 and epidermal growth factor to mammary organoids cultured in a basement membrane extract matrix enriched with collagen type I fibers, we obtain complex mammary organoid structures with primary, secondary, and tertiary branches over a period of 15–20 days. Mammary organoid structures grow >1 mm in size and show an elongated and branched shape which resembles in vivo mammary gland morphology. This novel branched mammary organoid model offers many possibilities to study the mechanisms of branching in the developing mammary gland. Frontiers Media S.A. 2022-03-16 /pmc/articles/PMC8988230/ /pubmed/35399282 http://dx.doi.org/10.3389/fphys.2022.826107 Text en Copyright © 2022 Caruso, Huang, Mourao and Scheele. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Caruso, Marika Huang, Sjanie Mourao, Larissa Scheele, Colinda L. G. J. A Mammary Organoid Model to Study Branching Morphogenesis |
title | A Mammary Organoid Model to Study Branching Morphogenesis |
title_full | A Mammary Organoid Model to Study Branching Morphogenesis |
title_fullStr | A Mammary Organoid Model to Study Branching Morphogenesis |
title_full_unstemmed | A Mammary Organoid Model to Study Branching Morphogenesis |
title_short | A Mammary Organoid Model to Study Branching Morphogenesis |
title_sort | mammary organoid model to study branching morphogenesis |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988230/ https://www.ncbi.nlm.nih.gov/pubmed/35399282 http://dx.doi.org/10.3389/fphys.2022.826107 |
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