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Adipocyte hypertrophy and lipid dynamics underlie mammary gland remodeling after lactation
Adipocytes undergo pronounced changes in size and behavior to support diverse tissue functions, but the mechanisms that control these changes are not well understood. Mammary gland-associated white adipose tissue (mgWAT) regresses in support of milk fat production during lactation and expands during...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123393/ https://www.ncbi.nlm.nih.gov/pubmed/30181538 http://dx.doi.org/10.1038/s41467-018-05911-0 |
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author | Zwick, Rachel K. Rudolph, Michael C. Shook, Brett A. Holtrup, Brandon Roth, Eve Lei, Vivian Van Keymeulen, Alexandra Seewaldt, Victoria Kwei, Stephanie Wysolmerski, John Rodeheffer, Matthew S. Horsley, Valerie |
author_facet | Zwick, Rachel K. Rudolph, Michael C. Shook, Brett A. Holtrup, Brandon Roth, Eve Lei, Vivian Van Keymeulen, Alexandra Seewaldt, Victoria Kwei, Stephanie Wysolmerski, John Rodeheffer, Matthew S. Horsley, Valerie |
author_sort | Zwick, Rachel K. |
collection | PubMed |
description | Adipocytes undergo pronounced changes in size and behavior to support diverse tissue functions, but the mechanisms that control these changes are not well understood. Mammary gland-associated white adipose tissue (mgWAT) regresses in support of milk fat production during lactation and expands during the subsequent involution of milk-producing epithelial cells, providing one of the most marked physiological examples of adipose growth. We examined cellular mechanisms and functional implications of adipocyte and lipid dynamics in the mouse mammary gland (MG). Using in vivo analysis of adipocyte precursors and genetic tracing of mature adipocytes, we find mature adipocyte hypertrophy to be a primary mechanism of mgWAT expansion during involution. Lipid tracking and lipidomics demonstrate that adipocytes fill with epithelial-derived milk lipid. Furthermore, ablation of mgWAT during involution reveals an essential role for adipocytes in milk trafficking from, and proper restructuring of, the mammary epithelium. This work advances our understanding of MG remodeling and tissue-specific roles for adipocytes. |
format | Online Article Text |
id | pubmed-6123393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61233932018-09-06 Adipocyte hypertrophy and lipid dynamics underlie mammary gland remodeling after lactation Zwick, Rachel K. Rudolph, Michael C. Shook, Brett A. Holtrup, Brandon Roth, Eve Lei, Vivian Van Keymeulen, Alexandra Seewaldt, Victoria Kwei, Stephanie Wysolmerski, John Rodeheffer, Matthew S. Horsley, Valerie Nat Commun Article Adipocytes undergo pronounced changes in size and behavior to support diverse tissue functions, but the mechanisms that control these changes are not well understood. Mammary gland-associated white adipose tissue (mgWAT) regresses in support of milk fat production during lactation and expands during the subsequent involution of milk-producing epithelial cells, providing one of the most marked physiological examples of adipose growth. We examined cellular mechanisms and functional implications of adipocyte and lipid dynamics in the mouse mammary gland (MG). Using in vivo analysis of adipocyte precursors and genetic tracing of mature adipocytes, we find mature adipocyte hypertrophy to be a primary mechanism of mgWAT expansion during involution. Lipid tracking and lipidomics demonstrate that adipocytes fill with epithelial-derived milk lipid. Furthermore, ablation of mgWAT during involution reveals an essential role for adipocytes in milk trafficking from, and proper restructuring of, the mammary epithelium. This work advances our understanding of MG remodeling and tissue-specific roles for adipocytes. Nature Publishing Group UK 2018-09-04 /pmc/articles/PMC6123393/ /pubmed/30181538 http://dx.doi.org/10.1038/s41467-018-05911-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zwick, Rachel K. Rudolph, Michael C. Shook, Brett A. Holtrup, Brandon Roth, Eve Lei, Vivian Van Keymeulen, Alexandra Seewaldt, Victoria Kwei, Stephanie Wysolmerski, John Rodeheffer, Matthew S. Horsley, Valerie Adipocyte hypertrophy and lipid dynamics underlie mammary gland remodeling after lactation |
title | Adipocyte hypertrophy and lipid dynamics underlie mammary gland remodeling after lactation |
title_full | Adipocyte hypertrophy and lipid dynamics underlie mammary gland remodeling after lactation |
title_fullStr | Adipocyte hypertrophy and lipid dynamics underlie mammary gland remodeling after lactation |
title_full_unstemmed | Adipocyte hypertrophy and lipid dynamics underlie mammary gland remodeling after lactation |
title_short | Adipocyte hypertrophy and lipid dynamics underlie mammary gland remodeling after lactation |
title_sort | adipocyte hypertrophy and lipid dynamics underlie mammary gland remodeling after lactation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123393/ https://www.ncbi.nlm.nih.gov/pubmed/30181538 http://dx.doi.org/10.1038/s41467-018-05911-0 |
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