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Developing ovine mammary terminal duct lobular units have a dynamic mucosal and stromal immune microenvironment
The human breast and ovine mammary gland undergo striking levels of postnatal development, leading to formation of terminal duct lobular units (TDLUs). Here we interrogate aspects of sheep TDLU growth as a model of breast development and to increase understanding of ovine mammogenesis. The distribut...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379191/ https://www.ncbi.nlm.nih.gov/pubmed/34417554 http://dx.doi.org/10.1038/s42003-021-02502-6 |
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author | Nagy, Dorottya Gillis, Clare M. C. Davies, Katie Fowden, Abigail L. Rees, Paul Wills, John W. Hughes, Katherine |
author_facet | Nagy, Dorottya Gillis, Clare M. C. Davies, Katie Fowden, Abigail L. Rees, Paul Wills, John W. Hughes, Katherine |
author_sort | Nagy, Dorottya |
collection | PubMed |
description | The human breast and ovine mammary gland undergo striking levels of postnatal development, leading to formation of terminal duct lobular units (TDLUs). Here we interrogate aspects of sheep TDLU growth as a model of breast development and to increase understanding of ovine mammogenesis. The distributions of epithelial nuclear Ki67 positivity differ significantly between younger and older lambs. Ki67 expression is polarised to the leading edge of the developing TDLUs. Intraepithelial ductal macrophages exhibit periodicity and considerably increased density in lambs approaching puberty. Stromal macrophages are more abundant centrally than peripherally. Intraepithelial T lymphocytes are more numerous in older lambs. Stromal hotspots of Ki67 expression colocalize with immune cell aggregates that exhibit distinct organisation consistent with tertiary lymphoid structures. The lamb mammary gland thus exhibits a dynamic mucosal and stromal immune microenvironment and constitutes a valuable model system that provides new insights into postnatal breast development. |
format | Online Article Text |
id | pubmed-8379191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83791912021-09-22 Developing ovine mammary terminal duct lobular units have a dynamic mucosal and stromal immune microenvironment Nagy, Dorottya Gillis, Clare M. C. Davies, Katie Fowden, Abigail L. Rees, Paul Wills, John W. Hughes, Katherine Commun Biol Article The human breast and ovine mammary gland undergo striking levels of postnatal development, leading to formation of terminal duct lobular units (TDLUs). Here we interrogate aspects of sheep TDLU growth as a model of breast development and to increase understanding of ovine mammogenesis. The distributions of epithelial nuclear Ki67 positivity differ significantly between younger and older lambs. Ki67 expression is polarised to the leading edge of the developing TDLUs. Intraepithelial ductal macrophages exhibit periodicity and considerably increased density in lambs approaching puberty. Stromal macrophages are more abundant centrally than peripherally. Intraepithelial T lymphocytes are more numerous in older lambs. Stromal hotspots of Ki67 expression colocalize with immune cell aggregates that exhibit distinct organisation consistent with tertiary lymphoid structures. The lamb mammary gland thus exhibits a dynamic mucosal and stromal immune microenvironment and constitutes a valuable model system that provides new insights into postnatal breast development. Nature Publishing Group UK 2021-08-20 /pmc/articles/PMC8379191/ /pubmed/34417554 http://dx.doi.org/10.1038/s42003-021-02502-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Nagy, Dorottya Gillis, Clare M. C. Davies, Katie Fowden, Abigail L. Rees, Paul Wills, John W. Hughes, Katherine Developing ovine mammary terminal duct lobular units have a dynamic mucosal and stromal immune microenvironment |
title | Developing ovine mammary terminal duct lobular units have a dynamic mucosal and stromal immune microenvironment |
title_full | Developing ovine mammary terminal duct lobular units have a dynamic mucosal and stromal immune microenvironment |
title_fullStr | Developing ovine mammary terminal duct lobular units have a dynamic mucosal and stromal immune microenvironment |
title_full_unstemmed | Developing ovine mammary terminal duct lobular units have a dynamic mucosal and stromal immune microenvironment |
title_short | Developing ovine mammary terminal duct lobular units have a dynamic mucosal and stromal immune microenvironment |
title_sort | developing ovine mammary terminal duct lobular units have a dynamic mucosal and stromal immune microenvironment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379191/ https://www.ncbi.nlm.nih.gov/pubmed/34417554 http://dx.doi.org/10.1038/s42003-021-02502-6 |
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