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Cell Proliferation, Movement and Differentiation during Maintenance of the Adult Mouse Adrenal Cortex
Appropriate maintenance and regeneration of adult endocrine organs is important in both normal physiology and disease. We investigated cell proliferation, movement and differentiation in the adult mouse adrenal cortex, using different 5-bromo-2'-deoxyuridine (BrdU) labelling regimens and immuno...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852665/ https://www.ncbi.nlm.nih.gov/pubmed/24324726 http://dx.doi.org/10.1371/journal.pone.0081865 |
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author | Chang, Su-Ping Morrison, Hamish D. Nilsson, Frida Kenyon, Christopher J. West, John D. Morley, Steven D. |
author_facet | Chang, Su-Ping Morrison, Hamish D. Nilsson, Frida Kenyon, Christopher J. West, John D. Morley, Steven D. |
author_sort | Chang, Su-Ping |
collection | PubMed |
description | Appropriate maintenance and regeneration of adult endocrine organs is important in both normal physiology and disease. We investigated cell proliferation, movement and differentiation in the adult mouse adrenal cortex, using different 5-bromo-2'-deoxyuridine (BrdU) labelling regimens and immunostaining for phenotypic steroidogenic cell markers. Pulse-labelling showed that cell division was largely confined to the outer cortex, with most cells moving inwards towards the medulla at around 13-20 µm per day, though a distinct labelled cell population remained in the outer 10% of the cortex. Pulse-chase-labelling coupled with phenotypic immunostaining showed that, unlike cells in the inner cortex, most BrdU-positive outer cortical cells did not express steroidogenic markers, while co-staining for BrdU and Ki67 revealed that some outer cortical BrdU-positive cells were induced to proliferate following acute adrenocorticotropic hormone (ACTH) treatment. Extended pulse-chase-labelling identified cells in the outer cortex which retained BrdU label for up to 18-23 weeks. Together, these observations are consistent with the location of both slow-cycling stem/progenitor and transiently amplifying cell populations in the outer cortex. Understanding the relationships between these distinct adrenocortical cell populations will be crucial to clarify mechanisms underpinning adrenocortical maintenance and long-term adaptation to pathophysiological states. |
format | Online Article Text |
id | pubmed-3852665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38526652013-12-09 Cell Proliferation, Movement and Differentiation during Maintenance of the Adult Mouse Adrenal Cortex Chang, Su-Ping Morrison, Hamish D. Nilsson, Frida Kenyon, Christopher J. West, John D. Morley, Steven D. PLoS One Research Article Appropriate maintenance and regeneration of adult endocrine organs is important in both normal physiology and disease. We investigated cell proliferation, movement and differentiation in the adult mouse adrenal cortex, using different 5-bromo-2'-deoxyuridine (BrdU) labelling regimens and immunostaining for phenotypic steroidogenic cell markers. Pulse-labelling showed that cell division was largely confined to the outer cortex, with most cells moving inwards towards the medulla at around 13-20 µm per day, though a distinct labelled cell population remained in the outer 10% of the cortex. Pulse-chase-labelling coupled with phenotypic immunostaining showed that, unlike cells in the inner cortex, most BrdU-positive outer cortical cells did not express steroidogenic markers, while co-staining for BrdU and Ki67 revealed that some outer cortical BrdU-positive cells were induced to proliferate following acute adrenocorticotropic hormone (ACTH) treatment. Extended pulse-chase-labelling identified cells in the outer cortex which retained BrdU label for up to 18-23 weeks. Together, these observations are consistent with the location of both slow-cycling stem/progenitor and transiently amplifying cell populations in the outer cortex. Understanding the relationships between these distinct adrenocortical cell populations will be crucial to clarify mechanisms underpinning adrenocortical maintenance and long-term adaptation to pathophysiological states. Public Library of Science 2013-12-04 /pmc/articles/PMC3852665/ /pubmed/24324726 http://dx.doi.org/10.1371/journal.pone.0081865 Text en © 2013 Chang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chang, Su-Ping Morrison, Hamish D. Nilsson, Frida Kenyon, Christopher J. West, John D. Morley, Steven D. Cell Proliferation, Movement and Differentiation during Maintenance of the Adult Mouse Adrenal Cortex |
title | Cell Proliferation, Movement and Differentiation during Maintenance of the Adult Mouse Adrenal Cortex |
title_full | Cell Proliferation, Movement and Differentiation during Maintenance of the Adult Mouse Adrenal Cortex |
title_fullStr | Cell Proliferation, Movement and Differentiation during Maintenance of the Adult Mouse Adrenal Cortex |
title_full_unstemmed | Cell Proliferation, Movement and Differentiation during Maintenance of the Adult Mouse Adrenal Cortex |
title_short | Cell Proliferation, Movement and Differentiation during Maintenance of the Adult Mouse Adrenal Cortex |
title_sort | cell proliferation, movement and differentiation during maintenance of the adult mouse adrenal cortex |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852665/ https://www.ncbi.nlm.nih.gov/pubmed/24324726 http://dx.doi.org/10.1371/journal.pone.0081865 |
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