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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...

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Autores principales: Chang, Su-Ping, Morrison, Hamish D., Nilsson, Frida, Kenyon, Christopher J., West, John D., Morley, Steven D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
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.
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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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