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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Main Authors: Su-Ping Chang, Hamish D Morrison, Frida Nilsson, Christopher J Kenyon, John D West, Steven D Morley
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3852665?pdf=render
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author Su-Ping Chang
Hamish D Morrison
Frida Nilsson
Christopher J Kenyon
John D West
Steven D Morley
author_facet Su-Ping Chang
Hamish D Morrison
Frida Nilsson
Christopher J Kenyon
John D West
Steven D Morley
author_sort Su-Ping Chang
collection DOAJ
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 doaj.art-a2b281f35c054c4b9d9f5d07019e4e9e2022-12-21T22:46:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01812e8186510.1371/journal.pone.0081865Cell proliferation, movement and differentiation during maintenance of the adult mouse adrenal cortex.Su-Ping ChangHamish D MorrisonFrida NilssonChristopher J KenyonJohn D WestSteven D MorleyAppropriate 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.http://europepmc.org/articles/PMC3852665?pdf=render
spellingShingle Su-Ping Chang
Hamish D Morrison
Frida Nilsson
Christopher J Kenyon
John D West
Steven D Morley
Cell proliferation, movement and differentiation during maintenance of the adult mouse adrenal cortex.
PLoS ONE
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
url http://europepmc.org/articles/PMC3852665?pdf=render
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