Role of neural stem cell activity in postweaning development of the sexually dimorphic nucleus of the preoptic area in rats.

The sexually dimorphic nucleus of the preoptic area (SDN-POA) has received increased attention due to its apparent sensitivity to estrogen-like compounds found in food and food containers. The mechanisms that regulate SDN-POA volume remain unclear as is the extent of postweaning development of the S...

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Main Authors: Zhen He, Sherry A Ferguson, Li Cui, L John Greenfield, Merle G Paule
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3559780?pdf=render
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spelling doaj-e796eb574ac04f25827843fe1513234d2020-11-24T20:49:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5492710.1371/journal.pone.0054927Role of neural stem cell activity in postweaning development of the sexually dimorphic nucleus of the preoptic area in rats.Zhen HeSherry A FergusonLi CuiL John GreenfieldMerle G PauleThe sexually dimorphic nucleus of the preoptic area (SDN-POA) has received increased attention due to its apparent sensitivity to estrogen-like compounds found in food and food containers. The mechanisms that regulate SDN-POA volume remain unclear as is the extent of postweaning development of the SDN-POA. Here we demonstrate that the female Sprague-Dawley SDN-POA volume increased from weaning to adulthood, although this increase was not statistically significant as it was in males. The number of cells positive for Ki67, a marker of cell proliferation, in both the SDN-POA and the hypothalamus was significantly higher at weaning than at adulthood in male rats. In contrast, the number of Ki67-positive cells was significantly higher in the hypothalamus but not in the SDN-POA (p>0.05) at weaning than at adulthood in female rats. A subset of the Ki67-positive cells in the SDN-POA displayed the morphology of dividing cells. Nestin-immunoreactivity delineated a potential macroscopic neural stem cell niche in the rostral end of the 3rd ventricle. In conclusion, stem cells may partially account for the sexually dimorphic postweaning development of the SDN-POA.http://europepmc.org/articles/PMC3559780?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Zhen He
Sherry A Ferguson
Li Cui
L John Greenfield
Merle G Paule
spellingShingle Zhen He
Sherry A Ferguson
Li Cui
L John Greenfield
Merle G Paule
Role of neural stem cell activity in postweaning development of the sexually dimorphic nucleus of the preoptic area in rats.
PLoS ONE
author_facet Zhen He
Sherry A Ferguson
Li Cui
L John Greenfield
Merle G Paule
author_sort Zhen He
title Role of neural stem cell activity in postweaning development of the sexually dimorphic nucleus of the preoptic area in rats.
title_short Role of neural stem cell activity in postweaning development of the sexually dimorphic nucleus of the preoptic area in rats.
title_full Role of neural stem cell activity in postweaning development of the sexually dimorphic nucleus of the preoptic area in rats.
title_fullStr Role of neural stem cell activity in postweaning development of the sexually dimorphic nucleus of the preoptic area in rats.
title_full_unstemmed Role of neural stem cell activity in postweaning development of the sexually dimorphic nucleus of the preoptic area in rats.
title_sort role of neural stem cell activity in postweaning development of the sexually dimorphic nucleus of the preoptic area in rats.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description The sexually dimorphic nucleus of the preoptic area (SDN-POA) has received increased attention due to its apparent sensitivity to estrogen-like compounds found in food and food containers. The mechanisms that regulate SDN-POA volume remain unclear as is the extent of postweaning development of the SDN-POA. Here we demonstrate that the female Sprague-Dawley SDN-POA volume increased from weaning to adulthood, although this increase was not statistically significant as it was in males. The number of cells positive for Ki67, a marker of cell proliferation, in both the SDN-POA and the hypothalamus was significantly higher at weaning than at adulthood in male rats. In contrast, the number of Ki67-positive cells was significantly higher in the hypothalamus but not in the SDN-POA (p>0.05) at weaning than at adulthood in female rats. A subset of the Ki67-positive cells in the SDN-POA displayed the morphology of dividing cells. Nestin-immunoreactivity delineated a potential macroscopic neural stem cell niche in the rostral end of the 3rd ventricle. In conclusion, stem cells may partially account for the sexually dimorphic postweaning development of the SDN-POA.
url http://europepmc.org/articles/PMC3559780?pdf=render
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