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Aging differentially affects male and female neural stem cell neurogenic properties

PURPOSE: Neural stem cell transplantation as a brain repair strategy is a very promising technology. However, despite many attempts, the clinical success remains very deceiving. Despite clear evidence that sexual dimorphism rules many aspects of human biology, the occurrence of a sex difference in n...

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Detalles Bibliográficos
Autores principales: Waldron, Jay, McCourty, Althea, Lecanu, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781736/
https://www.ncbi.nlm.nih.gov/pubmed/24198517
http://dx.doi.org/10.2147/SCCAA.S13035
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author Waldron, Jay
McCourty, Althea
Lecanu, Laurent
author_facet Waldron, Jay
McCourty, Althea
Lecanu, Laurent
author_sort Waldron, Jay
collection PubMed
description PURPOSE: Neural stem cell transplantation as a brain repair strategy is a very promising technology. However, despite many attempts, the clinical success remains very deceiving. Despite clear evidence that sexual dimorphism rules many aspects of human biology, the occurrence of a sex difference in neural stem cell biology is largely understudied. Herein, we propose to determine whether gender is a dimension that drives the fate of neural stem cells through aging. Should it occur, we believe that neural stem cell sexual dimorphism and its variation during aging should be taken into account to refine clinical approaches of brain repair strategies. METHODS: Neural stem cells were isolated from the subventricular zone of three- and 20-month-old male and female Long-Evans rats. Expression of the estrogen receptors, ERα and ERβ, progesterone receptor, androgen receptor, and glucocorticoid receptor was analyzed and quantified by Western blotting on undifferentiated neural stem cells. A second set of neural stem cells was treated with retinoic acid to trigger differentiation, and the expression of neuronal, astroglial, and oligodendroglial markers was determined using Western blotting. CONCLUSION: We provided in vitro evidence that the fate of neural stem cells is affected by sex and aging. Indeed, young male neural stem cells mainly expressed markers of neuronal and oligodendroglial fate, whereas young female neural stem cells underwent differentiation towards an astroglial phenotype. Aging resulted in a lessened capacity to express neuron and astrocyte markers. Undifferentiated neural stem cells displayed sexual dimorphism in the expression of steroid receptors, in particular ERα and ERβ, and the expression level of several steroid receptors increased during aging. Such sexual dimorphism might explain, at least in part, the sex difference in neural fate we observed in young and old neural stem cells. These results suggest that sex and aging are two factors to be taken into consideration for future neural stem cell transplantation protocols in brain repair strategies.
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spelling pubmed-37817362013-11-06 Aging differentially affects male and female neural stem cell neurogenic properties Waldron, Jay McCourty, Althea Lecanu, Laurent Stem Cells Cloning Original Research PURPOSE: Neural stem cell transplantation as a brain repair strategy is a very promising technology. However, despite many attempts, the clinical success remains very deceiving. Despite clear evidence that sexual dimorphism rules many aspects of human biology, the occurrence of a sex difference in neural stem cell biology is largely understudied. Herein, we propose to determine whether gender is a dimension that drives the fate of neural stem cells through aging. Should it occur, we believe that neural stem cell sexual dimorphism and its variation during aging should be taken into account to refine clinical approaches of brain repair strategies. METHODS: Neural stem cells were isolated from the subventricular zone of three- and 20-month-old male and female Long-Evans rats. Expression of the estrogen receptors, ERα and ERβ, progesterone receptor, androgen receptor, and glucocorticoid receptor was analyzed and quantified by Western blotting on undifferentiated neural stem cells. A second set of neural stem cells was treated with retinoic acid to trigger differentiation, and the expression of neuronal, astroglial, and oligodendroglial markers was determined using Western blotting. CONCLUSION: We provided in vitro evidence that the fate of neural stem cells is affected by sex and aging. Indeed, young male neural stem cells mainly expressed markers of neuronal and oligodendroglial fate, whereas young female neural stem cells underwent differentiation towards an astroglial phenotype. Aging resulted in a lessened capacity to express neuron and astrocyte markers. Undifferentiated neural stem cells displayed sexual dimorphism in the expression of steroid receptors, in particular ERα and ERβ, and the expression level of several steroid receptors increased during aging. Such sexual dimorphism might explain, at least in part, the sex difference in neural fate we observed in young and old neural stem cells. These results suggest that sex and aging are two factors to be taken into consideration for future neural stem cell transplantation protocols in brain repair strategies. Dove Medical Press 2010-09-01 /pmc/articles/PMC3781736/ /pubmed/24198517 http://dx.doi.org/10.2147/SCCAA.S13035 Text en © 2010 Waldron et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Waldron, Jay
McCourty, Althea
Lecanu, Laurent
Aging differentially affects male and female neural stem cell neurogenic properties
title Aging differentially affects male and female neural stem cell neurogenic properties
title_full Aging differentially affects male and female neural stem cell neurogenic properties
title_fullStr Aging differentially affects male and female neural stem cell neurogenic properties
title_full_unstemmed Aging differentially affects male and female neural stem cell neurogenic properties
title_short Aging differentially affects male and female neural stem cell neurogenic properties
title_sort aging differentially affects male and female neural stem cell neurogenic properties
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781736/
https://www.ncbi.nlm.nih.gov/pubmed/24198517
http://dx.doi.org/10.2147/SCCAA.S13035
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