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Induction of spermatogenic synchrony by retinoic acid in neonatal mice

Retinoic acid (RA) is required for the successful differentiation and meiotic entry of germ cells in the murine testis. The availability of RA to undifferentiated germ cells begins in a variable, uneven pattern during the first few days after birth and establishes the asynchronous pattern of germ ce...

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Autores principales: Davis, Jeffrey C., Snyder, Elizabeth M., Hogarth, Cathryn A., Small, Christopher, Griswold, Michael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644044/
https://www.ncbi.nlm.nih.gov/pubmed/23687613
http://dx.doi.org/10.4161/spmg.23180
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author Davis, Jeffrey C.
Snyder, Elizabeth M.
Hogarth, Cathryn A.
Small, Christopher
Griswold, Michael D.
author_facet Davis, Jeffrey C.
Snyder, Elizabeth M.
Hogarth, Cathryn A.
Small, Christopher
Griswold, Michael D.
author_sort Davis, Jeffrey C.
collection PubMed
description Retinoic acid (RA) is required for the successful differentiation and meiotic entry of germ cells in the murine testis. The availability of RA to undifferentiated germ cells begins in a variable, uneven pattern during the first few days after birth and establishes the asynchronous pattern of germ cell differentiation in adulthood. It has been shown that synchronous spermatogenesis can be induced in 2 d postpartum mice, but not in adult mice, by treating vitamin A sufficient males with RA. In this study, neonatal males were treated at different ages with a single dose of RA and spermatogenesis was examined after recovery to adulthood. The failure of exogenous RA to alter asynchrony correlates with the appearance of meiotic preleptotene spermatocytes within the seminiferous epithelium.
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spelling pubmed-36440442013-05-17 Induction of spermatogenic synchrony by retinoic acid in neonatal mice Davis, Jeffrey C. Snyder, Elizabeth M. Hogarth, Cathryn A. Small, Christopher Griswold, Michael D. Spermatogenesis Letter to the Editor Retinoic acid (RA) is required for the successful differentiation and meiotic entry of germ cells in the murine testis. The availability of RA to undifferentiated germ cells begins in a variable, uneven pattern during the first few days after birth and establishes the asynchronous pattern of germ cell differentiation in adulthood. It has been shown that synchronous spermatogenesis can be induced in 2 d postpartum mice, but not in adult mice, by treating vitamin A sufficient males with RA. In this study, neonatal males were treated at different ages with a single dose of RA and spermatogenesis was examined after recovery to adulthood. The failure of exogenous RA to alter asynchrony correlates with the appearance of meiotic preleptotene spermatocytes within the seminiferous epithelium. Landes Bioscience 2013-01-01 /pmc/articles/PMC3644044/ /pubmed/23687613 http://dx.doi.org/10.4161/spmg.23180 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Letter to the Editor
Davis, Jeffrey C.
Snyder, Elizabeth M.
Hogarth, Cathryn A.
Small, Christopher
Griswold, Michael D.
Induction of spermatogenic synchrony by retinoic acid in neonatal mice
title Induction of spermatogenic synchrony by retinoic acid in neonatal mice
title_full Induction of spermatogenic synchrony by retinoic acid in neonatal mice
title_fullStr Induction of spermatogenic synchrony by retinoic acid in neonatal mice
title_full_unstemmed Induction of spermatogenic synchrony by retinoic acid in neonatal mice
title_short Induction of spermatogenic synchrony by retinoic acid in neonatal mice
title_sort induction of spermatogenic synchrony by retinoic acid in neonatal mice
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644044/
https://www.ncbi.nlm.nih.gov/pubmed/23687613
http://dx.doi.org/10.4161/spmg.23180
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