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The expression and localization of inhibin isotypes in mouse testis during postnatal development

Inhibin, which is important for normal gonadal function, acts on the pituitary gonadotropins to suppress follicle-stimulating hormone (FSH) secretion. The level and cellular localization of the inhibin isotypes, α, β(A) and β(B), in the testis of mice were examined during postnatal development in or...

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Autores principales: Kim, Yujin, Kim, Joong-Sun, Song, Myoung-Sub, Seo, Heung-Sik, Kim, Jong Choon, Bae, Chun-Sik, Kim, Seungjoon, Shin, Taekyun, Kim, Sung-Ho, Moon, Changjong
Formato: Texto
Lenguaje:English
Publicado: The Korean Society of Veterinary Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811774/
https://www.ncbi.nlm.nih.gov/pubmed/19043308
http://dx.doi.org/10.4142/jvs.2008.9.4.345
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author Kim, Yujin
Kim, Joong-Sun
Song, Myoung-Sub
Seo, Heung-Sik
Kim, Jong Choon
Bae, Chun-Sik
Kim, Seungjoon
Shin, Taekyun
Kim, Sung-Ho
Moon, Changjong
author_facet Kim, Yujin
Kim, Joong-Sun
Song, Myoung-Sub
Seo, Heung-Sik
Kim, Jong Choon
Bae, Chun-Sik
Kim, Seungjoon
Shin, Taekyun
Kim, Sung-Ho
Moon, Changjong
author_sort Kim, Yujin
collection PubMed
description Inhibin, which is important for normal gonadal function, acts on the pituitary gonadotropins to suppress follicle-stimulating hormone (FSH) secretion. The level and cellular localization of the inhibin isotypes, α, β(A) and β(B), in the testis of mice were examined during postnatal development in order to determine if inhibin expression is related to testicular maturation. Mouse testes were sampled on postnatal days (PNDs) 1, 3, 6, 18, 48 and 120, and analyzed by Western blotting and immunofluorescence. Western blot analysis showed very low levels of inhibin α, β(A) and β(B) expression in the testes at days 1 to 6 after birth. The levels then increased gradually from PND 18 to 48-120, and there were significant peaks at PND 48. Inhibin α, β(A) and β(B) were detected in testicular cells during postnatal development using immunohistochemistry. The immunoreactivity of inhibin α was rarely observed in testicular cells during PND 1 to 6, or in the cytoplasmic process of Sertoli cells surrounding the germ cells and interstitial cells during PND 18 to 120. Inhibin β(A) and β(B) immunoreactivity was rarely observed in the testis from PND 1 to 6. On the other hand, it was observed in some spermatogonial cells, as well as in the interstitial space between PND 48 and PND 120. We conclude that the expression of inhibin isotypes increases progressively in the testis of mice with increasing postnatal age, suggesting that inhibin is associated with a negative feedback signal for FSH in testicular maturation.
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spelling pubmed-28117742010-01-28 The expression and localization of inhibin isotypes in mouse testis during postnatal development Kim, Yujin Kim, Joong-Sun Song, Myoung-Sub Seo, Heung-Sik Kim, Jong Choon Bae, Chun-Sik Kim, Seungjoon Shin, Taekyun Kim, Sung-Ho Moon, Changjong J Vet Sci Original Article Inhibin, which is important for normal gonadal function, acts on the pituitary gonadotropins to suppress follicle-stimulating hormone (FSH) secretion. The level and cellular localization of the inhibin isotypes, α, β(A) and β(B), in the testis of mice were examined during postnatal development in order to determine if inhibin expression is related to testicular maturation. Mouse testes were sampled on postnatal days (PNDs) 1, 3, 6, 18, 48 and 120, and analyzed by Western blotting and immunofluorescence. Western blot analysis showed very low levels of inhibin α, β(A) and β(B) expression in the testes at days 1 to 6 after birth. The levels then increased gradually from PND 18 to 48-120, and there were significant peaks at PND 48. Inhibin α, β(A) and β(B) were detected in testicular cells during postnatal development using immunohistochemistry. The immunoreactivity of inhibin α was rarely observed in testicular cells during PND 1 to 6, or in the cytoplasmic process of Sertoli cells surrounding the germ cells and interstitial cells during PND 18 to 120. Inhibin β(A) and β(B) immunoreactivity was rarely observed in the testis from PND 1 to 6. On the other hand, it was observed in some spermatogonial cells, as well as in the interstitial space between PND 48 and PND 120. We conclude that the expression of inhibin isotypes increases progressively in the testis of mice with increasing postnatal age, suggesting that inhibin is associated with a negative feedback signal for FSH in testicular maturation. The Korean Society of Veterinary Science 2008-12 2008-12-31 /pmc/articles/PMC2811774/ /pubmed/19043308 http://dx.doi.org/10.4142/jvs.2008.9.4.345 Text en Copyright © 2008 The Korean Society of Veterinary Science https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Yujin
Kim, Joong-Sun
Song, Myoung-Sub
Seo, Heung-Sik
Kim, Jong Choon
Bae, Chun-Sik
Kim, Seungjoon
Shin, Taekyun
Kim, Sung-Ho
Moon, Changjong
The expression and localization of inhibin isotypes in mouse testis during postnatal development
title The expression and localization of inhibin isotypes in mouse testis during postnatal development
title_full The expression and localization of inhibin isotypes in mouse testis during postnatal development
title_fullStr The expression and localization of inhibin isotypes in mouse testis during postnatal development
title_full_unstemmed The expression and localization of inhibin isotypes in mouse testis during postnatal development
title_short The expression and localization of inhibin isotypes in mouse testis during postnatal development
title_sort expression and localization of inhibin isotypes in mouse testis during postnatal development
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811774/
https://www.ncbi.nlm.nih.gov/pubmed/19043308
http://dx.doi.org/10.4142/jvs.2008.9.4.345
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