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INSL3 stimulates spermatogonial differentiation in testis of adult zebrafish (Danio rerio)

INSL3 (insulin-like peptide 3) is a relaxin peptide family member expressed by Leydig cells in the vertebrate testis. In mammals, INSL3 mediates testicular descent during embryogenesis but information on its function in adults is limited. In fish, the testes remain in the body cavity, although the i...

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Autores principales: Assis, L. H. C., Crespo, D., Morais, R. D. V. S., França, L. R., Bogerd, J., Schulz, R. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735252/
https://www.ncbi.nlm.nih.gov/pubmed/26077926
http://dx.doi.org/10.1007/s00441-015-2213-9
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author Assis, L. H. C.
Crespo, D.
Morais, R. D. V. S.
França, L. R.
Bogerd, J.
Schulz, R. W.
author_facet Assis, L. H. C.
Crespo, D.
Morais, R. D. V. S.
França, L. R.
Bogerd, J.
Schulz, R. W.
author_sort Assis, L. H. C.
collection PubMed
description INSL3 (insulin-like peptide 3) is a relaxin peptide family member expressed by Leydig cells in the vertebrate testis. In mammals, INSL3 mediates testicular descent during embryogenesis but information on its function in adults is limited. In fish, the testes remain in the body cavity, although the insl3 gene is still expressed, suggesting yet undiscovered, evolutionary older functions. Anti-Müllerian hormone (Amh), in addition to inhibiting spermatogonial differentiation and androgen release, inhibits the Fsh (follicle-stimulating hormone)-induced increase in insl3 transcript levels in zebrafish testis. Therefore, the two growth factors might have antagonistic effects. We examine human INSL3 (hINSL3) effects on zebrafish germ cell proliferation/differentiation and androgen release by using a testis tissue culture system. hINSL3 increases the proliferation of type A undifferentiated (A(und)) but not of type A differentiating (A(diff)) spermatogonia, while reducing the proliferation of Sertoli cells associated with proliferating A(und). Since the area occupied by A(und) decreases and that of A(diff) increases, we conclude that hINSL3 recruits A(und) into differentiation; this is supported by the hINSL3-induced down-regulation of nanos2 transcript levels, a marker of single A(und) spermatogonia in zebrafish and other vertebrates. Pulse-chase experiments with a mitosis marker also indicate that hINSL3 promotes spermatogonial differentiation. However, hINSL3 does not modulate basal or Fsh-stimulated androgen release or growth factor transcript levels, including those of amh. Thus, hINSL3 seems to recruit A(und) spermatogonia into differentiation, potentially mediating an Fsh effect on spermatogenesis.
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spelling pubmed-47352522016-02-09 INSL3 stimulates spermatogonial differentiation in testis of adult zebrafish (Danio rerio) Assis, L. H. C. Crespo, D. Morais, R. D. V. S. França, L. R. Bogerd, J. Schulz, R. W. Cell Tissue Res Regular Article INSL3 (insulin-like peptide 3) is a relaxin peptide family member expressed by Leydig cells in the vertebrate testis. In mammals, INSL3 mediates testicular descent during embryogenesis but information on its function in adults is limited. In fish, the testes remain in the body cavity, although the insl3 gene is still expressed, suggesting yet undiscovered, evolutionary older functions. Anti-Müllerian hormone (Amh), in addition to inhibiting spermatogonial differentiation and androgen release, inhibits the Fsh (follicle-stimulating hormone)-induced increase in insl3 transcript levels in zebrafish testis. Therefore, the two growth factors might have antagonistic effects. We examine human INSL3 (hINSL3) effects on zebrafish germ cell proliferation/differentiation and androgen release by using a testis tissue culture system. hINSL3 increases the proliferation of type A undifferentiated (A(und)) but not of type A differentiating (A(diff)) spermatogonia, while reducing the proliferation of Sertoli cells associated with proliferating A(und). Since the area occupied by A(und) decreases and that of A(diff) increases, we conclude that hINSL3 recruits A(und) into differentiation; this is supported by the hINSL3-induced down-regulation of nanos2 transcript levels, a marker of single A(und) spermatogonia in zebrafish and other vertebrates. Pulse-chase experiments with a mitosis marker also indicate that hINSL3 promotes spermatogonial differentiation. However, hINSL3 does not modulate basal or Fsh-stimulated androgen release or growth factor transcript levels, including those of amh. Thus, hINSL3 seems to recruit A(und) spermatogonia into differentiation, potentially mediating an Fsh effect on spermatogenesis. Springer Berlin Heidelberg 2015-06-16 2016 /pmc/articles/PMC4735252/ /pubmed/26077926 http://dx.doi.org/10.1007/s00441-015-2213-9 Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made.
spellingShingle Regular Article
Assis, L. H. C.
Crespo, D.
Morais, R. D. V. S.
França, L. R.
Bogerd, J.
Schulz, R. W.
INSL3 stimulates spermatogonial differentiation in testis of adult zebrafish (Danio rerio)
title INSL3 stimulates spermatogonial differentiation in testis of adult zebrafish (Danio rerio)
title_full INSL3 stimulates spermatogonial differentiation in testis of adult zebrafish (Danio rerio)
title_fullStr INSL3 stimulates spermatogonial differentiation in testis of adult zebrafish (Danio rerio)
title_full_unstemmed INSL3 stimulates spermatogonial differentiation in testis of adult zebrafish (Danio rerio)
title_short INSL3 stimulates spermatogonial differentiation in testis of adult zebrafish (Danio rerio)
title_sort insl3 stimulates spermatogonial differentiation in testis of adult zebrafish (danio rerio)
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735252/
https://www.ncbi.nlm.nih.gov/pubmed/26077926
http://dx.doi.org/10.1007/s00441-015-2213-9
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