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Insulin-like 3 affects zebrafish spermatogenic cells directly and via Sertoli cells
Pituitary hormones can use local signaling molecules to regulate target tissue functions. In adult zebrafish testes, follicle-stimulating hormone (Fsh) strongly increases the production of insulin-like 3 (Insl3), a Leydig cell-derived growth factor found in all vertebrates. Little information is ava...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884674/ https://www.ncbi.nlm.nih.gov/pubmed/33589679 http://dx.doi.org/10.1038/s42003-021-01708-y |
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author | Crespo, Diego Assis, Luiz H. C. Zhang, Yu Ting Safian, Diego Furmanek, Tomasz Skaftnesmo, Kai Ove Norberg, Birgitta Ge, Wei Choi, Yung-Ching den Broeder, Marjo J. Legler, Juliette Bogerd, Jan Schulz, Rüdiger W. |
author_facet | Crespo, Diego Assis, Luiz H. C. Zhang, Yu Ting Safian, Diego Furmanek, Tomasz Skaftnesmo, Kai Ove Norberg, Birgitta Ge, Wei Choi, Yung-Ching den Broeder, Marjo J. Legler, Juliette Bogerd, Jan Schulz, Rüdiger W. |
author_sort | Crespo, Diego |
collection | PubMed |
description | Pituitary hormones can use local signaling molecules to regulate target tissue functions. In adult zebrafish testes, follicle-stimulating hormone (Fsh) strongly increases the production of insulin-like 3 (Insl3), a Leydig cell-derived growth factor found in all vertebrates. Little information is available regarding Insl3 function in adult spermatogenesis. The Insl3 receptors Rxfp2a and 2b were expressed by type A spermatogonia and Sertoli and myoid cells, respectively, in zebrafish testis tissue. Loss of insl3 increased germ cell apoptosis in males starting at 9 months of age, but spermatogenesis appeared normal in fully fertile, younger adults. Insl3 changed the expression of 409 testicular genes. Among others, retinoic acid (RA) signaling was up- and peroxisome proliferator-activated receptor gamma (Pparg) signaling was down-regulated. Follow-up studies showed that RA and Pparg signaling mediated Insl3 effects, resulting in the increased production of differentiating spermatogonia. This suggests that Insl3 recruits two locally active nuclear receptor pathways to implement pituitary (Fsh) stimulation of spermatogenesis. |
format | Online Article Text |
id | pubmed-7884674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78846742021-02-25 Insulin-like 3 affects zebrafish spermatogenic cells directly and via Sertoli cells Crespo, Diego Assis, Luiz H. C. Zhang, Yu Ting Safian, Diego Furmanek, Tomasz Skaftnesmo, Kai Ove Norberg, Birgitta Ge, Wei Choi, Yung-Ching den Broeder, Marjo J. Legler, Juliette Bogerd, Jan Schulz, Rüdiger W. Commun Biol Article Pituitary hormones can use local signaling molecules to regulate target tissue functions. In adult zebrafish testes, follicle-stimulating hormone (Fsh) strongly increases the production of insulin-like 3 (Insl3), a Leydig cell-derived growth factor found in all vertebrates. Little information is available regarding Insl3 function in adult spermatogenesis. The Insl3 receptors Rxfp2a and 2b were expressed by type A spermatogonia and Sertoli and myoid cells, respectively, in zebrafish testis tissue. Loss of insl3 increased germ cell apoptosis in males starting at 9 months of age, but spermatogenesis appeared normal in fully fertile, younger adults. Insl3 changed the expression of 409 testicular genes. Among others, retinoic acid (RA) signaling was up- and peroxisome proliferator-activated receptor gamma (Pparg) signaling was down-regulated. Follow-up studies showed that RA and Pparg signaling mediated Insl3 effects, resulting in the increased production of differentiating spermatogonia. This suggests that Insl3 recruits two locally active nuclear receptor pathways to implement pituitary (Fsh) stimulation of spermatogenesis. Nature Publishing Group UK 2021-02-15 /pmc/articles/PMC7884674/ /pubmed/33589679 http://dx.doi.org/10.1038/s42003-021-01708-y Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Crespo, Diego Assis, Luiz H. C. Zhang, Yu Ting Safian, Diego Furmanek, Tomasz Skaftnesmo, Kai Ove Norberg, Birgitta Ge, Wei Choi, Yung-Ching den Broeder, Marjo J. Legler, Juliette Bogerd, Jan Schulz, Rüdiger W. Insulin-like 3 affects zebrafish spermatogenic cells directly and via Sertoli cells |
title | Insulin-like 3 affects zebrafish spermatogenic cells directly and via Sertoli cells |
title_full | Insulin-like 3 affects zebrafish spermatogenic cells directly and via Sertoli cells |
title_fullStr | Insulin-like 3 affects zebrafish spermatogenic cells directly and via Sertoli cells |
title_full_unstemmed | Insulin-like 3 affects zebrafish spermatogenic cells directly and via Sertoli cells |
title_short | Insulin-like 3 affects zebrafish spermatogenic cells directly and via Sertoli cells |
title_sort | insulin-like 3 affects zebrafish spermatogenic cells directly and via sertoli cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884674/ https://www.ncbi.nlm.nih.gov/pubmed/33589679 http://dx.doi.org/10.1038/s42003-021-01708-y |
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