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INSL3 in the Ruminant: A Powerful Indicator of Gender- and Genetic-Specific Feto-Maternal Dialogue

The hormone Insulin-like peptide 3 (INSL3) is a major secretory product of the Leydig cells from both fetal and adult testes. Consequently, it is a major gender-specific circulating hormone in the male fetus, where it is responsible for the first phase of testicular descent, and in the adult male. I...

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Autores principales: Anand-Ivell, Ravinder, Hiendleder, Stefan, Viñoles, Carolina, Martin, Graeme B., Fitzsimmons, Carolyn, Eurich, Andrea, Hafen, Bettina, Ivell, Richard
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095623/
https://www.ncbi.nlm.nih.gov/pubmed/21603619
http://dx.doi.org/10.1371/journal.pone.0019821
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author Anand-Ivell, Ravinder
Hiendleder, Stefan
Viñoles, Carolina
Martin, Graeme B.
Fitzsimmons, Carolyn
Eurich, Andrea
Hafen, Bettina
Ivell, Richard
author_facet Anand-Ivell, Ravinder
Hiendleder, Stefan
Viñoles, Carolina
Martin, Graeme B.
Fitzsimmons, Carolyn
Eurich, Andrea
Hafen, Bettina
Ivell, Richard
author_sort Anand-Ivell, Ravinder
collection PubMed
description The hormone Insulin-like peptide 3 (INSL3) is a major secretory product of the Leydig cells from both fetal and adult testes. Consequently, it is a major gender-specific circulating hormone in the male fetus, where it is responsible for the first phase of testicular descent, and in the adult male. In most female mammals, circulating levels are very low, corresponding to only a small production of INSL3 by the mature ovaries. Female ruminants are exceptional in exhibiting high INSL3 gene expression by the thecal cells of antral follicles and by the corpora lutea. We have developed a specific and sensitive immunoassay to measure ruminant INSL3 and show that, corresponding to the high ovarian gene expression, non-pregnant adult female sheep and cows have up to four times the levels observed in other female mammals. Significantly, this level declines during mid-pregnancy in cows carrying a female fetus, in which INSL3 is undetectable. However, in cows carrying a male fetus, circulating maternal INSL3 becomes elevated further, presumably due to the transplacental transfer of fetal INSL3 into the maternal circulation. Within male fetal blood, INSL3 is high in mid-pregnancy (day 153) corresponding to the first transabdominal phase of testicular descent, and shows a marked dependence on paternal genetics, with pure bred or hybrid male fetuses of Bos taurus (Angus) paternal genome having 30% higher INSL3 levels than those of Bos indicus (Brahman) paternity. Thus INSL3 provides the first example of a gender-specific fetal hormone with the potential to influence both placental and maternal physiology.
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spelling pubmed-30956232011-05-19 INSL3 in the Ruminant: A Powerful Indicator of Gender- and Genetic-Specific Feto-Maternal Dialogue Anand-Ivell, Ravinder Hiendleder, Stefan Viñoles, Carolina Martin, Graeme B. Fitzsimmons, Carolyn Eurich, Andrea Hafen, Bettina Ivell, Richard PLoS One Research Article The hormone Insulin-like peptide 3 (INSL3) is a major secretory product of the Leydig cells from both fetal and adult testes. Consequently, it is a major gender-specific circulating hormone in the male fetus, where it is responsible for the first phase of testicular descent, and in the adult male. In most female mammals, circulating levels are very low, corresponding to only a small production of INSL3 by the mature ovaries. Female ruminants are exceptional in exhibiting high INSL3 gene expression by the thecal cells of antral follicles and by the corpora lutea. We have developed a specific and sensitive immunoassay to measure ruminant INSL3 and show that, corresponding to the high ovarian gene expression, non-pregnant adult female sheep and cows have up to four times the levels observed in other female mammals. Significantly, this level declines during mid-pregnancy in cows carrying a female fetus, in which INSL3 is undetectable. However, in cows carrying a male fetus, circulating maternal INSL3 becomes elevated further, presumably due to the transplacental transfer of fetal INSL3 into the maternal circulation. Within male fetal blood, INSL3 is high in mid-pregnancy (day 153) corresponding to the first transabdominal phase of testicular descent, and shows a marked dependence on paternal genetics, with pure bred or hybrid male fetuses of Bos taurus (Angus) paternal genome having 30% higher INSL3 levels than those of Bos indicus (Brahman) paternity. Thus INSL3 provides the first example of a gender-specific fetal hormone with the potential to influence both placental and maternal physiology. Public Library of Science 2011-05-16 /pmc/articles/PMC3095623/ /pubmed/21603619 http://dx.doi.org/10.1371/journal.pone.0019821 Text en Anand-Ivell et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Anand-Ivell, Ravinder
Hiendleder, Stefan
Viñoles, Carolina
Martin, Graeme B.
Fitzsimmons, Carolyn
Eurich, Andrea
Hafen, Bettina
Ivell, Richard
INSL3 in the Ruminant: A Powerful Indicator of Gender- and Genetic-Specific Feto-Maternal Dialogue
title INSL3 in the Ruminant: A Powerful Indicator of Gender- and Genetic-Specific Feto-Maternal Dialogue
title_full INSL3 in the Ruminant: A Powerful Indicator of Gender- and Genetic-Specific Feto-Maternal Dialogue
title_fullStr INSL3 in the Ruminant: A Powerful Indicator of Gender- and Genetic-Specific Feto-Maternal Dialogue
title_full_unstemmed INSL3 in the Ruminant: A Powerful Indicator of Gender- and Genetic-Specific Feto-Maternal Dialogue
title_short INSL3 in the Ruminant: A Powerful Indicator of Gender- and Genetic-Specific Feto-Maternal Dialogue
title_sort insl3 in the ruminant: a powerful indicator of gender- and genetic-specific feto-maternal dialogue
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095623/
https://www.ncbi.nlm.nih.gov/pubmed/21603619
http://dx.doi.org/10.1371/journal.pone.0019821
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