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Permanent Oviduct Posteriorization after Neonatal Exposure to the Phytoestrogen Genistein
Background: Preimplantation embryo loss during oviduct transit has been observed in adult mice after a 5-day neonatal exposure to the phytoestrogen genistein (Gen; 50 mg/kg/day). Objective: We investigated the mechanisms underlying the contribution of the oviduct to infertility. Methods: Female mice...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Institute of Environmental Health Sciences
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226509/ https://www.ncbi.nlm.nih.gov/pubmed/21810550 http://dx.doi.org/10.1289/ehp.1104018 |
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author | Jefferson, Wendy N. Padilla-Banks, Elizabeth Phelps, Jazma Y. Gerrish, Kevin E. Williams, Carmen J. |
author_facet | Jefferson, Wendy N. Padilla-Banks, Elizabeth Phelps, Jazma Y. Gerrish, Kevin E. Williams, Carmen J. |
author_sort | Jefferson, Wendy N. |
collection | PubMed |
description | Background: Preimplantation embryo loss during oviduct transit has been observed in adult mice after a 5-day neonatal exposure to the phytoestrogen genistein (Gen; 50 mg/kg/day). Objective: We investigated the mechanisms underlying the contribution of the oviduct to infertility. Methods: Female mice were treated on postnatal days 1–5 with corn oil or Gen (50 mg/kg/day). We compared morphology, gene expression, and protein expression in different regions of the reproductive tracts of Gen-treated mice with those of control littermates at several time points. Results: Neonatal Gen treatment resulted in substantial changes in expression of genes that modulate neonatal oviduct morphogenesis, including Hoxa (homeobox A cluster), Wnt (wingless-related MMTV integration site), and hedgehog signaling genes. An estrogen receptor antagonist blocked these effects, indicating that they were induced by the estrogenic activity of Gen. Oviducts of adults treated neonatally with Gen had abnormal morphology and were stably “posteriorized,” as indicated by altered Hoxa gene patterning during the time of treatment and dramatic, permanent up-regulation of homeobox genes (e.g., Pitx1, Six1) normally expressed only in the cervix and vagina. Conclusions: Neonatal exposure to estrogenic environmental chemicals permanently disrupts oviduct morphogenesis and adult gene expression patterns, and these changes likely contribute to the infertility phenotype. |
format | Online Article Text |
id | pubmed-3226509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | National Institute of Environmental Health Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-32265092012-01-04 Permanent Oviduct Posteriorization after Neonatal Exposure to the Phytoestrogen Genistein Jefferson, Wendy N. Padilla-Banks, Elizabeth Phelps, Jazma Y. Gerrish, Kevin E. Williams, Carmen J. Environ Health Perspect Research Background: Preimplantation embryo loss during oviduct transit has been observed in adult mice after a 5-day neonatal exposure to the phytoestrogen genistein (Gen; 50 mg/kg/day). Objective: We investigated the mechanisms underlying the contribution of the oviduct to infertility. Methods: Female mice were treated on postnatal days 1–5 with corn oil or Gen (50 mg/kg/day). We compared morphology, gene expression, and protein expression in different regions of the reproductive tracts of Gen-treated mice with those of control littermates at several time points. Results: Neonatal Gen treatment resulted in substantial changes in expression of genes that modulate neonatal oviduct morphogenesis, including Hoxa (homeobox A cluster), Wnt (wingless-related MMTV integration site), and hedgehog signaling genes. An estrogen receptor antagonist blocked these effects, indicating that they were induced by the estrogenic activity of Gen. Oviducts of adults treated neonatally with Gen had abnormal morphology and were stably “posteriorized,” as indicated by altered Hoxa gene patterning during the time of treatment and dramatic, permanent up-regulation of homeobox genes (e.g., Pitx1, Six1) normally expressed only in the cervix and vagina. Conclusions: Neonatal exposure to estrogenic environmental chemicals permanently disrupts oviduct morphogenesis and adult gene expression patterns, and these changes likely contribute to the infertility phenotype. National Institute of Environmental Health Sciences 2011-08-02 2011-11 /pmc/articles/PMC3226509/ /pubmed/21810550 http://dx.doi.org/10.1289/ehp.1104018 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, ?Reproduced with permission from Environmental Health Perspectives?); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright. |
spellingShingle | Research Jefferson, Wendy N. Padilla-Banks, Elizabeth Phelps, Jazma Y. Gerrish, Kevin E. Williams, Carmen J. Permanent Oviduct Posteriorization after Neonatal Exposure to the Phytoestrogen Genistein |
title | Permanent Oviduct Posteriorization after Neonatal Exposure to the Phytoestrogen Genistein |
title_full | Permanent Oviduct Posteriorization after Neonatal Exposure to the Phytoestrogen Genistein |
title_fullStr | Permanent Oviduct Posteriorization after Neonatal Exposure to the Phytoestrogen Genistein |
title_full_unstemmed | Permanent Oviduct Posteriorization after Neonatal Exposure to the Phytoestrogen Genistein |
title_short | Permanent Oviduct Posteriorization after Neonatal Exposure to the Phytoestrogen Genistein |
title_sort | permanent oviduct posteriorization after neonatal exposure to the phytoestrogen genistein |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226509/ https://www.ncbi.nlm.nih.gov/pubmed/21810550 http://dx.doi.org/10.1289/ehp.1104018 |
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