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Cadmium Increases Human Fetal Germ Cell Apoptosis
BACKGROUND: Cadmium (Cd) is a common environmental pollutant and a major constituent of tobacco smoke. Adverse effects of this heavy metal on reproductive function have been identified in adults; however, no studies have examined its effects on human reproductive organs during development. OBJECTIVE...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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National Institute of Environmental Health Sciences
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854759/ https://www.ncbi.nlm.nih.gov/pubmed/20064782 http://dx.doi.org/10.1289/ehp.0900975 |
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author | Angenard, Gaëlle Muczynski, Vincent Coffigny, Hervé Pairault, Catherine Duquenne, Clotilde Frydman, René Habert, René Rouiller-Fabre, Virginie Livera, Gabriel |
author_facet | Angenard, Gaëlle Muczynski, Vincent Coffigny, Hervé Pairault, Catherine Duquenne, Clotilde Frydman, René Habert, René Rouiller-Fabre, Virginie Livera, Gabriel |
author_sort | Angenard, Gaëlle |
collection | PubMed |
description | BACKGROUND: Cadmium (Cd) is a common environmental pollutant and a major constituent of tobacco smoke. Adverse effects of this heavy metal on reproductive function have been identified in adults; however, no studies have examined its effects on human reproductive organs during development. OBJECTIVES: Using our previously developed organ culture system, we investigated the effects of cadmium chloride on human gonads at the beginning of fetal life, a critical stage in the development of reproductive function. METHODS: Human fetal gonads were recovered during the first trimester (7–11 weeks postconception) and cultured with or without Cd. We used different concentrations of Cd and compared results with those obtained with mouse fetal gonads at similar stages. RESULTS: Cd, at concentrations as low as 1 μM, significantly decreased the germ cell density in human fetal ovaries. This correlated with an increase in germ cell apoptosis, but there was no effect on proliferation. Similarly, in the human fetal testis, Cd (1 μM) reduced germ cell number without affecting testosterone secretion. In mouse fetal gonads, Cd increased only female germ cell apoptosis. CONCLUSIONS: This is the first experimental demonstration that Cd, at low concentrations, alters the survival of male and female germ cells in humans. Considering data demonstrating extensive human exposure, we believe that current environmental levels of Cd could be deleterious to early gametogenesis. |
format | Text |
id | pubmed-2854759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | National Institute of Environmental Health Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-28547592010-04-26 Cadmium Increases Human Fetal Germ Cell Apoptosis Angenard, Gaëlle Muczynski, Vincent Coffigny, Hervé Pairault, Catherine Duquenne, Clotilde Frydman, René Habert, René Rouiller-Fabre, Virginie Livera, Gabriel Environ Health Perspect Research BACKGROUND: Cadmium (Cd) is a common environmental pollutant and a major constituent of tobacco smoke. Adverse effects of this heavy metal on reproductive function have been identified in adults; however, no studies have examined its effects on human reproductive organs during development. OBJECTIVES: Using our previously developed organ culture system, we investigated the effects of cadmium chloride on human gonads at the beginning of fetal life, a critical stage in the development of reproductive function. METHODS: Human fetal gonads were recovered during the first trimester (7–11 weeks postconception) and cultured with or without Cd. We used different concentrations of Cd and compared results with those obtained with mouse fetal gonads at similar stages. RESULTS: Cd, at concentrations as low as 1 μM, significantly decreased the germ cell density in human fetal ovaries. This correlated with an increase in germ cell apoptosis, but there was no effect on proliferation. Similarly, in the human fetal testis, Cd (1 μM) reduced germ cell number without affecting testosterone secretion. In mouse fetal gonads, Cd increased only female germ cell apoptosis. CONCLUSIONS: This is the first experimental demonstration that Cd, at low concentrations, alters the survival of male and female germ cells in humans. Considering data demonstrating extensive human exposure, we believe that current environmental levels of Cd could be deleterious to early gametogenesis. National Institute of Environmental Health Sciences 2010-03 2009-10-14 /pmc/articles/PMC2854759/ /pubmed/20064782 http://dx.doi.org/10.1289/ehp.0900975 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 Angenard, Gaëlle Muczynski, Vincent Coffigny, Hervé Pairault, Catherine Duquenne, Clotilde Frydman, René Habert, René Rouiller-Fabre, Virginie Livera, Gabriel Cadmium Increases Human Fetal Germ Cell Apoptosis |
title | Cadmium Increases Human Fetal Germ Cell Apoptosis |
title_full | Cadmium Increases Human Fetal Germ Cell Apoptosis |
title_fullStr | Cadmium Increases Human Fetal Germ Cell Apoptosis |
title_full_unstemmed | Cadmium Increases Human Fetal Germ Cell Apoptosis |
title_short | Cadmium Increases Human Fetal Germ Cell Apoptosis |
title_sort | cadmium increases human fetal germ cell apoptosis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854759/ https://www.ncbi.nlm.nih.gov/pubmed/20064782 http://dx.doi.org/10.1289/ehp.0900975 |
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