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In Vitro Effects of the Endocrine Disruptor p,p’-DDT on Human Follitropin Receptor
BACKGROUND: 1-chloro-4-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene (p,p′-DDT) is a persistent environmental endocrine disruptor (ED). Several studies have shown an association between p,p′-DDT exposure and reproductive abnormalities. OBJECTIVES: To investigate the putative effects of p,p′-DDT o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Institute of Environmental Health Sciences
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937862/ https://www.ncbi.nlm.nih.gov/pubmed/26895433 http://dx.doi.org/10.1289/ehp.1510006 |
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author | Munier, Mathilde Grouleff, Julie Gourdin, Louis Fauchard, Mathilde Chantreau, Vanessa Henrion, Daniel Coutant, Régis Schiøtt, Birgit Chabbert, Marie Rodien, Patrice |
author_facet | Munier, Mathilde Grouleff, Julie Gourdin, Louis Fauchard, Mathilde Chantreau, Vanessa Henrion, Daniel Coutant, Régis Schiøtt, Birgit Chabbert, Marie Rodien, Patrice |
author_sort | Munier, Mathilde |
collection | PubMed |
description | BACKGROUND: 1-chloro-4-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene (p,p′-DDT) is a persistent environmental endocrine disruptor (ED). Several studies have shown an association between p,p′-DDT exposure and reproductive abnormalities. OBJECTIVES: To investigate the putative effects of p,p′-DDT on the human follitropin receptor (FSHR) function. METHODS: and Results: We used Chinese hamster ovary (CHO) cells stably expressing human FSHR to investigate the impact of p,p′-DDT on FSHR activity and its interaction with the receptor. At a concentration of 5 μM p,p′-DDT increased the maximum response of the FSHR to follitropin by 32 ± 7.45%. However, 5 μM p,p′-DDT decreased the basal activity and did not influence the maximal response of the closely related LH/hCG receptor to human chorionic gonadotropin (hCG). The potentiating effect of p,p′-DDT was specific for the FSHR. Moreover, in cells that did not express FSHR, p,p′-DDT had no effect on cAMP response. Thus, the potentiating effect of p,p′-DDT was dependent on the FSHR. In addition, p,p′-DDT increased the sensitivity of FSHR to hCG and to a low molecular weight agonist of the FSHR, 3-((5methyl)-2-(4-benzyloxy-phenyl)-5-{[2-[3-ethoxy-4-methoxy-phenyl)-ethylcarbamoyl]-methyl}-4-oxo-thiazolidin-3-yl)-benzamide (16a). Basal activity in response to p,p′-DDT and potentiation of the FSHR response to FSH by p,p′-DDT varied among FSHR mutants with altered transmembrane domains (TMDs), consistent with an effect of p,p′-DDT via TMD binding. This finding was corroborated by the results of simultaneously docking p,p′-DDT and 16a into the FSHR transmembrane bundle. CONCLUSION: p,p′-DDT acted as a positive allosteric modulator of the FSHR in our experimental model. These findings suggest that G protein–coupled receptors are additional targets of endocrine disruptors. CITATION: Munier M, Grouleff J, Gourdin L, Fauchard M, Chantreau V, Henrion D, Coutant R, Schiøtt B, Chabbert M, Rodien P. 2016. In vitro effects of the endocrine disruptor p,p′-DDT on human follitropin receptor. Environ Health Perspect 124:991–999; http://dx.doi.org/10.1289/ehp.1510006 |
format | Online Article Text |
id | pubmed-4937862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | National Institute of Environmental Health Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-49378622016-07-13 In Vitro Effects of the Endocrine Disruptor p,p’-DDT on Human Follitropin Receptor Munier, Mathilde Grouleff, Julie Gourdin, Louis Fauchard, Mathilde Chantreau, Vanessa Henrion, Daniel Coutant, Régis Schiøtt, Birgit Chabbert, Marie Rodien, Patrice Environ Health Perspect Research BACKGROUND: 1-chloro-4-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene (p,p′-DDT) is a persistent environmental endocrine disruptor (ED). Several studies have shown an association between p,p′-DDT exposure and reproductive abnormalities. OBJECTIVES: To investigate the putative effects of p,p′-DDT on the human follitropin receptor (FSHR) function. METHODS: and Results: We used Chinese hamster ovary (CHO) cells stably expressing human FSHR to investigate the impact of p,p′-DDT on FSHR activity and its interaction with the receptor. At a concentration of 5 μM p,p′-DDT increased the maximum response of the FSHR to follitropin by 32 ± 7.45%. However, 5 μM p,p′-DDT decreased the basal activity and did not influence the maximal response of the closely related LH/hCG receptor to human chorionic gonadotropin (hCG). The potentiating effect of p,p′-DDT was specific for the FSHR. Moreover, in cells that did not express FSHR, p,p′-DDT had no effect on cAMP response. Thus, the potentiating effect of p,p′-DDT was dependent on the FSHR. In addition, p,p′-DDT increased the sensitivity of FSHR to hCG and to a low molecular weight agonist of the FSHR, 3-((5methyl)-2-(4-benzyloxy-phenyl)-5-{[2-[3-ethoxy-4-methoxy-phenyl)-ethylcarbamoyl]-methyl}-4-oxo-thiazolidin-3-yl)-benzamide (16a). Basal activity in response to p,p′-DDT and potentiation of the FSHR response to FSH by p,p′-DDT varied among FSHR mutants with altered transmembrane domains (TMDs), consistent with an effect of p,p′-DDT via TMD binding. This finding was corroborated by the results of simultaneously docking p,p′-DDT and 16a into the FSHR transmembrane bundle. CONCLUSION: p,p′-DDT acted as a positive allosteric modulator of the FSHR in our experimental model. These findings suggest that G protein–coupled receptors are additional targets of endocrine disruptors. CITATION: Munier M, Grouleff J, Gourdin L, Fauchard M, Chantreau V, Henrion D, Coutant R, Schiøtt B, Chabbert M, Rodien P. 2016. In vitro effects of the endocrine disruptor p,p′-DDT on human follitropin receptor. Environ Health Perspect 124:991–999; http://dx.doi.org/10.1289/ehp.1510006 National Institute of Environmental Health Sciences 2016-02-19 2016-07 /pmc/articles/PMC4937862/ /pubmed/26895433 http://dx.doi.org/10.1289/ehp.1510006 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 Munier, Mathilde Grouleff, Julie Gourdin, Louis Fauchard, Mathilde Chantreau, Vanessa Henrion, Daniel Coutant, Régis Schiøtt, Birgit Chabbert, Marie Rodien, Patrice In Vitro Effects of the Endocrine Disruptor p,p’-DDT on Human Follitropin Receptor |
title |
In Vitro Effects of the Endocrine Disruptor p,p’-DDT on Human Follitropin Receptor |
title_full |
In Vitro Effects of the Endocrine Disruptor p,p’-DDT on Human Follitropin Receptor |
title_fullStr |
In Vitro Effects of the Endocrine Disruptor p,p’-DDT on Human Follitropin Receptor |
title_full_unstemmed |
In Vitro Effects of the Endocrine Disruptor p,p’-DDT on Human Follitropin Receptor |
title_short |
In Vitro Effects of the Endocrine Disruptor p,p’-DDT on Human Follitropin Receptor |
title_sort | in vitro effects of the endocrine disruptor p,p’-ddt on human follitropin receptor |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937862/ https://www.ncbi.nlm.nih.gov/pubmed/26895433 http://dx.doi.org/10.1289/ehp.1510006 |
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