Author
Listed:
- Vanessa Delfosse
(Inserm U1054
CNRS UMR5048, Centre de Biochimie Structurale
Université de Montpellier)
- Béatrice Dendele
(Université de Montpellier
IRCM, Institut de Recherche en Cancérologie de Montpellier
Inserm, U1194
ICM, Institut régional du Cancer de Montpellier)
- Tiphaine Huet
(Inserm U1054
CNRS UMR5048, Centre de Biochimie Structurale
Université de Montpellier)
- Marina Grimaldi
(Université de Montpellier
IRCM, Institut de Recherche en Cancérologie de Montpellier
Inserm, U1194
ICM, Institut régional du Cancer de Montpellier)
- Abdelhay Boulahtouf
(Université de Montpellier
IRCM, Institut de Recherche en Cancérologie de Montpellier
Inserm, U1194
ICM, Institut régional du Cancer de Montpellier)
- Sabine Gerbal-Chaloin
(Université de Montpellier
Inserm U1040)
- Bertrand Beucher
(Université de Montpellier
Inserm U661
CNRS UMR5203, Institut de Génomique Fonctionnelle)
- Dominique Roecklin
(NovAliX)
- Christina Muller
(NovAliX)
- Roger Rahmani
(INRA UMR 1331, TOXALIM)
- Vincent Cavaillès
(Université de Montpellier
IRCM, Institut de Recherche en Cancérologie de Montpellier
Inserm, U1194
ICM, Institut régional du Cancer de Montpellier)
- Martine Daujat-Chavanieu
(Université de Montpellier
Inserm U1040
CHU de Montpellier, Institut de Recherche en Biothérapie)
- Valérie Vivat
(NovAliX)
- Jean-Marc Pascussi
(Université de Montpellier
Inserm U661
CNRS UMR5203, Institut de Génomique Fonctionnelle)
- Patrick Balaguer
(Université de Montpellier
IRCM, Institut de Recherche en Cancérologie de Montpellier
Inserm, U1194
ICM, Institut régional du Cancer de Montpellier)
- William Bourguet
(Inserm U1054
CNRS UMR5048, Centre de Biochimie Structurale
Université de Montpellier)
Abstract
Humans are chronically exposed to multiple exogenous substances, including environmental pollutants, drugs and dietary components. Many of these compounds are suspected to impact human health, and their combination in complex mixtures could exacerbate their harmful effects. Here we demonstrate that a pharmaceutical oestrogen and a persistent organochlorine pesticide, both exhibiting low efficacy when studied separately, cooperatively bind to the pregnane X receptor, leading to synergistic activation. Biophysical analysis shows that each ligand enhances the binding affinity of the other, so the binary mixture induces a substantial biological response at doses at which each chemical individually is inactive. High-resolution crystal structures reveal the structural basis for the observed cooperativity. Our results suggest that the formation of ‘supramolecular ligands’ within the ligand-binding pocket of nuclear receptors contributes to the synergistic toxic effect of chemical mixtures, which may have broad implications for the fields of endocrine disruption, toxicology and chemical risk assessment.
Suggested Citation
Vanessa Delfosse & Béatrice Dendele & Tiphaine Huet & Marina Grimaldi & Abdelhay Boulahtouf & Sabine Gerbal-Chaloin & Bertrand Beucher & Dominique Roecklin & Christina Muller & Roger Rahmani & Vincent, 2015.
"Synergistic activation of human pregnane X receptor by binary cocktails of pharmaceutical and environmental compounds,"
Nature Communications, Nature, vol. 6(1), pages 1-10, November.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms9089
DOI: 10.1038/ncomms9089
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Citations
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Cited by:
- Efren Garcia-Maldonado & Andrew D. Huber & Sergio C. Chai & Stanley Nithianantham & Yongtao Li & Jing Wu & Shyaron Poudel & Darcie J. Miller & Jayaraman Seetharaman & Taosheng Chen, 2024.
"Chemical manipulation of an activation/inhibition switch in the nuclear receptor PXR,"
Nature Communications, Nature, vol. 15(1), pages 1-14, December.
- Nicole Bijlsma & Marc M. Cohen, 2016.
"Environmental Chemical Assessment in Clinical Practice: Unveiling the Elephant in the Room,"
IJERPH, MDPI, vol. 13(2), pages 1-27, February.
- Jiabao Liu & Ainaz Malekoltojari & Anjana Asokakumar & Vimanda Chow & Linhao Li & Hao Li & Marina Grimaldi & Nathanlown Dang & Jhenielle Campbell & Holly Barrett & Jianxian Sun & William Navarre & Der, 2024.
"Diindoles produced from commensal microbiota metabolites function as endogenous CAR/Nr1i3 ligands,"
Nature Communications, Nature, vol. 15(1), pages 1-12, December.
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