Journal Article

Peroxisome Proliferator-Activated Receptor γ Is a Target for Halogenated Analogs of Bisphenol A

Bourguet, William, Riu, Anne, Perdu, Elisabeth, Zalko, Daniel, Grimaldi, Marina, le Maire, Albane, Balaguer, Patrick, Bey, Gilbert, Phillips, Kevin, Boulahtouf, Abdelhay

2011

Overview

Background: The occurrence of halogenated analogs of the xenoestrogen bisphenol A (BPA) has been recently demonstrated both in environmental and human samples. These analogs include brominated [e.g., tetrabromobisphenol A (TBBPA)] and chlorinated [e.g., tetrachlorobisphenol A (TCBPA) bisphenols, which are both flame retardants. Because of their structural homology with BPA, such chemicals are candidate endocrine disruptors. However, their possible target(s) within the nuclear hormone receptor superfamily has remained unknown. Objectives: We investigated whether BPA and its halogenated analogs could be ligands of estrogen receptors (ERs) and peroxisome proliferator-activated receptors (PPARs) and act as endocrine-disrupting chemicals. Methods: We studied the activity of compounds using reporter cell lines expressing ERs and PPARs. We measured the binding affinities to PPARγ by competitive binding assays with [³H]-rosiglitazone and investigated the impact of TBBPA and TCBPA on adipocyte differentiation using NIH3T3-L1 cells. Finally, we determined the binding mode of halogenated BPAs to PPARγ by X-ray crystallography. Results: We observed that TBBPA and TCBPA are human, zebrafish, and Xenopus PPARγ ligands and determined the mechanism by which these chemicals bind to and activate PPARγ. We also found evidence that activation of ERα, ERß, and PPARγ depends on the degree of halogenation in BPA analogs. We observed that the bulkier brominated BPA analogs, the greater their capability to activate PPARγ and the weaker their estrogenic potential. Conclusions: Our results strongly suggest that polyhalogenated bisphenols could function as obesogens by acting as agonists to disrupt physiological functions regulated by human or animal PPARγ.

• Publisher: National Institute of Environmental Health Sciences,US Department of Health and Human Services
• Subject: Agonists / Animals / Binding, Competitive / Biological and medical sciences / Bisphenol-A / Bisphenols / Business publications audits / Cell Line / Cell lines / Cell receptors / Chemical hazards / Chlorophenols - pharmacology / Crystallography, X-Ray / Endocrine Disruptors - pharmacology / Environment. Living conditions / Environmental health / Estrogen Receptor alpha - genetics / Estrogen Receptor alpha - metabolism / Estrogen Receptor beta - genetics / Estrogen Receptor beta - metabolism / Estrogens, Non-Steroidal - pharmacology / Flame retardants / Flame Retardants - pharmacology / Health aspects / Humans / Life Sciences / Ligands / Ligands (Biochemistry) / Lipogenesis / Medical sciences / Metabolic diseases / Obesity / Polybrominated Biphenyls - pharmacology / PPAR alpha - genetics / PPAR alpha - metabolism / PPAR delta - genetics / PPAR delta - metabolism / PPAR gamma - genetics / PPAR gamma - metabolism / Properties / Public health. Hygiene / Public health. Hygiene-occupational medicine / Receptors / Toxicology / Xenopus - genetics / Xenopus - metabolism / Zebrafish - genetics / Zebrafish - metabolism