Doctoral thesis (Dissertations and theses)
In vitro study of the impacts of exposure to mixtures of endocrine disrupting chemicals on the aryl hydrocarbon and steroid receptor transcriptional activity
Doan, Thi-Que
2020
 

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Keywords :
Aryl hydrocarbon receptor; CALUX assays; mixture effect; steroid receptors; human exposure; contaminants
Abstract :
[en] Chemicals are undoubtedly important and beneficial for our modern life. As a result, we are exposed to mixtures of chemicals in our daily life through applying them for food production and preservation and for supporting human and animal health and recreation. However, risk assessment for the consumer is usually based on a chemical-by-chemical approach. Among these chemicals, endocrine disruptors (EDs) are of concern, in particular because they are able to alter the function(s) of the endocrine system, leading to adverse health effects in organism or (sub) population levels. In vitro Chemically Activated LUciferase gene eXpression (CALUX) assays involving several transgenic reporter cell lines are interesting tools to study the impacts of exposure to mixtures of EDs and their components on the transcriptional activity of the master xenobiotic receptor, which is the aryl hydrocarbon receptor (AhR), as well as the steroid (estrogen (ER), androgen (AR), progesterone (PR), and glucocorticoid (GR)) receptors. Three mixtures were being investigated as examples of compound groups of human everyday exposure to chemicals: (1) the “total POP mixture” consisting of 29 POPs (persistent organic pollutants) prevalent in Scandinavian human blood, (2) the “ED mixture” containing 18 potential EDs dominantly found in Wallonia raw water intended for drinking water production, and (3) the “polyphenol mixture” containing seven food-based polyphenols. The concentration of each component in the mixture was based on human-relevant exposure such as fold human blood level (the POP mixture), fold maximum quantified concentration in raw water (the ED mixture), or fold recommended intake dose from food supplements (the polyphenol mixture). Specific aims of the project were: (a) evaluating species (rat and human) and/or tissue-specific (hepatocytes and mammary gland) AhR responses to the POP mixture and the polyphenol mixture and their components, (b) profiling the endocrine disrupting activities of the EDs and the mixture thereof prevalent in raw water using AhR and steroid receptors, (c) identifying interactions among the chemicals (additive, antagonistic or synergic effects) on the transcriptional activity of the receptors, (d) identifying the actual chemical(s) the most active in the mixtures, and (e) predicting the effect of the mixtures based on the activity of single compounds. The results showed that 16 out of 29 POPs contaminating human blood were AhR antagonists. The total POP mixture also showed an AhR antagonistic activity although it contained each compound at the concentration below its lowest-observed-effect concentration (LOEC). Chlorinated compounds were the drivers of the activity of the total POP mixture, among which PCB-118 and PCB-138 contributed for 90% of the total POP mixture effect. From the 18 EDs prevalent in raw water, chlorpyrifos, bisphenol A, fluoranthene, phenanthrene, and benzo(a)pyrene demonstrated significant activities on several receptors. Noticeably, benzo(a)pyrene mixed with dioxin TCCD induced a synergistic response in AhR- i reporter human mammary gland cells (DR-T47-D), 10-fold higher than the cells’ response to TCDD alone, at a concentration which could be a realistic blood level after a food contamination incident or in a high exposed sub-population. The mixture of the 18 EDs compounds exerted AhR and ER agonistic activities, which can be explained by the activities of benzo(a)pyrene and bisphenol A in the mixture. While the rat AhR reporter cells (DR-H4IIE) was more sensitive to POP exposure, we showed for the first time that the AhR endogenous ligand FICZ, a tryptophan derivative was more potent than TCDD in the human AhR (DR- HepG2) (40 times more potent than TCDD) while both exhibited a similar potency in the rat cells (after 6h exposure). Two isoflavones (daidzein and genistein) induced a higher AhR agonistic/synergistic activity in the rat cells, while the others (a flavonol (quercetin) and two flavones (baicalin and chrysin), curcumin, and the mixture of the seven polyphenols) caused a stronger AhR antagonistic response in the human cells. Quercetin and resveratrol were the strongest AhR antagonists in the human cells, which contributed most for the antagonistic activity of the polyphenol mixture. Dose-response curves were predicted successfully by concentration addition and general concentration addition models for the POP mixture, while both concentration addition and independent action performed well for estimating the effect of the polyphenol mixture, indicating the additive activity of the components in these mixtures. The results suggested that the endocrine disrupting activities of chemicals in human daily life exposure could involve more than one mechanism: their (anta-) agonistic effects on different receptors with the potential for additive, inhibitory or synergistic effects of mixtures thereof should be considered in risk assessment.
Research center :
FARAH - Fundamental and Applied Research for Animals and Health - ULiège
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Doan, Thi-Que ;  Université de Liège - ULiège > Département de sciences des denrées alimentaires (DDA) > Analyse des denrées alimentaires
Language :
English
Title :
In vitro study of the impacts of exposure to mixtures of endocrine disrupting chemicals on the aryl hydrocarbon and steroid receptor transcriptional activity
Defense date :
24 April 2020
Number of pages :
200
Institution :
ULiège - Université de Liège
Degree :
Doctor of Philosophy in Biochemistry
Promotor :
Scippo, Marie-Louise  ;  Université de Liège - ULiège > Fundamental and Applied Research for Animals and Health (FARAH) > FARAH: Santé publique vétérinaire
Muller, Marc  ;  Université de Liège - ULiège > GIGA > GIGA I3 - Laboratory for Organogenesis and Regeneration
President :
Struman, Ingrid  ;  Université de Liège - ULiège > Département des sciences de la vie
Secretary :
Jury member :
Joaquim-Justo, Célia ;  Université de Liège - ULiège > Freshwater and OCeanic science Unit of reSearch (FOCUS)
Dommes, Jacques ;  Université de Liège - ULiège > Département des sciences de la vie > Biologie végétale translationnelle
Connolly, Lisa
Elskens, Marc
European Projects :
H2020 - 722634 - PROTECTED - PROTECTion against Endocrine Disruptors; Detection, mixtures, health effects, risk assessment and communication.
Name of the research project :
PROTECTion against Endocrine Disruptors; Detection, mixtures, health effects, risk assessment and communication
Funders :
Horizon 2020 Marie Skłodowska-Curie
CE - Commission Européenne [BE]
Commentary :
NA
Available on ORBi :
since 27 April 2020

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