Dépôt numérique
RECHERCHER

A Unique Co-culture Model for Fundamental and Applied Studies of Human Fetoplacental Steroidogenesis and Interference by Environmental Chemicals

Téléchargements

Téléchargements par mois depuis la dernière année

Thibeault, Andrée-Anne; Deroy, Kathy; Vaillancourt, Cathy et Sanderson, J. Thomas (2014). A Unique Co-culture Model for Fundamental and Applied Studies of Human Fetoplacental Steroidogenesis and Interference by Environmental Chemicals Environmental Health Perspectives , vol. 122 , nº 4. pp. 371-7. DOI: 10.1289/ehp.1307518.

[thumbnail of Reproduced with permission from Environmental Health Perspectives]
Prévisualisation
PDF (Reproduced with permission from Environmental Health Perspectives) - Version publiée
Disponible sous licence Creative Commons Attribution Non-commercial.

Télécharger (412kB) | Prévisualisation

Résumé

Background: Experimental tools for studying the complex steroidogenic interactions that occur between placenta and fetus during human pregnancy are extremely limited.Objectives: We aimed to develop a co-culture model to study steroidogenesis by the human fetoplacental unit and its disruption by exposure to environmental contaminants.Methods: We cultured BeWo human choriocarcinoma cells, representing the villous cytotrophoblast, and H295R human adrenocortical carcinoma cells, representing the fetal unit, in a carefully adapted co-culture medium. We placed H295R cells in 24-well plates and BeWo cells on transwell inserts with or without pesticide treatment (atrazine or prochloraz) and assessed CYP19 activity and hormonal production after 24 hr of co-culture.Results: The co-culture exhibited the steroidogenic profile of the fetoplacental unit, allowing a synergistic production of estradiol and estriol (but not of estrone) of 133.3 +/- 11.3 pg/mL and 440.8 +/- 44.0 pg/mL, respectively. Atrazine and prochloraz had cell-type specific effects on CYP19 activity and estrogen production in co-culture. Atrazine induced CYP19 activity and estrogen production in H295R cells only, but did not affect overall estrogen production in co-culture, whereas prochloraz inhibited CYP19 activity exclusively in BeWo cells and reduced estrogen production in co-culture by almost 90%. In contrast, prochloraz did not affect estradiol or estrone production in BeWo cells in monoculture. These differential effects underline the relevance of our co-culture approach to model fetoplacental steroidogenesis.Conclusions: The co-culture of H295R and BeWo cells creates a unique in vitro model to reproduce the steroidogenic cooperation between fetus and placenta during pregnancy and can be used to study the endocrine-disrupting effects of environmental chemicals.Citation: Hudon Thibeault AA, Deroy K, Vaillancourt C, Sanderson JT. 2014. A unique co-culture model for fundamental and applied studies of human fetoplacental steroidogenesis and interference by environmental chemicals. Environ Health Perspect 122:371-377; http://dx.doi.org/10.1289/ehp.1307518.

Type de document: Article
Mots-clés libres: -
Centre: Centre INRS-Institut Armand Frappier
Date de dépôt: 23 mars 2016 19:46
Dernière modification: 05 juill. 2017 14:53
URI: https://espace.inrs.ca/id/eprint/3125

Gestion Actions (Identification requise)

Modifier la notice Modifier la notice