Carbon Black Nanoparticles Inhibit Aromatase Expression and Estradiol Secretion in Human Granulosa Cells Through the ERK1/2 Pathway

Author:

Simon Violaine1,Avet Charlotte1,Grange-Messent Valérie2,Wargnier Richard1,Denoyelle Chantal1,Pierre Alice1,Dairou Julien3,Dupret Jean-Marie3,Cohen-Tannoudji Joëlle1

Affiliation:

1. Sorbonne Paris Cité, Université Paris-Diderot, Centre National de la Recherche Scientifique (CNRS) Unité Mixte de Recherche (UMR) 8251, Institut National de la Santé et de la Recherche Médicale (INSERM) U1133, Biologie Fonctionnelle et Adaptative, Physiologie de l’axe gonadotrope, Paris 75013, France

2. Sorbonne Universités, Université Pierre et Marie Curie UM CR18, CNRS UMR 8246, INSERM U1130, Neuroscience Paris Seine, Neuroplasticité des Comportements de Reproduction, Paris 75005, France

3. Sorbonne Paris Cité, Université Paris-Diderot, CNRS, Biologie Fonctionnelle et Adaptative UMR 8251, Réponses Moléculaires et Cellulaires aux Xénobiotiques, Paris 75013, France

Abstract

Abstract Secretion of 17-β-estradiol (E2) by human granulosa cells can be disrupted by various environmental toxicants. In the current study, we investigated whether carbon black nanoparticles (CB NPs) affect the steroidogenic activity of cultured human granulosa cells. The human granulosa cell line KGN and granulosa cells from patients undergoing in vitro fertilization were treated with increasing concentrations of CB NPs (1 to 100 µg/mL) together or not with follicle-stimulating hormone (FSH). We observed that CB NPs are internalized in KGN cells without affecting cell viability. CB NPs could be localized in the cytoplasm, within mitochondria and in association with the outer face of the endoplasmic reticulum membrane. In both cell types, CB NPs reduced in a dose-dependent manner the activity of aromatase enzyme, as reflected by a decrease in E2 secretion. A significant decrease was observed in response to CB NPs concentrations from 25 and 50 µg/mL in KGN cell line and primary cultures, respectively. Furthermore, CB NPs decreased aromatase protein levels in both cells and reduced aromatase transcript levels in KGN cells. CB NPs rapidly activated extracellular signal-regulated kinase 1 and 2 in KGN cells and pharmacological inhibition of this signaling pathway using PD 98059 significantly attenuated the inhibitory effects of CB NPs on CYP19A1 gene expression and aromatase activity. CB NPs also inhibited the stimulatory effect of FSH on aromatase expression and activity. Altogether, our study on cultured ovarian granulosa cells reveals that CB NPs decrease estrogens production and highlights possible detrimental effect of these common NPs on female reproductive health.

Publisher

The Endocrine Society

Subject

Endocrinology

Reference60 articles.

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