Abstract
Toxic effects of nanoparticles on female reproductive health have been documented but the underlying mechanisms still need to be clarified. Here, we investigated the effect of carbon black nanoparticles (CB NPs) on the pituitary gonadotropins, luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which are key regulators of gonadal gametogenesis and steroidogenesis. To that purpose, we subjected adult female mice to a weekly non-surgical intratracheal administration of CB NPs at an occupationally relevant dose over 4 weeks. We also analyzed the effects of CB NPs in vitro, using both primary cultures of pituitary cells and the LβT2 gonadotrope cell line. We report here that exposure to CB NPs does not disrupt estrous cyclicity but increases both circulating FSH levels and pituitary FSH β-subunit gene (Fshb) expression in female mice without altering circulating LH levels. Similarly, treatment of anterior pituitary or gonadotrope LβT2 cells with increasing concentrations of CB NPs dose-dependently up-regulates FSH but not LH gene expression or release. Moreover, CB NPs enhance the stimulatory effect of GnRH on Fshb expression in LβT2 cells without interfering with LH regulation. We provide evidence that CB NPs are internalized by LβT2 cells and rapidly activate the cAMP/PKA pathway. We further show that pharmacological inhibition of PKA significantly attenuates the stimulatory effect of CB NPs on Fshb expression. Altogether, our study demonstrates that exposure to CB NPs alters FSH but not LH expression and may thus lead to gonadotropin imbalance.
Highlights
Reproductive processes in mammals are dependent on the appropriate regulation of the synthesis and release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) by the gonadotrope cells of the anterior pituitary
We report that CB NPs increase FSH synthesis and release by pituitary gonadotrope cells both in vivo in female mice and in vitro in rat cultured pituitary cells, as well as in the gonadotrope cell line LβT2
Because the dose of CB NPs used in our study was occupationally relevant (Sanfins et al, 2011; Bourdon et al, 2013), our results underline the fact that exposure to CB NPs may be detrimental for female reproductive health
Summary
Reproductive processes in mammals are dependent on the appropriate regulation of the synthesis and release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) by the gonadotrope cells of the anterior pituitary. These two hormones, act in a concerted manner to regulate gonadal hormone synthesis and gametogenesis in both males and females. GnRH notably triggers the activation of phospholipase Cβ, the mobilization of intracellular calcium and the increase of Protein Kinase C (PKC) activity, leading notably to the activation of the mitogen-activated protein kinase (MAPK) pathways (Naor and Huhtaniemi, 2013). All PKC, PKA and MAPK pathways contribute to the GnRH-stimulated transcription of gonadotropin genes (Thackray et al, 2010)
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