FSH-stimulated PTEN activity accounts for the lack of FSH mitogenic effect in prepubertal rat Sertoli cells

Joëlle Dupont (1) , Astrid Musnier (1) , Jeremy Decourtye (1) , Thomas Boulo (1) , C. Lécureuil (2) , H. Guillou (2) , Sophie Valet (1) , Sophie Fouchécourt (1) , J.L. Pitetti (3) , S. Nef (3) , Eric Reiter (1) , Pascale Crépieux (1)

1 PRC - Physiologie de la reproduction et des comportements [Nouzilly]
2 The Inositide Laboratory
3 Department of Genetic Medicine and Development

Follicle-stimulating hormone (FSH) controls the proliferation and differentiation of Sertoli cells of the testis. FSH binds a G protein-coupled receptor (GPCR) to stimulate downstream effectors of the phosphoinositide-3 kinase (PI3K)-dependent pathway, without enhancing PI3K activity. To clarify this paradox, we explored the activity of phosphatase and tensin homolog deleted in chromosome 10 (PTEN), the PI3K major regulator, in primary cultures of rat Sertoli cells. We show that, within minutes, FSH increases PTEN neo-synthesis, requiring the proteasomal degradation of an unidentified intermediate, as well as PTEN enzymatic activity. Importantly, introducing an antisense cDNA of PTEN into differentiating Sertoli cells restores FSH-dependent cell proliferation. In conclusion, these results provide a new mechanism of PTEN regulation, which could serve to block entry into S phase of Sertoli cells, while they are proceeding through differentiation in prepubertal animals.

Mots clés: sertoli cell; cell differentiation (rat testis); fsh; pten

Domaines: Autre [q-bio.OT]

Joëlle Dupont, Astrid Musnier, Jeremy Decourtye, Thomas Boulo, C. Lécureuil, et al.. FSH-stimulated PTEN activity accounts for the lack of FSH mitogenic effect in prepubertal rat Sertoli cells. Molecular and Cellular Endocrinology, 2010, 315 (1-2), pp.271-276. ⟨10.1016/j.mce.2009.09.016⟩. ⟨hal-01136273⟩