Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8477155 | Molecular and Cellular Endocrinology | 2014 | 9 Pages |
Abstract
The single nucleotide polymorphism p.N680S of the follicle-stimulating hormone (FSH) receptor (FSHR) is a discrete marker of ovarian response but previous in vitro studies failed to demonstrate differences in the response to FSH between N and S carrier cells. Here we demonstrate that p.N680S mediates different kinetics of the response to FSH in vitro. Intracellular cAMP production is faster in p.N680S N than in S homozygous human granulosa cells (45 versus 90 min to achieve the plateau, respectively; Mann-Whitney's U-test; p < 0.005; n = 4). Reflecting the cAMP kinetics, phospho-ERK1/2 and -CREB activation, AREG and STARD1 gene expressions and progesterone production were qualitatively and quantitatively different in N versus S homozygous cells. Finally, the blockade of ERK pathway by U0126 abolishes the genotype-mediated different effects on gene expression and progesterone production (Mann-Whitney's U-test; p ⩾ 0.005; n = 3).
Keywords
COS7GPCRCREBHEK293FSHRpKaIBMX3-isobutyl-1-methylxanthineERK1/2G-protein coupled receptorMAPKStarhuman embryonic kidney 293 cellsgranulosa cellsMEKfollicle-stimulating hormoneFSHcAMP-responsive element binding proteinSteroidogenic acute regulatory proteinprotein kinase Amitogen-activated protein kinasePolymorphismSingle nucleotide polymorphismSNPKinaseextracellular signal-regulated kinaseFSH receptor
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Authors
Livio Casarini, Valeria Moriondo, Marco Marino, Francesca Adversi, Francesco Capodanno, Chiarina Grisolia, Antonio La Marca, Giovanni Battista La Sala, Manuela Simoni,