FSH signaling pathways in immature granulosa cells that regulate target gene expression: Branching out from protein kinase A

被引:306
作者
Hunzicker-Dunn, Mary
Maizels, Evelyn T.
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Ctr Reprod Sci, Chicago, IL 60611 USA
[3] Northwestern Univ, Feinberg Sch Med, Dept Cell & Mol Biol, Chicago, IL 60611 USA
关键词
follicle-stimulating hormone; mitogen-activated protein kinase; female reproduction; hypoxia-induced factor 1; histone H3; protein kinase A;
D O I
10.1016/j.cellsig.2006.02.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Follicle-stimulating hormone (FSH) is necessary and sufficient to induce maturation of ovarian follicles to a mature, preovulatory phenotype in the intact animal, resulting in the generation of mature eggs and production of estrogen. FSH accomplishes these actions by inducing a complex pattern of gene expression in target granulosa cells that is regulated by input from many different signaling cascades, including those for the extracellular regulated kinases (ERKs), p38 mitogen-activated protein kinases (MAPKs), and phosphatidylinositol-3 kinase (PI3K). The upstream kinase that appears to be responsible for initiating all of the signaling that regulates gene expression in these epithelial cells is protein kinase A (PKA). PKA not only signals to directly phosphorylate transcription factors like CAMP response element binding protein and to promote chromatin remodeling by phosphorylating historic H3, this versatile kinase also enhances the activity of the p38 MAPK, ERK, and PI3K pathways. Additionally, accumulating evidence suggests that activation of a single signaling cascade downstream of PKA is not sufficient to activate target gene expression. Rather, cross-talk between and among signaling cascades is required. We will review the signaling cascades activated by FSH in granulosa cells and how these cascades contribute to the regulation of select target gene expression. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1351 / 1359
页数:9
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