Rapid signaling mechanisms of estrogens in the developing cerebellum

被引:31
作者
Belcher, Scott M. [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Pharmacol & Cell Biophys, Cincinnati, OH 45267 USA
关键词
cerebellum; development; ERK; estrogen; non-genomic; signal transduction;
D O I
10.1016/j.brainresrev.2007.07.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The steroid hormone 17 beta-estradiol regulates the normal function and development of the mammalian nervous system. Many of estradiol's effects are mediated via the nuclear hormone estrogen receptors ER alpha and ER beta. In addition to regulating estrogen-responsive gene expression, estradiol also acts in an immediate and cell-specific fashion to regulate various intracellular signal transduction pathways. The goal of this review is to develop a contextual framework to understand the generalized function of estrogen during development of brain regions not known to be sexually specialized. However, it is first important to build this framework on the more well-developed foundation of estrogen's gonad-driven sex-specific actions. As a result, a discussion of known and proposed mechanisms of estrogen actions in reproductive and other tissues will be presented. Building upon this information, a review of our research group's recent in vitro and in vivo studies that have focused on elucidating the mechanisms of estrogen actions in neurons of the non-sexually specialized cerebellum will be presented. While the full spectrum of estrogen action during normal cerebellar development remains unresolved, results of recent studies have revealed a pathologic role for estrogen and estrogen receptors in medulloblastoma, common pediatric brain tumors that arise from cerebellar granule cell-like precursors. The potential use of anti-estrogen signaling agents as adjuvant therapy for medulloblastoma is proposed based on those finding. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:481 / 492
页数:12
相关论文
共 97 条
[1]   G protein-coupled receptor 30 is critical for a progestin-induced growth inhibition in MCF-7 breast cancer cells [J].
Ahola, TM ;
Manninen, T ;
Alkio, N ;
Ylikomi, T .
ENDOCRINOLOGY, 2002, 143 (09) :3376-3384
[2]   Progestin upregulates G-protein-coupled receptor 30 in breast cancer cells [J].
Ahola, TM ;
Purmonen, S ;
Pennanen, P ;
Zhuang, YH ;
Tuohimaa, P ;
Ylikomi, T .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2002, 269 (10) :2485-2490
[3]   Progestin and G protein-coupled receptor 30 inhibit mitogen-activated protein kinase activity in MCF-7 breast cancer cells [J].
Ahola, TM ;
Alkio, N ;
Manninen, T ;
Ylikomi, T .
ENDOCRINOLOGY, 2002, 143 (12) :4620-4626
[4]   A novel functional estrogen receptor on human sperm membrane interferes with progesterone effects [J].
Baldi, E ;
Luconi, M ;
Muratori, M ;
Forti, G .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2000, 161 (1-2) :31-35
[5]   Differential response of estrogen receptor α and estrogen receptor β to partial estrogen agonists/antagonists [J].
Barkhem, T ;
Carlsson, B ;
Nilsson, Y ;
Enmark, E ;
Gustafsson, JÅ ;
Nilsson, S .
MOLECULAR PHARMACOLOGY, 1998, 54 (01) :105-112
[6]   Characterization of the interactions of estrogen receptor and MNAR in the activation of cSrc [J].
Barletta, F ;
Wong, CW ;
McNally, C ;
Komm, BS ;
Katzenellenbogen, B ;
Cheskis, BJ .
MOLECULAR ENDOCRINOLOGY, 2004, 18 (05) :1096-1108
[7]   Regulated expression of estrogen receptor α and β mRNA in granule cells during development of the rat cerebellum [J].
Belcher, SM .
DEVELOPMENTAL BRAIN RESEARCH, 1999, 115 (01) :57-69
[8]   Rapid estrogenic regulation of extracellular signal-regulated kinase 1/2 signaling in cerebellar granule cells involves a G protein- and protein kinase A-dependent mechanism and intracellular activation of protein phosphatase 2A [J].
Belcher, SM ;
Le, HH ;
Spurling, L ;
Wong, JK .
ENDOCRINOLOGY, 2005, 146 (12) :5397-5406
[9]  
Belcher SM, 2001, J PHARMACOL EXP THER, V299, P408
[10]   Estrogen and the developing mammalian brain [J].
Beyer, C .
ANATOMY AND EMBRYOLOGY, 1999, 199 (05) :379-390