Activation of Mitogen-activated protein kinase (MAPK) by GnRH is cell-context dependent

被引:69
作者
Dobkin-Bekman, Masha
Naidich, Michal
Pawson, Adam J.
Millar, Robert P.
Seger, Rony
Naor, Zvi [1 ]
机构
[1] Tel Aviv Univ, George S Wise Fac Life Sci, Dept Biochem, IL-69978 Tel Aviv, Israel
[2] Queens Med Res Inst, Ctr Reprod Biol, MRC, Human Reprod Sci Unit, Edinburgh EH16 4TJ, Midlothian, Scotland
[3] Weizmann Inst Sci, Dept Regulat Biol, IL-76100 Rehovot, Israel
基金
英国医学研究理事会;
关键词
GnRH; GnRH receptor; ERK; JNK; p38; PKC; pituitary cells; prostate cancer cells;
D O I
10.1016/j.mce.2006.03.035
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
The interaction of GnRH with its cognate receptor (GnRHR) in pituitary gonadotropes includes activation of Gq/G(11) and phospholipase CP (PLC beta), which generates the second messengers inositol 1,4,5-trisphosphate (IP3) and diacylglycerol (DAG), which are required for Ca2+ mobilization and PKC isoforms activation. Activation of PKC in pituitary gonadotropes leads to the activation of the major members of the mitogen-activated protein kinase superfamily (MAPK), namely: extracellular signal-regulated kinase (ERK), jun-N-terminal Kinase (INK) and p38MAPK. The above pathways mediate GnRH-induced gonadotropin release and synthesis.,Here we summarise the diverse mechanisms utilized by GnRH to activate the MAPK members and show that they depend on "cell-context". (c) 2006 Published by Elsevier Ireland Ltd.
引用
收藏
页码:184 / 190
页数:7
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