Exchange protein activated by cAMP (Epac) mediates cAMP activation of p38 MAPK and modulation of Ca2+-dependent K+ channels in cerebellar neurons

被引:88
|
作者
Ster, Jeanne
De Bock, Frederic
Guerineau, Nathalie C.
Janossy, Andrea
Barrere-Lemaire, Stephanie
Bos, Johannes L.
Bockaert, Joel
Fagni, Laurent [1 ]
机构
[1] Univ Montpellier 1, INSERM, U661, Inst Funct Genom,CNRS,UMR 5203, F-34095 Montpellier, France
[2] Univ Montpellier 2, INSERM, U661, Inst Funct Genom,CNRS,UMR 5203, F-34095 Montpellier, France
[3] Univ Med Ctr Utrecht, Dept Physiol Chem, NL-3584 CG Utrecht, Netherlands
[4] Univ Med Ctr Utrecht, Ctr Biochem Genet, NL-3584 CG Utrecht, Netherlands
关键词
excitability; granule cells; mouse; calcium; PACAP;
D O I
10.1073/pnas.0611031104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The exchange factor directly activated by cAMP (Epac) is a newly discovered direct target for cAMP and a guanine-nucleotide exchange factor for the small GTPase Rap. Little is known about the neuronal functions of Epac. Here we show that activation of Epac by specific cAMP analogs or by the pituitary adenylate cyclase-activating polypeptide induces a potent activation of the Ca2+- sensitive big K+ channel, slight membrane hyperpolarization, and increased after-hyperpolarization in cultured cerebellar granule cells. These effects involve activation of Rap and p38 MAPK, which mobilizes intracellular Ca2+ stores. These findings reveal a cAMP Epac-dependent and protein kinase A-independent signaling cascade that controls neuronal excitability.
引用
收藏
页码:2519 / 2524
页数:6
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