Epac: Defining a New Mechanism for cAMP Action

被引:363
作者
Gloerich, Martijn [1 ]
Bos, Johannes L.
机构
[1] Univ Med Ctr, Dept Physiol Chem, Ctr Biomed Genet, NL-3584 CG Utrecht, Netherlands
关键词
G protein; guanine nucleotide exchange factor; Rap; 8-pCPT-2 '-O-Me-cAMP; cAMP-GEF; PROTEIN-KINASE-A; CA2+-INDUCED CA2+ RELEASE; ENDOTHELIAL BARRIER FUNCTION; GLUCAGON-LIKE PEPTIDE-1; PANCREATIC BETA-CELLS; EXCHANGE FACTOR EPAC2; CYCLIC-AMP; SIGNALING PATHWAY; SUBCELLULAR-LOCALIZATION; MEDIATED ACTIVATION;
D O I
10.1146/annurev.pharmtox.010909.105714
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
cAMP is a second messenger that is essential for relaying hormonal responses in many biological processes. The discovery of the cAMP target Epac explained various effects of cAMP that could not be attributed to the established targets PKA and cyclic nucleotide-gated ion channels. Epac1 and Epac2 function as guanine nucleotide exchange factors for the small G protein Rap. cAMP analogs that selectively activate Epac have helped to reveal a role for Epac in processes ranging from insulin secretion to cardiac contraction and vascular permeability Advances in the understanding of the activation mechanism of Epac and its regulation by diverse anchoring mechanisms have helped to elucidate the means by which cAMP fulfills these functions via Epac.
引用
收藏
页码:355 / 375
页数:21
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