Rap-linked cAMP signaling Epac proteins: Compartmentation, functioning and disease implications

被引:120
作者
Breckler, Magali [1 ,2 ,3 ]
Berthouze, Magali [1 ,2 ]
Laurent, Anne-Coline [1 ,2 ,3 ]
Crozatier, Bertrand [3 ,4 ]
Morel, Eric [3 ,4 ]
Lezoualc'h, Frank [1 ,2 ]
机构
[1] Univ Toulouse 3, UPS, F-31342 Toulouse, France
[2] INSERM, Inst Malad Metab & Cardiovasc, UMR 1048, F-31342 Toulouse, France
[3] Univ Paris 11, Paris, France
[4] INSERM, Fac Pharm, UMRS 769, F-92296 Chatenay Malabry, France
关键词
Guanine nucleotide exchange factors; cAMP; PKA; CaMKII; Phosphodiesterase; Compartmentation; G protein-coupled receptor; NUCLEOTIDE-EXCHANGE FACTOR; PANCREATIC BETA-CELLS; AIRWAY SMOOTH-MUSCLE; ENDOTHELIAL BARRIER FUNCTION; CA2+-INDUCED CA2+ RELEASE; CYCLIC-AMP ANALOG; KINASE C-EPSILON; MEDIATED ACTIVATION; BINDING PROTEINS; PHOSPHOLIPASE-C;
D O I
10.1016/j.cellsig.2011.03.007
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Epac proteins respond to the second messenger cyclic AMP (CAMP) and are activated by Gs coupled receptors. They act as specific guanine nucleotide exchange factors (GEFs) for the small G proteins, Rap1 and Rap2 of the Ras family. A plethora of studies using 8-pCPT-2'-O-Me-cAMP, an Epac agonist, has revealed the importance of these multi-domain proteins in the control of key cellular functions such as cell division, migration, growth and secretion. Epac and protein kinase A (PKA) may act independently but are often associated with the same biological process, in which they fulfill either synergistic or opposite effects. In addition, compelling evidence is now accumulating about the formation of molecular complexes in distinct cellular compartments that influence Epac signaling and cellular function. Epac is spatially and temporally regulated by scaffold protein and its effectors are interconnected with other signaling pathways. Pathophysiological changes in Epac signaling may underlie certain diseases. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1257 / 1266
页数:10
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