The G-protein-coupled CCK2 receptor associates with phospholipase Cγl

被引:13
作者
Arnould, M
Tassa, A
Ferrand, A
Archer, E
Estève, JP
Pénalba, V
Portolan, G
Escherich, A
Moroder, L
Fourmy, D
Seva, C
Dufresne, M
机构
[1] CHU Rangueil, IFR31, INSERM, U531,Inst Louis Bugnard, Toulouse, France
[2] CHU Rangueil, IFR31, Funct Proteom Facil, Toulouse, France
[3] CHU Rangueil, IFR31, Toulouse, France
[4] Max Planck Inst Biochem, Martinsried, Germany
关键词
G-protein-coupled receptor; phospholipase C; CCK2; receptor; precancerous condition; surface plasmon resonance; gastrin;
D O I
10.1016/j.febslet.2004.05.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In ElasCCK2 transgenic mice expressing cholecystokinin (CCK2) receptor in acinar cells, pancreatic phenotypic alterations and preneoplastic lesions are observed. We determined whether activation of phospholipase C gammal (PLCgamma1), known to contribute to the tumorigenesis pathophysiology, could take place as a new signaling pathway induced by the CCK2 receptor. Overexpression and activation of the PLCgamma1 in response to gastrin was observed in acinar cells. The possibility that the C-terminal tyrosine 438 of the CCK2 receptor associates with the SH2 domains of PLCgamma1 was examined. A specific interaction was demonstrated using surface plasmon resonance, confirmed in a cellular system and by molecular modeling. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:89 / 93
页数:5
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