RETRACTED: Dual signaling regulated by calcyon, a D1 dopamine receptor interacting protein (Retracted Article. See vol 314, pg 1681, 2006)

被引:134
作者
Lezcano, N
Mrzljak, L
Eubanks, S
Levenson, R
Goldman-Rakic, P
Bergson, C [1 ]
机构
[1] Med Coll Georgia, Dept Pharmacol & Toxicol, Augusta, GA 30912 USA
[2] Yale Univ, Sch Med, Neurobiol Sect, New Haven, CT 06510 USA
[3] Penn State Univ, Coll Med, Dept Pharmacol, Hershey, PA 17033 USA
关键词
D O I
10.1126/science.287.5458.1660
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 synergistic response of cells to the stimulation of multiple receptors has been ascribed to receptor cross talk: however, the specific molecules that mediate the resultant signal amplification have not been defined. Here a 24-kilodalton single transmembrane protein, designated calcyon, we functionally characterize that interacts with the D1 dopamine receptor. Calcyon Localizes to dendritic spines of D1 receptor-expressing pyramidal cells in prefrontal cortex. These studies delineate a mechanism of G(q)- and G(s)-coupled heterotrimeric CTP-binding protein-coupled receptor cross talk by which D1 receptors can shift effector coupling to stimulate robust intracellular calcium (Ca(i)(2+)) release as a result of interaction with calcyon. The role of calcyon in potentiating Ca(2+)-dependent signaling should provide insight into the D1 receptor-modulated cognitive functions of prefrontal cortex.
引用
收藏
页码:1660 / 1664
页数:5
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