The dopamine D4 receptor activates intracellular platelet-derived growth factor receptor β to stimulate ERK1/2

被引:12
|
作者
Gill, Robin S. [1 ]
Hsiung, Marilyn S. [1 ,3 ]
Sum, Chi S. [1 ]
Lavine, Natalie [1 ,3 ]
Clark, Stewart D. [1 ]
Van Tol, Hubert H. M. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Ctr Addict & Mental Hlth, Mol Neurobiol Lab, Toronto, ON M5T 1R8, Canada
[2] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[3] Univ Toronto, Dept Pharmacol, Toronto, ON, Canada
[4] Univ Toronto, Dept Physiol, Toronto, ON, Canada
[5] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A1, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
Dopamine; Platelet-derived growth factor; Transactivation; G protein-coupled receptor; PROTEIN-KINASE-C; TYROSINE KINASE; TRANSACTIVATION; DEGRADATION; PDGF; D-4; MEDIATE; SURFACE;
D O I
10.1016/j.cellsig.2009.09.031
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dopamine receptors are GPCRs that play important roles in locomotion, reward, and cognitive processes. Previously, we demonstrated that this receptor transactivates PDGFR beta to modulate ERK1/2 and NMDA receptor activity. Downregulation of maturely glycosylated PDGFR beta by prolonged exposure to PDGF-BB eliminated PDGF-BB-mediated ERK1/2 activation. The DRD4-mediated ERK1/2 response was only partially blunted by PDGF-BB-mediated downregulation, but remained sensitive to the PDGFW kinase inhibitor tyrphostin A9. Tunicamycin prevented the N-linked glycosylation and maturation of PDGFR beta as well as its activation by PDGF-BB. However, upon tunicamycin treatment, DRD4 continued to signal to ERK1/2 in a tyrphostin A9-sensitive manner. Collectively, our observations indicate that DRD4, unlike PDGF-BB, can activate a pool of intracellularly located PDGFR beta. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:285 / 290
页数:6
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