Group I metabotropic glutamate receptor-mediated gene expression in striatal neurons

被引:27
|
作者
Mao, Li-Min [1 ]
Zhang, Guo-Chi [1 ]
Liu, Xian-Yu [1 ]
Fibuch, Eugene E. [2 ]
Wang, John Q. [1 ,2 ,3 ]
机构
[1] Univ Missouri, Sch Med, Dept Basic Med Sci, Kansas City, MO 64108 USA
[2] Univ Missouri, Sch Med, Dept Anesthesiol, Kansas City, MO 64108 USA
[3] Univ Missouri, Sch Pharm, Dept Pharmacol, Kansas City, MO 64108 USA
关键词
dopamine; nucleus accumbens; CREB; MAPK; ERK; homer; fos; dynorphin;
D O I
10.1007/s11064-008-9654-4
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
Group I mGluRs (mGluR1/5) are G-protein-coupled receptors and are abundantly expressed in most of medium spiny projection neurons in the striatum. Recent evidence demonstrates that group I mGluRs are among essential regulators for constitutive and inducible gene expression in host neurons. Upon activation, mGluR1/5 signals activate extracellular signal-regulated kinases (ERKs) which in turn phosphorylate transcription factors such as cAMP response element-binding protein (CREB) and Elk-1, and thereby facilitate immediate early gene and opioid peptide gene expression. The conventional mGluR1/5 signaling cascade (phosphoinositide hydrolysis and intracellular Ca(2+) release) participates in linking mGluR1/5 to ERK. Additionally, the prominent mGluR1/5 adaptor protein Homer contributes to assemble an efficient signaling apparatus connecting mGluR1/5 to gene expression. The mGluR1/5 linkage to transcription also functions in dopamine-stimulated gene expression. Together, the mGluR1/5-mediated gene expression constitutes a transcription-dependent mechanism underlying molecular adaptations and plasticity related to the pathogenesis of various mental illnesses.
引用
收藏
页码:1920 / 1924
页数:5
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