DARPP-32: An integrator of neurotransmission

被引:530
作者
Svenningsson, P
Nishi, A
Fisone, G
Girault, JA
Nairn, AC
Greengard, P
机构
[1] Rockefeller Univ, Mol & Cellular Neurosci Lab, New York, NY 10021 USA
[2] Kurume Univ, Sch Med, Dept Physiol, Fukuoka 8300011, Japan
[3] Karolinska Inst, Dept Neurosci, F-75005 Paris, France
[4] INSERM, U536, F-75005 Paris, France
[5] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT 06508 USA
关键词
basal ganglia; striatum; protein phosphorylation; signal transduction; glutamate; dopamine; addiction;
D O I
10.1146/annurev.pharmtox.44.101802.121415
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dopamine- and cAMP-regulated phosphoprotein, Mr 32 kDa (DARPP-32), was identified initially as a major target for dopamine and protein kinase A (PKA) in striatum. However, recent advances now indicate that regulation of the state of DARPP-32 phosphorylation provides a mechanism for integrating information arriving at dopaminoceptive neurons, in multiple brain regions, via a variety of neurotransmitters, neuromodulators, neuropeptides, and steroid hormones. Activation of PKA or PKG stimulates DARPP-32 phosphorylation at Thr(34) and thereby converts DARPP-32 into a potent inhibitor of protein phosphatase-1 (PP-1). DARPP-32 is also phosphorylated at Thr(75) by Cdk5 and this converts DARPP-32 into an inhibitor of PKA. Thus, DARPP-32 has the unique property of being a dual-function protein, acting either as an inhibitor of PP-1 or of PKA. The state of phosphorylation of DARPP-32 at Thr(34) depends on the phosphorylation state of two serine residues, Ser(102) and Ser(137), which are phosphorylated by CK2 and CK1, respectively. By virtue of its ability to modulate the activity of PP-1 and PKA, DARPP-32 is critically involved in regulating electrophysiological, transcriptional, and behavioral responses to physiological and pharmacological stimuli, including antidepressants, neuroleptics, and drugs of abuse.
引用
收藏
页码:269 / 296
页数:34
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