Suppr超能文献

多巴胺和腺苷酸环化酶磷酸蛋白-32:神经传递的整合因子

DARPP-32: an integrator of neurotransmission.

作者信息

Svenningsson Per, Nishi Akinori, Fisone Gilberto, Girault Jean-Antoine, Nairn Angus C, Greengard Paul

机构信息

Laboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, NY 10021, USA.

出版信息

Annu Rev Pharmacol Toxicol. 2004;44:269-96. doi: 10.1146/annurev.pharmtox.44.101802.121415.

Abstract

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 Thr34 and thereby converts DARPP-32 into a potent inhibitor of protein phosphatase-1 (PP-1). DARPP-32 is also phosphorylated at Thr75 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 Thr34 depends on the phosphorylation state of two serine residues, Ser102 and Ser137, 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.

摘要

多巴胺和环磷酸腺苷调节的磷蛋白,分子量32 kDa(DARPP - 32),最初被确定为纹状体中多巴胺和蛋白激酶A(PKA)的主要作用靶点。然而,最近的进展表明,DARPP - 32磷酸化状态的调节提供了一种机制,可整合通过多种神经递质、神经调质、神经肽和类固醇激素到达多个脑区中多巴胺感受神经元的信息。PKA或PKG的激活刺激DARPP - 32在苏氨酸34位点磷酸化,从而将DARPP - 32转化为蛋白磷酸酶 - 1(PP - 1)的强效抑制剂。DARPP - 32也可被细胞周期蛋白依赖性激酶5(Cdk5)在苏氨酸75位点磷酸化,这使DARPP - 32转化为PKA的抑制剂。因此,DARPP - 32具有作为双功能蛋白的独特性质,既可以作为PP - 1的抑制剂,也可以作为PKA的抑制剂。DARPP - 32在苏氨酸34位点的磷酸化状态取决于两个丝氨酸残基,即丝氨酸102和丝氨酸137的磷酸化状态,它们分别被酪蛋白激酶2(CK2)和酪蛋白激酶1(CK1)磷酸化。凭借其调节PP - 1和PKA活性的能力,DARPP - 32在调节对生理和药理刺激(包括抗抑郁药、抗精神病药和滥用药物)的电生理、转录和行为反应中起关键作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验