Girault Jean-Antoine, Nairn Angus C
Inserm UMR-S 1270, Paris, France; Sorbonne Université, Faculty of Science and Engineering, Paris, France; Institut du Fer à Moulin, Paris, France.
Department of Psychiatry, Yale School of Medicine, Connecticut Mental Health Center, New Haven, CT, United States.
Adv Pharmacol. 2021;90:67-87. doi: 10.1016/bs.apha.2020.09.004. Epub 2020 Dec 2.
DARPP-32 (dopamine- and cAMP-regulated phosphoprotein with an apparent Mr of 32,000), now also known as phosphoprotein phosphatase 1 regulatory subunit 1B (PPP1R1B), is a potent inhibitor of protein phosphatase 1 (PP1, also known as PPP1) when phosphorylated at Thr34 by cAMP-dependent protein kinase (PKA). DARPP-32 exhibits a remarkable regional distribution in brain, roughly similar to that of dopamine innervation. Its discovery was a culmination of the long-standing effort of Paul Greengard to understand the mechanisms through which neurotransmitters such as dopamine exert their effects on target neurons. DARPP-32 is particularly enriched in striatal projection neurons where it is regulated by numerous signals through which it integrates and amplifies responses to many stimuli. Molecular studies of DARPP-32 have revealed that its regulation and function are more complex than anticipated. It is phosphorylated on multiple sites by several protein kinases that modulate DARPP-32 properties. Primarily, when phosphorylated at Thr34 DARPP-32 is a potent inhibitor of PP1, whereas when phosphorylated at Thr75 by Cdk5 it inhibits PKA. Phosphorylation at serine residues by CK1 and CK2 modulates its intracellular localization and its sensitivity to kinases or phosphatases. Modeling studies provide evidence that the signaling pathways including DARPP-32 are endowed of strong robustness and bistable properties favoring switch-like responses. Thus DARPP-32 combined with a set of other distinct signaling molecules enriched in striatal projection neurons plays a key role in the characteristic properties and physiological function of these neurons.
多巴胺和cAMP调节的磷酸化蛋白(表观分子量为32000),现也被称为蛋白磷酸酶1调节亚基1B(PPP1R1B),当被cAMP依赖性蛋白激酶(PKA)在苏氨酸34位点磷酸化时,是蛋白磷酸酶1(PP1,也称为PPP1)的强效抑制剂。DARPP - 32在大脑中呈现出显著的区域分布,大致与多巴胺神经支配的分布相似。它的发现是保罗·格林加德长期努力理解多巴胺等神经递质对靶神经元发挥作用机制的成果。DARPP - 32在纹状体投射神经元中特别富集,在那里它受到多种信号的调节,并通过这些信号整合和放大对许多刺激的反应。对DARPP - 32的分子研究表明,其调节和功能比预期的更为复杂。它在多个位点被几种蛋白激酶磷酸化,这些磷酸化调节了DARPP - 32的特性。主要是,当在苏氨酸34位点磷酸化时,DARPP - 32是PP1的强效抑制剂,而当被Cdk5在苏氨酸75位点磷酸化时,它抑制PKA。CK1和CK2在丝氨酸残基上的磷酸化调节其细胞内定位以及对激酶或磷酸酶的敏感性。建模研究提供的证据表明,包括DARPP - 32在内的信号通路具有强大的稳健性和双稳态特性,有利于开关样反应。因此,DARPP - 32与纹状体投射神经元中富集的一组其他不同的信号分子相结合,在这些神经元的特性和生理功能中起关键作用。