蛋白磷酸酶-1抑制剂-2促进PP1γ正调控突触传递。

IF 2.8 4区 医学 Q2 NEUROSCIENCES
Karl Foley, Haider Altimimi, Hailong Hou, Yu Zhang, Cody McKee, Makaía M Papasergi-Scott, Hongtian Yang, Abigail Mayer, Nancy Ward, David M MacLean, Angus C Nairn, David Stellwagen, Houhui Xia
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引用次数: 0

摘要

抑制剂-2 (I-2)是蛋白磷酸酶-1 (PP1)的原型抑制剂,PP1是一种主要的丝氨酸-苏氨酸磷酸酶,调节突触可塑性和学习记忆。虽然I-2在体外是PP1的有效抑制剂,但我们之前的工作已经阐明,在体内,I-2可能作为PP1的正调节因子。在这里,我们发现I-2和PP1γ,而不是PP1α,正向调节海马神经元的突触传递。此外,我们通过Förster共振能量转移(FRET)/荧光寿命成像显微镜(FLIM)研究证明,I-2增强了PP1γ与其主要突触支架neurabin的相互作用,而对PP1自身抑制性磷酸化的影响有限。此外,我们的研究表明,体内I-2对PP1活性的影响是由I-2苏氨酸-72磷酸化决定的。因此,我们的工作证明了I-2在突触传递中积极调节PP1功能的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Protein phosphatase-1 inhibitor-2 promotes PP1<i>γ</i> positive regulation of synaptic transmission.

Protein phosphatase-1 inhibitor-2 promotes PP1<i>γ</i> positive regulation of synaptic transmission.

Protein phosphatase-1 inhibitor-2 promotes PP1<i>γ</i> positive regulation of synaptic transmission.

Protein phosphatase-1 inhibitor-2 promotes PP1γ positive regulation of synaptic transmission.

Inhibitor-2 (I-2) is a prototypic inhibitor of protein phosphatase-1 (PP1), a major serine-threonine phosphatase that regulates synaptic plasticity and learning and memory. Although I-2 is a potent inhibitor of PP1 in vitro, our previous work has elucidated that, in vivo, I-2 may act as a positive regulator of PP1. Here we show that I-2 and PP1γ, but not PP1α, positively regulate synaptic transmission in hippocampal neurons. Moreover, we demonstrated that I-2 enhanced PP1γ interaction with its major synaptic scaffold, neurabin, by Förster resonance energy transfer (FRET)/Fluorescence lifetime imaging microscopy (FLIM) studies, while having a limited effect on PP1 auto-inhibitory phosphorylation. Furthermore, our study indicates that the effect of I-2 on PP1 activity in vivo is dictated by I-2 threonine-72 phosphorylation. Our work thus demonstrates a molecular mechanism by which I-2 positively regulates PP1 function in synaptic transmission.

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来源期刊
CiteScore
7.10
自引率
2.70%
发文量
74
审稿时长
14 weeks
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