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

被引:2
|
作者
Foley, Karl [1 ,2 ]
Altimimi, Haider [3 ]
Hou, Hailong [1 ]
Zhang, Yu [1 ]
McKee, Cody [1 ,2 ]
Papasergi-Scott, Makaia M. [1 ]
Yang, Hongtian [1 ]
Mayer, Abigail [2 ]
Ward, Nancy [1 ]
MacLean, David M. [1 ]
Nairn, Angus C. [4 ]
Stellwagen, David [3 ]
Xia, Houhui [1 ,2 ]
机构
[1] Univ Rochester, Dept Pharmacol & Physiol, Med Ctr, Rochester, NY 14642 USA
[2] Univ Rochester, Sch Med & Dent, Dept Neurosci, Neurosci Grad Program,Med Ctr, Rochester, NY 14642 USA
[3] McGill Univ, Ctr Res Neurosci, Dept Neurol & Neurosurg, Montreal, PQ, Canada
[4] Yale Univ, Dept Psychiat, New Haven, CT USA
来源
基金
美国国家卫生研究院; 加拿大自然科学与工程研究理事会; 美国国家科学基金会;
关键词
protein phosphatase-1; scaffolding protein; regulatory subunit; synaptic transmission; FRET-Forster resonance energy transfer; hippocampus; inhibitor-2; CHROMOSOME SEGREGATION; PHOSPHORYLATION; ACTIN; PROTEIN-PHOSPHATASE-1; SPINOPHILIN; ISOFORMS; KINASE; SITE;
D O I
10.3389/fnsyn.2022.1021832
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 PP1 gamma, but not PP1 alpha, positively regulate synaptic transmission in hippocampal neurons. Moreover, we demonstrated that I-2 enhanced PP1 gamma interaction with its major synaptic scaffold, neurabin, by Forster 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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页数:9
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