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光遗传学激酶抑制剂揭示的突触可塑性所需内源性钙/钙调蛋白依赖蛋白激酶II的动力学

Kinetics of Endogenous CaMKII Required for Synaptic Plasticity Revealed by Optogenetic Kinase Inhibitor.

作者信息

Murakoshi Hideji, Shin Myung Eun, Parra-Bueno Paula, Szatmari Erzsebet M, Shibata Akihiro C E, Yasuda Ryohei

机构信息

Supportive Center for Brain Research, National Institute for Physiological Sciences, Okazaki, Aichi 444-8585, Japan; Department of Physiological Sciences, Graduate University for Advanced Studies, Okazaki, Aichi 444-8585, Japan; Japan Science and Technology Agency (JST), Kawaguchi, Saitama 332-0012, Japan; Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.

Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA.

出版信息

Neuron. 2017 Apr 5;94(1):37-47.e5. doi: 10.1016/j.neuron.2017.02.036. Epub 2017 Mar 16.

Abstract

Elucidating temporal windows of signaling activity required for synaptic and behavioral plasticity is crucial for understanding molecular mechanisms underlying these phenomena. Here, we developed photoactivatable autocamtide inhibitory peptide 2 (paAIP2), a genetically encoded, light-inducible inhibitor of CaMKII activity. The photoactivation of paAIP2 in neurons for 1-2 min during the induction of LTP and structural LTP (sLTP) of dendritic spines inhibited these forms of plasticity in hippocampal slices of rodents. However, photoactivation ∼1 min after the induction did not affect them, suggesting that the initial 1 min of CaMKII activation is sufficient for inducing LTP and sLTP. Furthermore, the photoactivation of paAIP2 expressed in amygdalar neurons of mice during an inhibitory avoidance task revealed that CaMKII activity during, but not after, training is required for the memory formation. Thus, we demonstrated that paAIP2 is useful to elucidate the temporal window of CaMKII activation required for synaptic plasticity and learning.

摘要

阐明突触和行为可塑性所需信号活动的时间窗口对于理解这些现象背后的分子机制至关重要。在这里,我们开发了光激活自抑制钙调蛋白抑制肽2(paAIP2),这是一种基因编码的、光诱导的钙/钙调蛋白依赖性蛋白激酶II(CaMKII)活性抑制剂。在长时程增强(LTP)和树突棘的结构性LTP(sLTP)诱导过程中,将paAIP2在神经元中光激活1 - 2分钟,可抑制啮齿动物海马切片中的这些可塑性形式。然而,在诱导后约1分钟进行光激活对它们没有影响,这表明CaMKII激活的最初1分钟足以诱导LTP和sLTP。此外,在抑制性回避任务期间对小鼠杏仁核神经元中表达的paAIP2进行光激活表明,训练期间而非训练后CaMKII活性对于记忆形成是必需的。因此,我们证明了paAIP2有助于阐明突触可塑性和学习所需的CaMKII激活的时间窗口。

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