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钙调蛋白依赖性激酶II调节Kv4.2通道的表达并上调神经元A型钾电流。

Calcium-calmodulin-dependent kinase II modulates Kv4.2 channel expression and upregulates neuronal A-type potassium currents.

作者信息

Varga Andrew W, Yuan Li-Lian, Anderson Anne E, Schrader Laura A, Wu Gang-Yi, Gatchel Jennifer R, Johnston Daniel, Sweatt J David

机构信息

Division of Neuroscience, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

J Neurosci. 2004 Apr 7;24(14):3643-54. doi: 10.1523/JNEUROSCI.0154-04.2004.

Abstract

Calcium-calmodulin-dependent kinase II (CaMKII) has a long history of involvement in synaptic plasticity, yet little focus has been given to potassium channels as CaMKII targets despite their importance in repolarizing EPSPs and action potentials and regulating neuronal membrane excitability. We now show that Kv4.2 acts as a substrate for CaMKII in vitro and have identified CaMKII phosphorylation sites as Ser438 and Ser459. To test whether CaMKII phosphorylation of Kv4.2 affects channel biophysics, we expressed wild-type or mutant Kv4.2 and the K(+) channel interacting protein, KChIP3, with or without a constitutively active form of CaMKII in Xenopus oocytes and measured the voltage dependence of activation and inactivation in each of these conditions. CaMKII phosphorylation had no effect on channel biophysical properties. However, we found that levels of Kv4.2 protein are increased with CaMKII phosphorylation in transfected COS cells, an effect attributable to direct channel phosphorylation based on site-directed mutagenesis studies. We also obtained corroborating physiological data showing increased surface A-type channel expression as revealed by increases in peak K(+) current amplitudes with CaMKII phosphorylation. Furthermore, endogenous A-currents in hippocampal pyramidal neurons were increased in amplitude after introduction of constitutively active CaMKII, which results in a decrease in neuronal excitability in response to current injections. Thus CaMKII can directly modulate neuronal excitability by increasing cell-surface expression of A-type K(+) channels.

摘要

钙/钙调蛋白依赖性蛋白激酶II(CaMKII)参与突触可塑性已有很长历史,但尽管钾通道在使兴奋性突触后电位(EPSP)和动作电位复极化以及调节神经元膜兴奋性方面具有重要作用,却很少有人将其作为CaMKII的靶点进行研究。我们现在发现,Kv4.2在体外是CaMKII的底物,并已确定CaMKII的磷酸化位点为Ser438和Ser459。为了测试CaMKII对Kv4.2的磷酸化是否影响通道生物物理学特性,我们在非洲爪蟾卵母细胞中表达野生型或突变型Kv4.2以及钾通道相互作用蛋白KChIP3,同时表达或不表达组成型活性形式的CaMKII,并测量每种条件下激活和失活的电压依赖性。CaMKII磷酸化对通道生物物理学特性没有影响。然而,我们发现,在转染的COS细胞中,CaMKII磷酸化会使Kv4.2蛋白水平升高,基于定点诱变研究,这种效应可归因于通道的直接磷酸化。我们还获得了确凿的生理学数据,表明CaMKII磷酸化使峰值钾电流幅度增加,从而显示出表面A型通道表达增加。此外, 引入组成型活性CaMKII后,海马锥体细胞的内源性A型电流幅度增加,这导致神经元对电流注入的兴奋性降低。因此,CaMKII可通过增加A型钾通道的细胞表面表达直接调节神经元兴奋性。

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