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5-羟色胺5-HT1A受体通过抑制前额叶皮层锥体神经元中的Ca2+/钙调蛋白依赖性激酶II来调节AMPA受体通道。

Serotonin 5-HT1A receptors regulate AMPA receptor channels through inhibiting Ca2+/calmodulin-dependent kinase II in prefrontal cortical pyramidal neurons.

作者信息

Cai Xiang, Gu Zhenglin, Zhong Ping, Ren Yong, Yan Zhen

机构信息

Department of Physiology and Biophysics, School of Medicine and Biomedical Sciences, State University of New York, Buffalo, New York 14214, USA.

出版信息

J Biol Chem. 2002 Sep 27;277(39):36553-62. doi: 10.1074/jbc.M203752200. Epub 2002 Jul 30.

Abstract

We have studied the regulation of AMPA (alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid) receptor channels by serotonin signaling in pyramidal neurons of prefrontal cortex (PFC). Application of serotonin reduced the amplitude of AMPA-evoked currents, an effect mimicked by 5-HT(1A) receptor agonists and blocked by 5-HT(1A) antagonists, indicating the mediation by 5-HT(1A) receptors. The serotonergic modulation of AMPA receptor currents was blocked by protein kinase A (PKA) activators and occluded by PKA inhibitors. Inhibiting the catalytic activity of protein phosphatase 1 (PP1) also eliminated the effect of serotonin on AMPA currents. Furthermore, the serotonergic modulation of AMPA currents was occluded by application of the Ca(2+)/calmodulin-dependent kinase II (CaMKII) inhibitors and blocked by intracellular injection of calmodulin or recombinant CaMKII. Application of serotonin or 5-HT(1A) agonists to PFC slices reduced CaMKII activity and the phosphorylation of AMPA receptor subunit GluR1 at the CaMKII site in a PP1-dependent manner. We concluded that serotonin, by activating 5-HT(1A) receptors, suppress glutamatergic signaling through the inhibition of CaMKII, which is achieved by the inhibition of PKA and ensuing activation of PP1. This modulation demonstrates the critical role of CaMKII in serotonergic regulation of PFC neuronal activity, which may explain the neuropsychiatric behavioral phenotypes seen in CaMKII knockout mice.

摘要

我们研究了前额叶皮质(PFC)锥体神经元中5-羟色胺信号对AMPA(α-氨基-3-羟基-5-甲基异恶唑-4-丙酸)受体通道的调节作用。应用5-羟色胺可降低AMPA诱发电流的幅度,5-HT(1A)受体激动剂可模拟该效应,5-HT(1A)拮抗剂可阻断该效应,表明其通过5-HT(1A)受体介导。蛋白激酶A(PKA)激活剂可阻断AMPA受体电流的5-羟色胺能调节作用,PKA抑制剂可使其作用消失。抑制蛋白磷酸酶1(PP1)的催化活性也可消除5-羟色胺对AMPA电流的影响。此外,应用Ca(2+)/钙调蛋白依赖性激酶II(CaMKII)抑制剂可使5-羟色胺对AMPA电流的调节作用消失,细胞内注射钙调蛋白或重组CaMKII可阻断该作用。将5-羟色胺或5-HT(1A)激动剂应用于PFC切片,可降低CaMKII活性,并以PP1依赖的方式使AMPA受体亚基GluR1在CaMKII位点的磷酸化水平降低。我们得出结论,5-羟色胺通过激活5-HT(1A)受体,抑制CaMKII,从而抑制谷氨酸能信号传递,这是通过抑制PKA并随后激活PP1实现的。这种调节作用证明了CaMKII在5-羟色胺对PFC神经元活动调节中的关键作用,这可能解释了CaMKII基因敲除小鼠中出现的神经精神行为表型。

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