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Cav3-Kv4 通道信号复合物对神经元活动的调节。

Regulation of neuronal activity by Cav3-Kv4 channel signaling complexes.

机构信息

Department of Physiology & Pharmacology, Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.

出版信息

Nat Neurosci. 2010 Mar;13(3):333-7. doi: 10.1038/nn.2493. Epub 2010 Feb 14.

DOI:10.1038/nn.2493
PMID:20154682
Abstract

Kv4 low voltage-activated A-type potassium channels are widely expressed in excitable cells, where they control action potential firing, dendritic activity and synaptic integration. Kv4 channels exist as a complex that includes K(+) channel-interacting proteins (KChIPs), which contain calcium-binding domains and therefore have the potential to confer calcium dependence on the Kv4 channel. We found that T-type calcium channels and Kv4 channels form a signaling complex in rat that efficiently couples calcium influx to KChIP3 to modulate Kv4 function. This interaction was critical for allowing Kv4 channels to function in the subthreshold membrane potential range to regulate neuronal firing properties. The widespread expression of these channels and accessory proteins indicates that the Cav3-Kv4 signaling complex is important for the function of a wide range of electrically excitable cells.

摘要

Kv4 低电压激活的 A 型钾通道广泛表达于可兴奋细胞,在这些细胞中,它们控制动作电位的发放、树突活动和突触整合。Kv4 通道作为一个复合物存在,包括 K(+)通道相互作用蛋白(KChIPs),其包含钙结合结构域,因此有可能赋予 Kv4 通道钙依赖性。我们发现,T 型钙通道和 Kv4 通道在大鼠中形成一个信号复合物,有效地将钙内流与 KChIP3 偶联,从而调节 Kv4 功能。这种相互作用对于允许 Kv4 通道在亚阈膜电位范围内发挥作用以调节神经元发放特性至关重要。这些通道和辅助蛋白的广泛表达表明,Cav3-Kv4 信号复合物对于广泛的电兴奋细胞的功能很重要。

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Proteomic analyses of native brain K(V)4.2 channel complexes.天然脑K(V)4.2通道复合物的蛋白质组学分析。
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Reliability of triggering postinhibitory rebound bursts in deep cerebellar neurons.触发小脑深部神经元抑制后反弹爆发的可靠性
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Rapid, bidirectional remodeling of synaptic NMDA receptor subunit composition by A-type K+ channel activity in hippocampal CA1 pyramidal neurons.
通过K4通道使A 型电流失活来控制下橄榄核中的动作电位后去极化。
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Nano-organization of synaptic calcium signaling.突触钙信号的纳米组织。
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Calcium-Dependent Regulation of Neuronal Excitability Is Rescued in Fragile X Syndrome by a Tat-Conjugated N-Terminal Fragment of FMRP.钙依赖性调节神经元兴奋性在脆性 X 综合征中通过 FMRP 的 Tat 缀合的 N 端片段得到挽救。
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Isolation and structural identification of a potassium ion channel Kv4.1 inhibitor SsTx-P2 from centipede venom.从蜈蚣毒液中分离鉴定钾离子通道 Kv4.1 抑制剂 SsTx-P2。
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2024 Apr 25;53(2):194-200. doi: 10.3724/zdxbyxb-2023-0430.
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The T-type calcium channelosome.T 型钙通道体。
Pflugers Arch. 2024 Feb;476(2):163-177. doi: 10.1007/s00424-023-02891-z. Epub 2023 Dec 1.
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