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A family of hyperpolarization-activated mammalian cation channels.

机译:一类超极化激活的哺乳动物阳离子通道。

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摘要

Pacemaker activity of spontaneously active neurons and heart cells is controlled by a depolarizing, mixed Na+/K+ current, named Ih (or I(f) in the sinoatrial node of the heart). This current is activated on hyperpolarization of the plasma membrane. In addition to depolarizing pacemaker cells, Ih is involved in determining the resting membrane potential of neurons and provides a mechanism to limit hyperpolarizing currents in these cells. Hormones and neurotransmitters that induce a rise in cyclic AMP levels increase Ih by a mechanism that is independent of protein phosphorylation, and which involves direct binding of the cyclic nucleotide to the channel that mediates Ih. Here we report the molecular cloning and functional expression of the gene encoding a hyperpolarization-activated cation channel (HAC1) that is present in brain and heart. This channel exhibits the general properties of Ih channels. We have also identified full-length sequences of two related channels, HAC2 and HAC3, that are specifically expressed in the brain, indicating the existence of a family of hyperpolarization-activated cation channels.
机译:自发活跃的神经元和心脏细胞的起搏器活动由去极化的混合Na + / K +电流控制,该电流称为Ih(或心脏窦房结中的I(f))。该电流在质膜超极化时被激活。除了使起搏器细胞去极化外,Ih还参与确定神经元的静息膜电位,并提供一种限制这些细胞中超极化电流的机制。诱导环状AMP水平升高的激素和神经递质通过一种独立于蛋白质磷酸化的机制增加Ih,该机制涉及环状核苷酸与介导Ih的通道的直接结合。在这里,我们报告编码存在于脑和心脏中的超极化激活阳离子通道(HAC1)的基因的分子克隆和功能表达。此通道具有Ih通道的一般属性。我们还确定了两个相关通道,HAC2和HAC3的全长序列,它们在大脑中特异性表达,表明存在超极化激活阳离子通道家族。

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