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本文引用的文献

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Ion channel gradients in the apical tuft region of CA1 pyramidal neurons.CA1 锥体神经元顶树突区域的离子通道梯度。
PLoS One. 2012;7(10):e46652. doi: 10.1371/journal.pone.0046652. Epub 2012 Oct 3.
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Intrinsic excitability of CA1 pyramidal neurones from the rat dorsal and ventral hippocampus.大鼠背侧和腹侧海马 CA1 锥体神经元的内在兴奋性。
J Physiol. 2012 Nov 15;590(22):5707-22. doi: 10.1113/jphysiol.2012.242693. Epub 2012 Sep 17.
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Differential dorso-ventral distributions of Kv4.2 and HCN proteins confer distinct integrative properties to hippocampal CA1 pyramidal cell distal dendrites.Kv4.2 和 HCN 蛋白的背腹差异分布赋予海马 CA1 锥体神经元远端树突不同的整合特性。
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Regulation of axonal HCN1 trafficking in perforant path involves expression of specific TRIP8b isoforms.调节投射路径轴突 HCN1 的转运涉及特定 TRIP8b 异构体的表达。
PLoS One. 2012;7(2):e32181. doi: 10.1371/journal.pone.0032181. Epub 2012 Feb 21.
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Signal processing in the axon initial segment.轴突起始段中的信号处理。
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Selective facilitation of LTP in the ventral hippocampus by calcium stores.钙库对腹侧海马体 LTP 的选择性促进作用。
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Grid cells use HCN1 channels for spatial scaling.网格细胞利用 HCN1 通道进行空间缩放。
Cell. 2011 Nov 23;147(5):1159-70. doi: 10.1016/j.cell.2011.08.051. Epub 2011 Nov 17.
8
Increased size and stability of CA1 and CA3 place fields in HCN1 knockout mice.HCN1 基因敲除小鼠 CA1 和 CA3 部位场的大小和稳定性增加。
Neuron. 2011 Nov 17;72(4):643-53. doi: 10.1016/j.neuron.2011.09.007.
9
Deletion of the hyperpolarization-activated cyclic nucleotide-gated channel auxiliary subunit TRIP8b impairs hippocampal Ih localization and function and promotes antidepressant behavior in mice.缺失超极化激活环核苷酸门控通道辅助亚基 TRIP8b 会损害海马 Ih 的定位和功能,并促进小鼠的抗抑郁行为。
J Neurosci. 2011 May 18;31(20):7424-40. doi: 10.1523/JNEUROSCI.0936-11.2011.
10
Errors in the measurement of voltage-activated ion channels in cell-attached patch-clamp recordings.细胞贴附式膜片钳记录中电压激活离子通道测量的误差。
Nat Commun. 2011;2:242. doi: 10.1038/ncomms1225.

HCN 亚基的差异表达改变了背侧和腹侧海马 CA1 锥体神经元中 h 通道的电压依赖性门控。

Differential expression of HCN subunits alters voltage-dependent gating of h-channels in CA1 pyramidal neurons from dorsal and ventral hippocampus.

机构信息

Center for Learning and Memory, The University of Texas at Austin, Austin, TX 78712, USA.

出版信息

J Neurophysiol. 2013 Apr;109(7):1940-53. doi: 10.1152/jn.00010.2013. Epub 2013 Jan 16.

DOI:10.1152/jn.00010.2013
PMID:23324324
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3628004/
Abstract

The rodent hippocampus can be divided into dorsal (DHC) and ventral (VHC) domains on the basis of behavioral, anatomical, and biochemical differences. Recently, we reported that CA1 pyramidal neurons from the VHC were intrinsically more excitable than DHC neurons, but the specific ionic conductances contributing to this difference were not determined. Here we investigated the hyperpolarization-activated current (I(h)) and the expression of HCN1 and HCN2 channel subunits in CA1 pyramidal neurons from the DHC and VHC. Measurement of Ih with cell-attached patches revealed a significant depolarizing shift in the V(1/2) of activation for dendritic h-channels in VHC neurons (but not DHC neurons), and ultrastructural immunolocalization of HCN1 and HCN2 channels revealed a significantly larger HCN1-to-HCN2 ratio for VHC neurons (but not DHC neurons). These observations suggest that a shift in the expression of HCN1 and HCN2 channels drives functional changes in I(h) for VHC neurons (but not DHC neurons) and could thereby significantly alter the capacity for dendritic integration of these neurons.

摘要

基于行为、解剖和生化差异,啮齿动物海马可分为背侧(DHC)和腹侧(VHC)两个区域。最近,我们报道 VHC 的 CA1 锥体神经元内在兴奋性高于 DHC 神经元,但导致这种差异的具体离子电导尚未确定。本研究旨在探讨 DHC 和 VHC 的 CA1 锥体神经元中的超极化激活电流(I(h))和 HCN1 和 HCN2 通道亚基的表达。通过细胞贴附式膜片钳记录 I(h),发现 VHC 神经元(而非 DHC 神经元)树突 h 通道的激活 V(1/2) 出现显著去极化偏移,而 HCN1 和 HCN2 通道的超微结构免疫定位显示 VHC 神经元(而非 DHC 神经元)的 HCN1 与 HCN2 通道比值显著增大。这些观察结果表明,HCN1 和 HCN2 通道表达的改变驱动了 VHC 神经元(而非 DHC 神经元)I(h)的功能变化,从而可能显著改变这些神经元的树突整合能力。