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树突整合的行为作用:HCN1通道限制CA1锥体神经元远端树突输入处的空间记忆和可塑性。

A behavioral role for dendritic integration: HCN1 channels constrain spatial memory and plasticity at inputs to distal dendrites of CA1 pyramidal neurons.

作者信息

Nolan Matthew F, Malleret Gaël, Dudman Josh T, Buhl Derek L, Santoro Bina, Gibbs Emma, Vronskaya Svetlana, Buzsáki György, Siegelbaum Steven A, Kandel Eric R, Morozov Alexei

机构信息

Center for Neurobiology and Behavior, Columbia University, New York, NY 10032, USA.

出版信息

Cell. 2004 Nov 24;119(5):719-32. doi: 10.1016/j.cell.2004.11.020.

Abstract

The importance of long-term synaptic plasticity as a cellular substrate for learning and memory is well established. By contrast, little is known about how learning and memory are regulated by voltage-gated ion channels that integrate synaptic information. We investigated this question using mice with general or forebrain-restricted knockout of the HCN1 gene, which we find encodes a major component of the hyperpolarization-activated inward current (Ih) and is an important determinant of dendritic integration in hippocampal CA1 pyramidal cells. Deletion of HCN1 from forebrain neurons enhances hippocampal-dependent learning and memory, augments the power of theta oscillations, and enhances long-term potentiation (LTP) at the direct perforant path input to the distal dendrites of CA1 pyramidal neurons, but has little effect on LTP at the more proximal Schaffer collateral inputs. We suggest that HCN1 channels constrain learning and memory by regulating dendritic integration of distal synaptic inputs to pyramidal cells.

摘要

长期突触可塑性作为学习和记忆的细胞基础的重要性已得到充分确立。相比之下,对于整合突触信息的电压门控离子通道如何调节学习和记忆却知之甚少。我们使用全身性或前脑限制性敲除HCN1基因的小鼠来研究这个问题,我们发现该基因编码超极化激活内向电流(Ih)的主要成分,并且是海马CA1锥体神经元树突整合的重要决定因素。从前脑神经元中删除HCN1可增强海马依赖性学习和记忆,增强θ振荡的功率,并增强CA1锥体神经元远端树突直接穿通通路输入处的长时程增强(LTP),但对更近端的Schaffer侧支输入处的LTP影响很小。我们认为,HCN1通道通过调节锥体细胞远端突触输入的树突整合来限制学习和记忆。

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