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

被引:213
作者
Nolan, MF
Malleret, G
Dudman, JT
Buhl, DL
Santoro, B
Gibbs, E
Vronskaya, S
Buzsáki, G
Siegelbaum, SA
Kandel, ER [1 ]
Morozov, A
机构
[1] Columbia Univ, Ctr Neurobiol & Behav, New York, NY 10032 USA
[2] Rutgers State Univ, Ctr Mol & Behav Neurosci, Newark, NJ 07102 USA
[3] Columbia Univ, Dept Pharmacol, New York, NY 10032 USA
[4] Columbia Univ, Dept Physiol, New York, NY 10032 USA
[5] Columbia Univ, Dept Biochem & Biophys, New York, NY 10032 USA
[6] Columbia Univ, Dept Psychiat, New York, NY 10032 USA
[7] Columbia Univ, Howard Hughes Med Inst, New York, NY 10032 USA
[8] Columbia Univ, Kavli Inst Brain Sci, New York, NY 10032 USA
[9] NIMH, Hlth Behav Genet, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S0092-8674(04)01055-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 (I-h) 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.
引用
收藏
页码:719 / 732
页数:14
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