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CA1锥体神经元树突簇区域的通路相互作用与突触可塑性

Pathway interactions and synaptic plasticity in the dendritic tuft regions of CA1 pyramidal neurons.

作者信息

Takahashi Hiroto, Magee Jeffrey C

机构信息

Howard Hughes Medical Institute, Janelia Farm Research Campus, 19700 Helix Drive, Ashburn, VA 20147, USA.

出版信息

Neuron. 2009 Apr 16;62(1):102-11. doi: 10.1016/j.neuron.2009.03.007.


DOI:10.1016/j.neuron.2009.03.007
PMID:19376070
Abstract

Input comparison is thought to occur in many neuronal circuits, including the hippocampus, where functionally important interactions between the Schaffer collateral and perforant pathways have been hypothesized. We investigated this idea using multisite, whole-cell recordings and Ca2+ imaging and found that properly timed, repetitive stimulation of both pathways results in the generation of large plateau potentials in distal dendrites of CA1 pyramidal neurons. These dendritic plateau potentials produce widespread Ca2+ influx, large after-depolarizations, burst firing output, and long-term potentiation of perforant path synapses. Plateau duration is directly related to the strength and temporal overlap of pathway activation and involves back-propagating action potentials and both NMDA receptors and voltage-gated Ca2+ channels. Thus, the occurrence of highly correlated SC and PP input to CA1 is signaled by a dramatic change in output mode and an increase in input efficacy, all induced by a large plateau potential in the distal dendrites of CA1 pyramidal neurons.

摘要

据认为,输入比较发生在包括海马体在内的许多神经回路中,在海马体中,有人假设了谢弗侧支和穿通通路之间存在功能上重要的相互作用。我们使用多部位全细胞记录和钙离子成像来研究这一想法,发现对两条通路进行适时的重复刺激会在CA1锥体神经元的远端树突中产生大的平台电位。这些树突平台电位会产生广泛的钙离子内流、大的去极化后电位、爆发式放电输出以及穿通通路突触的长期增强。平台持续时间与通路激活的强度和时间重叠直接相关,并且涉及反向传播动作电位以及NMDA受体和电压门控钙离子通道。因此,CA1中高度相关的谢弗侧支和穿通通路输入的出现通过输出模式的显著变化和输入效能的增加来体现,所有这些都是由CA1锥体神经元远端树突中的大平台电位诱导产生的。

相似文献

[1]
Pathway interactions and synaptic plasticity in the dendritic tuft regions of CA1 pyramidal neurons.

Neuron. 2009-4-16

[2]
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[3]
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[4]
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[5]
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[6]
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J Neurophysiol. 2004-10

[7]
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[8]
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[9]
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Nature. 2002-4-18

[10]
Selective shunting of the NMDA EPSP component by the slow afterhyperpolarization in rat CA1 pyramidal neurons.

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引用本文的文献

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From Morphology to Computation: How Synaptic Organization Shapes Place Fields in CA1 Pyramidal Neurons.

bioRxiv. 2025-6-2

[2]
Dendritic inhibition terminates plateau potentials in CA1 pyramidal neurons.

bioRxiv. 2025-6-6

[3]
Alzheimer's disease patient-derived high-molecular-weight tau impairs bursting in hippocampal neurons.

Cell. 2025-7-10

[4]
Distal tuft dendrites predict properties of new hippocampal place fields.

Neuron. 2025-4-14

[5]
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Nat Neurosci. 2025-4-1

[6]
Synaptic plasticity rules driving representational shifting in the hippocampus.

Nat Neurosci. 2025-4

[7]
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[8]
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[9]
Non-apical plateau potentials and persistent firing induced by metabotropic cholinergic modulation in layer 2/3 pyramidal cells in the rat prefrontal cortex.

PLoS One. 2024-12-10

[10]
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