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GABAergic interneurons targeting dendrites of pyramidal cells in the CA1 area of the hippocampus.

机译:针对海马CA1区锥体细胞树突的GABA能中间神经元。

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摘要

The dendrites of pyramidal cells are active compartments capable of independent computations, input/output transformation and synaptic plasticity. Pyramidal cells in the CA1 area of the hippocampus receive 92% of their GABAergic input onto dendrites. How does this GABAergic input participate in dendritic computations of pyramidal cells? One key to understanding their contribution to dendritic computation lies in the timing of GABAergic input in relation to excitatory transmission, back-propagating action potentials, Ca(2+) spikes and subthreshold membrane dynamics. The issue is further complicated by the fact that dendritic GABAergic inputs originate from numerous distinct sources operating with different molecular machineries and innervating different subcellular domains of pyramidal cell dendrites. The GABAergic input from distinct sources is likely to contribute differentially to dendritic computations. In this review, I describe four groups of GABAergic interneuron according to their expression of parvalbumin, cholecystokinin, axonal arborization density and long-range projections. These four interneuron groups contain at least 12 distinct cell types, which innervate mainly or exclusively the dendrites of CA1 pyramidal cells. Furthermore, I summarize the different spike timing of distinct interneuron types during gamma, theta and ripple oscillations in vivo, and I discuss some of the open questions on how GABAergic input modulates dendritic operations in CA1 pyramidal cells.
机译:锥体细胞的树突是能够独立计算,输入/输出转换和突触可塑性的活性区室。海马CA1区的金字塔形细胞接受其92%的GABA能输入到树突上。这种GABA能输入如何参与锥体细胞的树突计算?理解它们对树突计算的贡献的一个关键在于与兴奋性传递,反向传播的动作电位,Ca(2+)尖峰和亚阈值膜动力学有关的GABA能输入的时间。由于树突状的GABA能输入来自许多不同的来源,这些来源以不同的分子机制操作并支配着锥体细胞树突的不同亚细胞结构域,这一事实使问题变得更加复杂。来自不同来源的GABA能量输入可能对树突计算产生不同的贡献。在这篇综述中,我根据小白蛋白,胆囊收缩素,轴突乔化密度和远距离投射的表达描述了四组GABA能神经元。这四个中间神经元基团包含至少12种不同的细胞类型,它们主要或仅对CA1锥体细胞的树突状神经起作用。此外,我总结了体内γ,θ和波纹振荡过程中不同中间神经元类型的不同激发时间,并讨论了有关GABA能输入如何调节CA1锥体细胞中树突状操作的一些悬而未决的问题。

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