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Kv1.2 mediates heterosynaptic modulation of direct cortical synaptic inputs in CA3 pyramidal cells

机译:Kv1.2介导CA3锥体细胞中直接皮质突触输入的异突触调制。

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摘要

A short high frequency stimulation of mossy fibres (MFs) induces long-term potentiation (LTP) of direct cortical or perforant path (PP) synaptic inputs in hippocampal CA3 pyramidal cells (CA3-PCs). However, the cellular mechanism underlying this heterosynaptic modulation remains elusive. Previously, we reported that repetitive somatic firing at 10Hz downregulates Kv1.2 in the CA3-PCs. Here, we show that MF inputs induce similar somatic firing and downregulation of Kv1.2 in the CA3-PCs. The effect of Kv1.2 downregulation was specific to PP synaptic inputs that arrive at distal apical dendrites. We found that the somatodendritic expression of Kv1.2 is polarized to distal apical dendrites. Compartmental simulations based on this finding suggested that passive normalization of synaptic inputs and polarized distributions of dendritic ionic channels may facilitate the activation of dendritic Na+ channels preferentially at distal apical dendrites. Indeed, partial block of dendritic Na+ channels using 10nm tetrodotoxin brought back the enhanced PP-evoked excitatory postsynaptic potentials (PP-EPSPs) to the baseline level. These results indicate that activity-dependent downregulation of Kv1.2 in CA3-PCs mediates MF-induced heterosynaptic LTP of PP-EPSPs by facilitating activation of Na+ channels at distal apical dendrites.
机译:短时高频刺激苔藓纤维(MFs)会诱导海马CA3锥体细胞(CA3-PCs)的直接皮质或穿孔路径(PP)突触输入的长期增强(LTP)。但是,这种异突触调节基础的细胞机制仍然难以捉摸。先前,我们报道了10Hz的重复体细胞放电会下调CA3-PC中的Kv1.2。在这里,我们表明,MF输入在CA3-PC中诱导了类似的体细胞放电和Kv1.2的下调。 Kv1.2下调的作用特定于到达远端根尖树突的PP突触输入。我们发现Kv1.2的体树突状表达被极化到远端的顶端树突。基于该发现的室间模拟表明,突触输入的被动归一化和树突离子通道的极化分布可能会促进在远端根尖的树突中Na +通道的激活。的确,使用10nm河豚毒素对树突状Na +通道的部分阻滞将增强的PP诱发的兴奋性突触后电位(PP-EPSPs)恢复到基线水平。这些结果表明,CA3-PCs中Kv1.2的活性依赖性下调通过促进末梢顶端树突状细胞Na +通道的活化介导MF诱导的PP-EPSPs的突触LTP。

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