The Shaping of Two Distinct Dendritic Spikes by A-Type Voltage-Gated K+ Channels

被引:14
作者
Yang, Sungchil [1 ]
Tang, Cha-Min [2 ,3 ]
Yang, Sunggu [4 ]
机构
[1] City Univ Hong Kong, Dept Biomed Sci, Kowloon, Hong Kong, Peoples R China
[2] Univ Maryland, Sch Med, Dept Neurol, Baltimore VAMC, Bethesda, MD 20814 USA
[3] Univ Maryland, Sch Med, Dept Physiol, Baltimore VAMC, Bethesda, MD USA
[4] Incheon Natl Univ, Dept Nanobioengn, Inchon, South Korea
来源
FRONTIERS IN CELLULAR NEUROSCIENCE | 2015年 / 9卷
关键词
CA1 pyramidal neuron; voltage-gated calcium channels; A-type K+ channels; dendritic integration; dendritic excitability; DISTAL APICAL DENDRITES; FRAGILE-X; SYNAPTIC INTEGRATION; POTASSIUM CHANNELS; OBLIQUE DENDRITES; BASAL DENDRITES; POTENTIALS; EXPRESSION; PLASTICITY; KV4.2;
D O I
10.3389/fncel.2015.00469
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dendritic ion channels have been a subject of intense research in neuroscience because active ion channels in dendrites shape input signals. Ca2+-permeable channels including NMDA receptors (NMDARs) have been implicated in supralinear dendritic integration, and the I-A conductance in sublinear integration. Despite their essential roles in dendritic integration, it has remained uncertain whether these conductance coordinate with, or counteract, each other in the process of dendritic integration. To address this question, experiments were designed in hippocampal CA1 neurons with a recent 3D digital holography system that has shown excellent performance for spatial photoactivation. The results demonstrated a role of IA as a key modulator for two distinct dendritic spikes, low- and high-threshold Ca2+ spikes, through a preferential action of IA on Ca2+ permeable channel-mediated currents, over fast AMPAR-mediated currents. It is likely that the rapid kinetics of IA provides feed-forward inhibition to counteract the regenerative Ca2+ channel mediated dendritic excitability. This research reveals one dynamic ionic mechanism of dendritic integration, and may contribute to a new understanding of neuronal hyperexcitability embedded in several neural diseases such as epilepsy, fragile X syndrome and Alzheimer's disease.
引用
收藏
页码:1 / 8
页数:8
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