Jinno S, Jeromin A, Kosaka T
Department of Anatomy and Neurobiology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Neuroscience. 2005;134(2):483-94. doi: 10.1016/j.neuroscience.2005.04.065.
Voltage-dependent potassium (Kv) channels in the CNS are involved in regulation of subthreshold membrane potentials, and thus reception and integration of synaptic signals. Although such features are particularly important for induction of hippocampal synaptic plasticity, relatively little is known about their subcellular localization. Here we analyzed the detailed distribution of Kv4.2 potassium channels in the mouse hippocampal region using confocal and electron microscopy. At the light microscopic level, the Kv4.2 immunoreactivity occurred in a punctate fashion in the whole area of the hippocampal region. In the hippocampus proper, most of the Kv4.2-positive puncta were small, and they were abundant at the dendritic compartments of pyramidal neurons. High-resolution confocal microscopy revealed that there was no apparent association between Kv4.2-positive puncta with major synaptic markers, such as vesicular glutamate transporters and glutamic acid decarboxylase. In the subicular complex and dentate gyrus, we encountered large distinct Kv4.2-positive puncta at the perimeter of somata and proximal dendrites of principal cells. These puncta were often in contact with glutamic acid decarboxylase-positive boutons, but showed no apparent association with vesicular glutamate transporters. The glutamic acid decarboxylase-positive boutons apposing to Kv4.2-positive puncta were parvalbumin-positive. Quantitative image analysis showed that approximately half of Kv4.2-positive puncta were closely apposed to glutamic acid decarboxylase-positive boutons in the parasubiculum and dentate gyrus. Electron microscopic examination substantiated the presence of large Kv4.2-positive patches at postsynaptic sites of symmetric synapses and small patches at extrasynaptic sites. No presynaptic terminals were labeled. The present findings indicate targeted clustering of Kv4.2 potassium channels at postsynaptic sites of GABAergic synapses and extrasynaptic sites, and provide some key to understand their role in the hippocampal region.
中枢神经系统中的电压依赖性钾(Kv)通道参与阈下膜电位的调节,进而参与突触信号的接收和整合。尽管这些特征对于海马突触可塑性的诱导尤为重要,但关于它们的亚细胞定位却知之甚少。在这里,我们使用共聚焦显微镜和电子显微镜分析了Kv4.2钾通道在小鼠海马区域的详细分布。在光学显微镜水平上,Kv4.2免疫反应以点状形式出现在海马区域的整个区域。在海马体本身,大多数Kv4.2阳性斑点较小,并且在锥体神经元的树突区大量存在。高分辨率共聚焦显微镜显示,Kv4.2阳性斑点与主要突触标记物(如囊泡谷氨酸转运体和谷氨酸脱羧酶)之间没有明显关联。在海马下复合体和齿状回中,我们在主细胞的胞体周边和近端树突处遇到了大的、明显的Kv4.2阳性斑点。这些斑点经常与谷氨酸脱羧酶阳性的终扣接触,但与囊泡谷氨酸转运体没有明显关联。与Kv4.2阳性斑点相邻的谷氨酸脱羧酶阳性终扣是小白蛋白阳性的。定量图像分析表明,在副海马体和齿状回中,大约一半的Kv4.2阳性斑点与谷氨酸脱羧酶阳性终扣紧密相邻。电子显微镜检查证实,在对称突触的突触后部位存在大的Kv4.2阳性斑块,在突触外部位存在小的斑块。没有突触前终末被标记。目前的研究结果表明,Kv4.2钾通道在GABA能突触的突触后部位和突触外部位有靶向聚集,并为理解它们在海马区域的作用提供了一些关键线索。