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含Kv1.4的A型钾通道在海马体兴奋性突触附近的突触前定位。

Presynaptic localization of Kv1.4-containing A-type potassium channels near excitatory synapses in the hippocampus.

作者信息

Cooper E C, Milroy A, Jan Y N, Jan L Y, Lowenstein D H

机构信息

Department of Neurology, University of California San Francisco, San Francisco, California 94143, USA.

出版信息

J Neurosci. 1998 Feb 1;18(3):965-74. doi: 10.1523/JNEUROSCI.18-03-00965.1998.

Abstract

Mammalian Shaker voltage-gated potassium channels that contain the Kv1.4 subunit exhibit rapid activation and prominent inactivation processes, which enable these channels to integrate brief (approximiately milliseconds) depolarizations over time intervals of up to tens of seconds. In the hippocampus, Kv1.4 immunoreactivity is detected at greatest density in two regions: (1) the middle molecular layer (MML), where perforant path axons synapse with dentate granule cells, and (2) the stratum lucidum (SL) of CA3, where the mossy fibers travel in tight fasciculi and form en passante synapses onto CA3 pyramidal cells. We have studied the localization of Kv1.4 within these regions in detail. First, we compared the distribution of Kv1.4 and synaptophysin (a synaptic vesicle protein primarily localized near termini) under confocal immunofluorescence microscopy. In the MML, Kv1.4 and synaptophysin immunofluorescence appeared to overlap. In the SL, however, Kv1.4 and synaptophysin staining was detected in nonoverlapping, irregular patches ( approximately 5-10 micro m in diameter). Ultrastructural studies of these two regions revealed that Kv1.4 immunoreactivity was absent from the surface membranes of cell bodies and dendrites and occurred prominently on axons, including axonal "necks" near termini. Small excitatory synaptic boutons also were labeled in the MML; by contrast, the mossy fiber synaptic expansions in the SL were not stained. These localizations may enable Kv1.4-containing channels to regulate the process of neurotransmitter release at these excitatory synapses.

摘要

含有Kv1.4亚基的哺乳动物Shaker电压门控钾通道表现出快速激活和显著的失活过程,这使得这些通道能够在长达数十秒的时间间隔内整合短暂(约几毫秒)的去极化。在海马体中,在两个区域检测到Kv1.4免疫反应性密度最高:(1)中层分子层(MML),穿通通路轴突在此与齿状颗粒细胞形成突触;(2)CA3的透明层(SL),苔藓纤维在此紧密成束走行并在CA3锥体细胞上形成旁突触。我们详细研究了Kv1.4在这些区域内的定位。首先,我们在共聚焦免疫荧光显微镜下比较了Kv1.4和突触素(一种主要定位于末端附近的突触小泡蛋白)的分布。在MML中,Kv1.4和突触素免疫荧光似乎重叠。然而,在SL中,Kv1.4和突触素染色在不重叠的不规则斑块中检测到(直径约5 - 10微米)。对这两个区域的超微结构研究表明,细胞体和树突的表面膜上没有Kv1.4免疫反应性,而在轴突上显著出现,包括靠近末端的轴突“颈部”。MML中的小兴奋性突触小体也被标记;相比之下,SL中的苔藓纤维突触膨大未被染色。这些定位可能使含有Kv1.4的通道能够调节这些兴奋性突触处的神经递质释放过程。

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