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首页> 外文期刊>Histochemistry and Cell Biology >Precise localization of the voltage-gated potassium channel subunits Kv3.1b and Kv3.3 revealed in the molecular layer of the rat cerebellar cortex by a pre-embedding immunogold method
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Precise localization of the voltage-gated potassium channel subunits Kv3.1b and Kv3.3 revealed in the molecular layer of the rat cerebellar cortex by a pre-embedding immunogold method

机译:通过预嵌入免疫金方法在大鼠小脑皮层的分子层中揭示了电压门控钾通道亚基Kv3.1b和Kv3.3的精确定位

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A proper motor activity relies on a correct cerebellar function. The Kv3.1 and Kv3.3 voltage-gated potassium channels are key proteins involved in cerebellar function and dysfunction, as the lack of these causes severe motor deficits. Both channel subunits are coexpressed in granule cells and are rapidly activated at relatively positive potentials to support the generation of fast action potentials. However, the contribution of each subunit to the molecular architecture of the parallel fibers, the granule cell axons, is so far unknown. The goal of this study was to elucidate the relative distribution of Kv3.1b and Kv3.3 in specific compartments of the rat parallel fibers by using a pre-embedding immunocytochemical method for electron microscopy. Numerous Kv3.1b and Kv3.3 silver-intensified gold particles were associated with membranes of parallel fiber synaptic terminals and their intervaricose segments. Kv3.1b was found in about 85% of parallel fiber synaptic terminals and in about 47% of their intervaricose portions. However, only 28% of intervaricosities and 23% of parallel fiber presynaptic boutons were Kv3.3 immunopositive. The analysis also revealed that 54% of Purkinje cell dendritic spines localized Kv3.3. Although both potassium channel subunits share localization in the same presynaptic parallel fiber compartments, the present results with the method used indicate that there are a higher percentage of parallel fibers labeled for Kv3.1b than for Kv3.3, and that the labeling intensity for each subunit is higher in specific subcompartments analyzed than in others.
机译:适当的运动活动取决于正确的小脑功能。 Kv3.1和Kv3.3电压门控钾通道是参与小脑功能和功能障碍的关键蛋白,因为缺乏这些蛋白会导致严重的运动功能障碍。两个通道亚基均在颗粒细胞中共表达,并在相对正电势下被快速激活,以支持快速动作电势的产生。然而,迄今为止还不清楚每个亚基对平行纤维的分子结构,即颗粒细胞轴突的贡献。这项研究的目的是通过使用预先嵌入的免疫细胞化学方法进行电子显微镜研究,阐明Kv3.1b和Kv3.3在大鼠平行纤维的特定区室中的相对分布。大量的Kv3.1b和Kv3.3银增强金颗粒与平行纤维突触末端的膜及其间曲段相关。在大约85%的平行纤维突触末端和大约47%的静脉曲张部分发现了Kv3.1b。但是,只有28%的间静脉曲张和23%的平行纤维突触前按钮是Kv3.3免疫阳性的。分析还显示,Purkinje细胞树突棘中有54%位于Kv3.3。尽管两个钾通道亚基在同一突触前平行纤维区室中共享定位,但使用该方法的当前结果表明,用Kv3.1b标记的平行纤维的百分比高于用Kv3.3标记的平行纤维的百分比,并且每种纤维的标记强度在所分析的特定子隔间中,该亚基要高于其他子隔间。

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