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首页> 外文期刊>American Journal of Physiology >Kvl.l and Kvl.3 channels contribute to the delayed-rectifying K~+ conductance in rat choroid plexus epithelial cells
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Kvl.l and Kvl.3 channels contribute to the delayed-rectifying K~+ conductance in rat choroid plexus epithelial cells

机译:Kvl.1和Kvl.3通道有助于大鼠脉络丛上皮细胞中K +传导的延迟整流

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摘要

The choroid plexuses secrete, and maintain the composition of, the cerebrospinal fluid, K~+ channels play an important role in these processes. In this study the molecular identity and properties of the delayed-rectifying K~+ (Kv) conductance in rat choroid plexus epithelial cells were investigated. Whole cell K~+ currents were significantly reduced by 10 nM dendrotoxin-K and 1 nM margatoxin, which are specific inhibitors of Kvl.l and Kvl.3 channels, respectively. A combination of dendrotoxin-K and margatoxin caused a depolarization of the membrane potential in current-clamp experiments. Western blot analysis indicated the presence of Kvl.l and Kvl.3 proteins in the choroid plexus. Furthermore, the Kvl.3 and Kvl.l proteins appear to be expressed in the apical membrane of the epithelial cells in immunocytochemical studies.
机译:脉络丛丛分泌并维持脑脊液的组成,K +通道在这些过程中起重要作用。本研究研究了大鼠脉络丛神经上皮细胞中延迟整流K〜+(Kv)电导的分子同一性和性质。全细胞K +电流被分别为Kv1.1和Kv1.3通道的特异性抑制剂的10nM树突毒素-K和1nM玛格毒素显着降低。在电流钳实验中,树突毒素-K和玛格毒素的组合引起膜电位的去极化。 Western印迹分析表明脉络丛中存在Kv1.1和Kv1.3蛋白质。此外,在免疫细胞化学研究中,Kv1.3和Kv1.1蛋白似乎在上皮细胞的顶膜中表达。

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