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Ion channel diversity channel expression and function in the choroid plexuses

机译:脉络丛中的离子通道多样性通道表达和功能

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摘要

Knowledge of the diversity of ion channel form and function has increased enormously over the last 25 years. The initial impetus in channel discovery came with the introduction of the patch clamp method in 1981. Functional data from patch clamp experiments have subsequently been augmented by molecular studies which have determined channel structures. Thus the introduction of patch clamp methods to study ion channel expression in the choroid plexus represents an important step forward in our knowledge understanding of the process of CSF secretion.Two K+ conductances have been identified in the choroid plexus: Kv1 channel subunits mediate outward currents at depolarising potentials; Kir 7.1 carries an inward-rectifying conductance at hyperpolarising potentials. Both K+ channels are localised at the apical membrane where they may contribute to maintenance of the membrane potential while allowing the recycling of K+ pumped in by Na+-K+ ATPase. Two anion conductances have been identified in choroid plexus. Both have significant HCO3- permeability, and may play a role in CSF secretion. One conductance exhibits inward-rectification and is regulated by cyclic AMP. The other is carried by an outward-rectifying channel, which is activated by increases in cell volume. The molecular identity of the anion channels is not known, nor is it clear whether they are expressed in the apical or basolateral membrane. Recent molecular evidence indicates that choroid plexus also expresses the non-selective cation channels such as transient receptor potential channels (TRPV4 and TRPM3) and purinoceptor type 2 (P2X) receptor operated channels. In conclusion, good progress has been made in identifying the channels expressed in the choroid plexus, but determining the precise roles of these channels in CSF secretion remains a challenge for the future.
机译:在过去的25年中,人们对离子通道形式和功能的多样性有了极大的了解。通道发现的最初动力是在1981年引入膜片钳方法。膜片钳实验的功能数据随后通过确定通道结构的分子研究得到了补充。因此,引入膜片钳方法研究脉络丛中离子通道的表达,是我们对CSF分泌过程认识的重要一步。脉络丛中已鉴定出两种K + 电导:Kv1通道亚基在去极化电位下介导向外的电流; Kir 7.1在超极化电势下具有向内整流电导。这两个K + 通道均位于顶膜,它们可能有助于维持膜电位,同时允许Na + < / sup> -K + ATPase。在脉络丛中已鉴定出两种阴离子电导。两者均具有显着的HCO3 -通透性,并且可能在CSF分泌中起作用。一种电导表现出向内整流,并受循环AMP的调节。另一个由向外整流的通道携带,该通道被细胞体积增加激活。阴离子通道的分子身份尚不清楚,也不清楚它们是否在顶膜或基底外侧膜中表达。最近的分子证据表明脉络膜丛还表达非选择性阳离子通道,例如瞬时受体电位通道(TRPV4和TRPM3)和嘌呤受体2型(P2X)受体操纵的通道。总之,在鉴定脉络丛中表达的通道方面已经取得了良好的进展,但是确定这些通道在CSF分泌中的确切作用仍然是未来的挑战。

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