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Regulation of sodium channel activity by capping of actin filaments

机译:通过封闭肌动蛋白丝调节钠通道活性

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Ion transport in various tissues can be regulated by the cortical actin cytoskeleton. Specifically, involvement of actin dynamics in the regulation of nonvoltage-gated sodium channels has been shown. Herein, inside-out patch clamp experiments were performed to study the effect of the heterodimeric actin capping protein CapZ on sodium channel regulation in leukemia K562 cells. The channels were activated by cytochalasin-induced disruption of actin filaments and inactivated by G-actin under ionic conditions promoting rapid actin polymerization. CapZ had no direct effect on channel activity. However, being added together with G-actin, CapZ prevented actin-induced channel inactivation, and this effect occurred at CapZ/actin molar ratios from 1:5 to 1:100. When actin was allowed to polymerize at the plasma membrane to induce partial channel inactivation, subsequent addition of CapZ restored the channel activity. These results can be explained by CapZ-induced inhibition of further assembly of actin filaments at the plasma membrane due to the modification of actin dynamics by CapZ. No effect on the channel activity was observed in response to F-actin, confirming that the mechanism of channel inactivation does not involve interaction of the channel with preformed filaments. Our data show that actin-capping protein can participate in the cytoskeleton-associated regulation of sodium transport in nonexcitable cells. [References: 45]
机译:皮质肌动蛋白细胞骨架可调节各种组织中的离子运输。具体而言,已显示肌动蛋白动力学参与非电压门控钠通道的调节。在这里,进行了由内而外的膜片钳实验,以研究异二聚肌动蛋白封端蛋白CapZ对白血病K562细胞钠通道调节的影响。在细胞松弛素诱导的肌动蛋白丝破坏中激活了通道,在离子条件下由G-肌动蛋白激活了通道,从而促进了肌动蛋白的快速聚合。 CapZ对渠道活动没有直接影响。但是,CapZ与G-肌动蛋白一起添加可防止肌动蛋白诱导的通道失活,并且这种作用发生在CapZ /肌动蛋白摩尔比为1:5至1:100的情况下。当肌动蛋白在质膜上聚合以诱导部分通道失活时,随后添加CapZ可恢复通道活性。这些结果可以通过CapZ诱导的肌动蛋白丝在质膜上进一步组装的抑制来解释,这是由于CapZ对肌动蛋白动力学的影响。没有观察到响应F-肌动蛋白对通道活性的影响,证实了通道失活的机制不涉及通道与预成型丝的相互作用。我们的数据表明,肌动蛋白封端蛋白可以参与非兴奋性细胞中钠转运的细胞骨架相关调节。 [参考:45]

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