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[皮层肌动蛋白对上皮钠通道(ENaC)的调控机制:发动蛋白的作用]

[Mechanism of epithelial sodium channel (ENaC) regulation by cortactin: involvement of dynamin].

作者信息

Ilatovskaia D V, Pavlov T S, Neguliaev Iu A, Starushchenko A V

出版信息

Tsitologiia. 2011;53(11):903-10.

Abstract

We have recently shown that epithelial sodium channels (ENaC) are regulated by the actin-binding protein cortactin via the Arp2/3 protein complex. However, it has been also demonstrated that GTPase, dynamin, which is known to regulate clathrin-mediated endocytosis, can as well initiate signaling cascades regulated by cortactin. This study was designed to investigate the involvement of dynamin into cortactin-mediated regulation of ENaC. Initially, a recently described inhibitor of dynamin, dynasore, was used. However, use of this inhibitor seemed to be inappropriate due to discovered side effects. F. i., treatment of mpkCCD(c14) cells monolayers with dynasore (in concentrations of 10 and 100 microM) resulted in a decrease in ENaC-mediated transepithelial currents. Besides, the same concentrations of dynasore caused reduced currents in CHO cells transfected with ENaC subunits. Therefore, the data demonstrated that dynasore down regulates both native and overexpressed channel's activity and is not suitable for studies of a role of dynamin in the clathrin-mediated endocytosis of ENaC. This effect is most likely caused either by dynasore's toxic effect upon the cells or by enhanced endocytosis of ENaC-activating proteins. In the following experiments designed to study the role of dynamin different plasmids encoding mutant forms of dynamin and cortactin were used. Dominant negative dynamin K44A transfected into CHO cells together with ENaC subunits significantly increased amiloride-sensitive current density compared to cells transfected with ENaC subunits only (control); additional transfection of cortactin in this system resulted in current density restitution back to the control level. Moreover, ENaC overexpression with the SH3 domain of cortactin, which is responsible for dynamin binding, caused a decrease if ENaC current. Thus, we have shown in this study that cortactin can mediate ENaC activity not only via the Arp2/3 complex, but apart from that dynamin and related processes also might be involved into ENaC regulation by cortactin.

摘要

我们最近发现,上皮钠通道(ENaC)受肌动蛋白结合蛋白皮质肌动蛋白通过Arp2/3蛋白复合物调控。然而,也有研究表明,已知参与网格蛋白介导的内吞作用的GTP酶发动蛋白,同样可以启动由皮质肌动蛋白调控的信号级联反应。本研究旨在探究发动蛋白在皮质肌动蛋白介导的ENaC调控中的作用。最初,使用了一种最近描述的发动蛋白抑制剂——dynasore。然而,由于发现了副作用,使用这种抑制剂似乎并不合适。例如,用dynasore(浓度为10和100微摩尔)处理mpkCCD(c14)细胞单层,会导致ENaC介导的跨上皮电流降低。此外,相同浓度的dynasore会使转染了ENaC亚基的CHO细胞中的电流降低。因此,数据表明dynasore会下调天然和过表达通道的活性,不适用于研究发动蛋白在ENaC网格蛋白介导的内吞作用中的作用。这种效应很可能是由dynasore对细胞的毒性作用,或者ENaC激活蛋白的内吞作用增强所致。在接下来旨在研究发动蛋白作用的实验中,使用了编码发动蛋白和皮质肌动蛋白突变形式的不同质粒。与仅转染ENaC亚基的细胞(对照)相比,将显性负性发动蛋白K44A与ENaC亚基一起转染到CHO细胞中,显著增加了氨氯地平敏感电流密度;在该系统中额外转染皮质肌动蛋白,会使电流密度恢复到对照水平。此外,用负责与发动蛋白结合的皮质肌动蛋白的SH3结构域过表达ENaC,会导致ENaC电流降低。因此,我们在本研究中表明,皮质肌动蛋白不仅可以通过Arp2/3复合物介导ENaC活性,除此之外,发动蛋白及相关过程也可能参与皮质肌动蛋白对ENaC的调控。

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