Department of Biology, Georgia State University, 100 Piedmont Avenue, Atlanta, GA 30302-4010, USA.
J Physiol. 2012 Nov 1;590(21):5335-48. doi: 10.1113/jphysiol.2012.236885. Epub 2012 Aug 20.
The Kir4.1 channel is expressed in the brainstem, retina and kidney where it acts on K(+) transportation and pH-dependent membrane potential regulation. Its heteromerization with Kir5.1 leads to K(+) currents with distinct properties such as single-channel conductance, rectification, pH sensitivity and phosphorylation modulation. Here we show that Kir5.1 also enables S-glutathionylation to the heteromeric channel. Expressed in HEK cells, an exposure to the oxidant H(2)O(2) or diamide produced concentration-dependent inhibitions of the whole-cell Kir4.1-Kir5.1 currents. In inside-out patches, currents were inhibited strongly by a combination of diamide/GSH or H(2)O(2)/GSH but not by either alone. The currents were also suppressed by GSSG and the thiol oxidants pyridine disulfides (PDSs), suggesting S-glutathionylation. In contrast, none of the exposures had significant effects on the homomeric Kir4.1 channel. Cys158 in the TM2 helix of Kir5.1 was critical for the S-glutathionylation, which was accessible to intracellular but not extracellular oxidants. Site-directed mutagenesis of this residue (C158A or C158T) abolished the Kir4.1-Kir5.1 current modulation by oxidants, and eliminated almost completely the biochemical interaction of Kir5.1 with GSH. In tandem Kir4.1-Kir5.1 constructs, the channel with a single Cys158 was inhibited to the same degree as the wild-type channel, suggesting that one glutathione moiety is sufficient to block the channel. Consistent with the location of Cys158, GSSG inhibited the channel only when the channel was open, indicating that the channel inhibition was state dependent. The finding that the heteromeric Kir4.1-Kir5.1 channel but not the homomeric Kir4.1 is subject to the S-glutathionylation thus suggests a novel Kir4.1-Kir5.1 channel modulation mechanism that is likely to occur in oxidative stress.
Kir4.1 通道在脑干、视网膜和肾脏中表达,作用于 K(+)转运和 pH 依赖性膜电位调节。它与 Kir5.1 的异源二聚化导致具有独特特性的 K(+)电流,如单通道电导、整流、pH 敏感性和磷酸化调节。在这里,我们表明 Kir5.1 还使异源二聚体通道发生 S-谷胱甘肽化。在表达于 HEK 细胞的 Kir4.1-Kir5.1 中,暴露于氧化剂 H(2)O(2)或二酰胺会导致全细胞 Kir4.1-Kir5.1 电流产生浓度依赖性抑制。在膜片钳内面向外模式下,电流被二酰胺/GSH 或 H(2)O(2)/GSH 的组合强烈抑制,但单独使用任何一种都不会。电流也被 GSSG 和硫醇氧化剂吡啶二硫代物(PDSs)抑制,表明发生了 S-谷胱甘肽化。相比之下,这些暴露对同源 Kir4.1 通道都没有显著影响。Kir5.1 的 TM2 螺旋中的 Cys158 对 S-谷胱甘肽化至关重要,这种修饰可被细胞内但不能被细胞外氧化剂所修饰。该残基的定点突变(C158A 或 C158T)消除了氧化剂对 Kir4.1-Kir5.1 电流调节的作用,并且几乎完全消除了 Kir5.1 与 GSH 的生化相互作用。在串联 Kir4.1-Kir5.1 构建体中,具有单个 Cys158 的通道被抑制的程度与野生型通道相同,表明一个谷胱甘肽部分足以阻断通道。与 Cys158 的位置一致,只有当通道打开时 GSSG 才会抑制通道,表明通道抑制是状态依赖性的。异源二聚体 Kir4.1-Kir5.1 通道而非同源 Kir4.1 易发生 S-谷胱甘肽化的发现表明了一种新的 Kir4.1-Kir5.1 通道调节机制,这种机制可能发生在氧化应激中。