Kruse Martin, Hille Bertil
Department of Physiology and Biophysics; University of Washington; Seattle, WA USA.
Channels (Austin). 2013 Nov-Dec;7(6):530-6. doi: 10.4161/chan.25816. Epub 2013 Aug 1.
Recently, we screened several KV channels for possible dependence on plasma membrane phosphatidylinositol 4,5-bisphosphate (PI(4,5)P 2). The channels were expressed in tsA-201 cells and the PI(4,5)P 2 was depleted by several manipulations in whole-cell experiments with parallel measurements of channel activity. In contrast to reports on excised-patches using Xenopus laevis oocytes, we found only KV 7, but none of the other tested KV channels, to be strongly dependent on PI(4,5)P 2. We now have extended our study to KV 1.2 channels, a KV channel we had not previously tested, because a new published study on excised patches showed regulation of the voltage-dependence of activation by PI(4,5)P 2. In full agreement with those published results, we found a reduction of current amplitude by ~20% after depletion of PI(4,5)P 2 and a small left shift in the activation curve of KV 1.2 channels. We also found a small reduction of KV 11.1 (hERG) currents that was not accompanied by a gating shift. In conclusion, our whole-cell methods yield a PI(4,5)P 2-dependence of KV 1.2 currents in tsA-201 cells that is comparable to findings from excised patches of Xenopus laevis oocytes. We discuss possible physiological rationales for PI(4,5)P 2 sensitivity of some ion channels and insensitivity of others.
最近,我们筛选了几种钾离子通道,以确定其是否可能依赖于质膜磷脂酰肌醇-4,5-二磷酸(PI(4,5)P₂)。这些通道在tsA-201细胞中表达,在全细胞实验中通过多种操作耗尽PI(4,5)P₂,并同时测量通道活性。与使用非洲爪蟾卵母细胞进行的膜片钳实验报道不同,我们发现只有KV7通道强烈依赖于PI(4,5)P₂,而其他测试的钾离子通道均不依赖。我们现在将研究扩展到了KV1.2通道,这是我们之前未测试过的一种钾离子通道,因为一项关于膜片钳的新发表研究表明PI(4,5)P₂可调节其激活的电压依赖性。与那些已发表的结果完全一致,我们发现耗尽PI(4,5)P₂后,KV1.2通道的电流幅度降低了约20%,且激活曲线有小幅左移。我们还发现KV11.1(hERG)电流有小幅降低,但未伴随门控移位。总之,我们的全细胞方法得出tsA-201细胞中KV1.2电流对PI(4,5)P₂的依赖性与非洲爪蟾卵母细胞膜片钳实验的结果相当。我们讨论了一些离子通道对PI(4,5)P₂敏感而其他离子通道不敏感的可能生理原因。