Rosenthal J J, Vickery R G, Gilly W F
Department of Biological Sciences, Stanford University, Pacific Grove, California 93950, USA.
J Gen Physiol. 1996 Sep;108(3):207-19. doi: 10.1085/jgp.108.3.207.
We have cloned the cDNA for a squid Kvl potassium channel (SqKv1A). SqKv1A mRNA is selectively expressed in giant fiber lobe (GFL) neurons, the somata of the giant axons. Western blots detect two forms of SqKv1A in both GFL neuron and giant axon samples. Functional properties of SqKv1A currents expressed in Xenopus oocytes are very similar to macroscopic currents in GFL neurons and giant axons. Macroscopic K currents in GFL neuron cell bodies, giant axons, and in Xenopus oocytes expressing SqKv1A, activate rapidly and inactivate incompletely over a time course of several hundred ms. Oocytes injected with SqKv1A cRNA express channels of two conductance classes, estimated to be 13 and 20 pS in an internal solution containing 470 mM K. SqKv1A is thus a good candidate for the "20 pS" K channel that accounts for the majority of rapidly activating K conductance in both GFL neuron cell bodies and the giant axon.
我们已经克隆了鱿鱼Kvl钾通道(SqKv1A)的cDNA。SqKv1A mRNA在巨大纤维叶(GFL)神经元(即巨大轴突的胞体)中选择性表达。蛋白质免疫印迹法在GFL神经元和巨大轴突样本中均检测到两种形式的SqKv1A。非洲爪蟾卵母细胞中表达的SqKv1A电流的功能特性与GFL神经元和巨大轴突中的宏观电流非常相似。GFL神经元胞体、巨大轴突以及表达SqKv1A的非洲爪蟾卵母细胞中的宏观钾电流在几百毫秒的时间进程中迅速激活且不完全失活。注射了SqKv1A cRNA的卵母细胞表达两种电导类型的通道,在含有470 mM钾的内部溶液中估计分别为13和20 pS。因此,SqKv1A是“20 pS”钾通道的良好候选者,该通道在GFL神经元胞体和巨大轴突中占快速激活钾电导的大部分。