Chapman H, Piggot C, Andrews P W, Wann K T
Welsh School of Pharmacy, Cardiff University, King Edward VII Avenue, Cardiff CF10 3XF, UK.
Brain Res. 2007 Jan 19;1129(1):15-25. doi: 10.1016/j.brainres.2006.10.060. Epub 2006 Dec 6.
Large-conductance calcium-activated potassium (BK(Ca)) channels were studied in inside-out patches of human NTERA2 neuronal cells (NT2-N). In symmetrical (140 mM) K(+) the channel mean conductance was 265 pS, the current reversing at approximately 0 mV. It was selective (P(K)/P(Na)=20:1) and blocked by internal paxilline and TEA. The open probability-voltage relationship for BK(Ca) was fitted with a Boltzmann function, the V((1/2)) being 76.3 mV, 33.6 mV and -14.1 mV at 0.1 muM, 3.3 muM and 10 muM Ca(2+), respectively. The relationship between open probability and Ca(2+) was fitted by the Hill equation (Hill coefficient 2.7, half maximal activation at 2.0 muM Ca(2+)). Open and closed dwell time histograms were fitted by the sum of two and three voltage-dependent exponentials, respectively. Increasing Ca(2+) produced both an increase in the longer open time constant and a decrease in the longest closed time constant, so increasing mean open time. "Intracellular" ATP evoked a concentration-dependent increase in NT2-N BK(Ca) activity. At +40 mV half-maximum activation occurred at an ATP of 3 mM (30 nM Ca(2+)). ADP and GTP were less potent, and AMP-PNP was inactive. This is the first characterisation of a potassium channel in NT2-N cells showing that it is similar to the BK(Ca) channel of other preparations.
在人NTERA2神经元细胞(NT2-N)的内向外膜片上研究了大电导钙激活钾(BK(Ca))通道。在对称(140 mM)钾离子溶液中,通道的平均电导为265 pS,电流在约0 mV处反转。该通道具有选择性(钾离子与钠离子的通透率之比为20:1),并被胞内的紫杉醇和四乙铵阻断。BK(Ca)通道的开放概率-电压关系用玻尔兹曼函数拟合,在胞内钙离子浓度为0.1 μM、3.3 μM和10 μM时,半激活电压分别为76.3 mV、33.6 mV和 -14.1 mV。开放概率与胞内钙离子浓度的关系用希尔方程拟合(希尔系数为2.7,在胞内钙离子浓度为2.0 μM时达到半最大激活)。开放和关闭驻留时间直方图分别用两个和三个电压依赖性指数之和拟合。增加胞内钙离子浓度会使较长的开放时间常数增加,最长的关闭时间常数减小,从而增加平均开放时间。“胞内”ATP引起NT2-N细胞中BK(Ca)通道活性呈浓度依赖性增加。在 +40 mV时,半最大激活发生在胞内ATP浓度为3 mM(胞内钙离子浓度为30 nM)时。ADP和GTP的作用较弱,而AMP-PNP无活性。这是首次对NT2-N细胞中的钾通道进行表征,表明它与其他制剂中的BK(Ca)通道相似。