Shah M M, Mistry M, Marsh S J, Brown D A, Delmas P
Wellcome Laboratory for Molecular Pharmacology, Department of Pharmacology, University College London, Gower Street, UK.
J Physiol. 2002 Oct 1;544(Pt 1):29-37. doi: 10.1113/jphysiol.2002.028571.
M-type K(+) currents (I(K(M))) play a key role in regulating neuronal excitability. In sympathetic neurons, M-channels are thought to be composed of a heteromeric assembly of KCNQ2 and KCNQ3 K(+) channel subunits. Here, we have tried to identify the KCNQ subunits that are involved in the generation of I(K(M)) in hippocampal pyramidal neurons cultured from 5- to 7-day-old rats. RT-PCR of either CA1 or CA3 regions revealed the presence of KCNQ2, KCNQ3, KCNQ4 and KCNQ5 subunits. Single-cell PCR of dissociated hippocampal pyramidal neurons gave detectable signals for only KCNQ2, KCNQ3 and KCNQ5; where tested, most also expressed mRNA for the vesicular glutamate transporter VGLUT1. Staining for KCNQ2 and KCNQ5 protein showed punctate fluorescence on both the somata and dendrites of hippocampal neurons. Staining for KCNQ3 was diffusely distributed whereas KCNQ4 was undetectable. In perforated patch recordings, linopirdine, a specific M-channel blocker, fully inhibited I(K(M)) with an IC(50) of 3.6 +/- 1.5 microM. In 70 % of these cells, TEA fully suppressed I(K(M)) with an IC(50) of 0.7 +/- 0.1 mM. In the remaining cells, TEA maximally reduced I(K(M)) by only 59.7 +/- 5.2 % with an IC(50) of 1.4 +/- 0.3 mM; residual I(K(M)) was abolished by linopirdine. Our data suggest that KCNQ2, KCNQ3 and KCNQ5 subunits contribute to I(K(M)) in these neurons and that the variations in TEA sensitivity may reflect differential expression of KCNQ2, KCNQ3 and KCNQ5 subunits.
M型钾电流(I(K(M)))在调节神经元兴奋性中起关键作用。在交感神经元中,M通道被认为是由KCNQ2和KCNQ3钾通道亚基的异源组装体组成。在此,我们试图鉴定参与从5至7日龄大鼠培养的海马锥体神经元中I(K(M))产生的KCNQ亚基。对CA1或CA3区域进行逆转录聚合酶链反应(RT-PCR)显示存在KCNQ2、KCNQ3、KCNQ4和KCNQ5亚基。对解离的海马锥体神经元进行单细胞PCR仅得到KCNQ2、KCNQ3和KCNQ5的可检测信号;在测试的情况下,大多数神经元还表达囊泡谷氨酸转运体VGLUT1的信使核糖核酸(mRNA)。KCNQ2和KCNQ5蛋白染色显示在海马神经元的胞体和树突上有斑点状荧光。KCNQ3染色呈弥漫性分布,而KCNQ4无法检测到。在穿孔膜片钳记录中,特异性M通道阻滞剂林哌啶以3.6±1.5微摩尔/升的半数抑制浓度(IC(50))完全抑制I(K(M))。在这些细胞的70%中,四乙铵(TEA)以0.7±0.1毫摩尔/升的IC(50)完全抑制I(K(M))。在其余细胞中,TEA以1.4±0.3毫摩尔/升的IC(50)最大程度地将I(K(M))降低仅59.7±5.2%;残余的I(K(M))被林哌啶消除。我们的数据表明,KCNQ2、KCNQ3和KCNQ5亚基在这些神经元中对I(K(M))有贡献,并且TEA敏感性的差异可能反映了KCNQ2、KCNQ3和KCNQ5亚基的差异表达。