Guan D, Tkatch T, Surmeier D J, Armstrong W E, Foehring R C
Department of Anatomy and Neurobiology, University of Tennessee, 855 Monroe Avenue, Memphis, TN 38163, USA.
J Physiol. 2007 Jun 15;581(Pt 3):941-60. doi: 10.1113/jphysiol.2007.128454. Epub 2007 Mar 22.
We determined the expression of Kv2 channel subunits in rat somatosensory and motor cortex and tested for the contributions of Kv2 subunits to slowly inactivating K+ currents in supragranular pyramidal neurons. Single cell RT-PCR showed that virtually all pyramidal cells expressed Kv2.1 mRNA and approximately 80% expressed Kv2.2 mRNA. Immunocytochemistry revealed striking differences in the distribution of Kv2.1 and Kv2.2 subunits. Kv2.1 subunits were clustered and located on somata and proximal dendrites of all pyramidal cells. Kv2.2 subunits were primarily distributed on large apical dendrites of a subset of pyramidal cells from deep layers. We used two methods for isolating currents through Kv2 channels after excluding contributions from Kv1 subunits: intracellular diffusion of Kv2.1 antibodies through the recording pipette and extracellular application of rStromatoxin-1 (ScTx). The Kv2.1 antibody specifically blocked the slowly inactivating K+ current by 25-50% (at 8 min), demonstrating that Kv2.1 subunits underlie much of this current in neocortical pyramidal neurons. ScTx (300 nM) also inhibited approximately 40% of the slowly inactivating K+ current. We observed occlusion between the actions of Kv2.1 antibody and ScTx. In addition, Kv2.1 antibody- and ScTx-sensitive currents demonstrated similar recovery from inactivation and voltage dependence and kinetics of activation and inactivation. These data indicate that both agents targeted the same channels. Considering the localization of Kv2.1 and 2.2 subunits, currents from truncated dissociated cells are probably dominated by Kv2.1 subunits. Compared with Kv2.1 currents in expression systems, the Kv2.1 current in neocortical pyramidal cells activated and inactivated at relatively negative potentials and was very sensitive to holding potential.
我们测定了大鼠体感皮层和运动皮层中Kv2通道亚基的表达,并测试了Kv2亚基对颗粒上层锥体神经元缓慢失活钾电流的作用。单细胞逆转录聚合酶链反应显示,几乎所有的锥体细胞都表达Kv2.1信使核糖核酸,约80%表达Kv2.2信使核糖核酸。免疫细胞化学揭示了Kv2.1和Kv2.2亚基分布的显著差异。Kv2.1亚基聚集并位于所有锥体细胞的胞体和近端树突上。Kv2.2亚基主要分布在深层锥体细胞亚群的大型顶端树突上。在排除Kv1亚基的作用后,我们使用两种方法分离通过Kv2通道的电流:Kv2.1抗体通过记录微管进行细胞内扩散以及细胞外应用rStromatoxin-1(ScTx)。Kv2.1抗体在8分钟时特异性地阻断了25%-50%的缓慢失活钾电流,表明Kv2.1亚基是新皮层锥体神经元中该电流的主要基础。ScTx(300 nM)也抑制了约40%的缓慢失活钾电流。我们观察到Kv2.1抗体和ScTx的作用之间存在阻断现象。此外,对Kv2.1抗体和ScTx敏感的电流在失活恢复、电压依赖性以及激活和失活动力学方面表现出相似性。这些数据表明这两种试剂作用于相同的通道。考虑到Kv2.1和2.2亚基的定位,截断的解离细胞中的电流可能主要由Kv2.1亚基主导。与表达系统中的Kv2.1电流相比,新皮层锥体细胞中的Kv2.1电流在相对负电位下激活和失活,并且对钳制电位非常敏感。