Dekker John P, Yellen Gary
Department of Neurobiology Harvard Medical School, Boston, MA 02115, USA.
J Gen Physiol. 2006 Nov;128(5):561-7. doi: 10.1085/jgp.200609599. Epub 2006 Oct 16.
HCN pacemaker channels (I(f), I(q), or I(h)) play a fundamental role in the physiology of many excitable cell types, including cardiac myocytes and central neurons. While cloned HCN channels have been studied extensively in macroscopic patch clamp experiments, their extremely small conductance has precluded single channel analysis to date. Nevertheless, there remain fundamental questions about HCN gating that can be resolved only at the single channel level. Here we present the first detailed single channel study of cloned mammalian HCN2. Excised patch clamp recordings revealed discrete hyperpolarization-activated, cAMP-sensitive channel openings with amplitudes of 150-230 fA in the activation voltage range. The average conductance of these openings was approximately 1.5 pS at -120 mV in symmetrical 160 mM K(+). Some traces with multiple channels showed unusual gating behavior, characterized by a variable long delay after a voltage step followed by runs of openings. Noise analysis on macroscopic currents revealed fluctuations whose magnitudes were systematically larger than predicted from the actual single channel current size, consistent with cooperativity between single HCN channels.
超极化激活的环核苷酸门控(HCN)起搏通道(I(f)、I(q)或I(h))在包括心肌细胞和中枢神经元在内的多种可兴奋细胞类型的生理学中发挥着重要作用。虽然克隆的HCN通道已在宏观膜片钳实验中得到广泛研究,但由于其电导极小,迄今为止尚未进行单通道分析。然而,关于HCN门控仍存在一些基本问题,这些问题只有在单通道水平上才能得到解决。在此,我们首次对克隆的哺乳动物HCN2进行了详细的单通道研究。膜片钳记录显示,在激活电压范围内,出现了离散的超极化激活、对cAMP敏感的通道开放,其幅度为150 - 230飞安。在对称的160 mM K(+)中,-120 mV时这些开放的平均电导约为1.5皮西门子。一些具有多个通道的记录显示出异常的门控行为,其特征是电压阶跃后有可变的长延迟,随后是一连串的开放。对宏观电流的噪声分析揭示了波动,其幅度系统地大于根据实际单通道电流大小预测的值,这与单个HCN通道之间的协同作用一致。