Hart P J, Overturf K E, Russell S N, Carl A, Hume J R, Sanders K M, Horowitz B
Department of Physiology, University of Nevada School of Medicine, Reno 89557.
Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9659-63. doi: 10.1073/pnas.90.20.9659.
A cDNA (CSMK1) encoding a delayed rectifier K+ channel of the Kv1.2 class was cloned from canine colonic circular smooth muscle and expressed in Xenopus oocytes. These channels appear to be uniquely expressed in gastrointestinal muscles and may participate in the electrical slow wave activity. Functional expression of CSMK1 in Xenopus oocytes demonstrated a K+ current that activated in a voltage-dependent manner upon depolarization. This current was highly sensitive to 4-aminopyridine (IC50, 74 microM). A low-conductance K+ channel was identified in inside-out patches from oocytes injected with CSMK1. This channel displayed a linear current-voltage relation with a slope conductance of 14 pS. The channels were blocked in a concentration-dependent manner by 4-aminopyridine. Northern blot analysis demonstrated that CSMK1 is expressed in a wide variety of gastrointestinal smooth muscles. Portal vein, renal artery, and uterus do not express CSMK1, suggesting that, among smooth muscles, expression of this K+ channel may be restricted to gastrointestinal smooth muscles. CSMK1 is 91% homologous to RAK, a delayed rectifier K+ channel cloned from rat heart, but displays unique pharmacological properties and tissue distribution.
从犬结肠环形平滑肌中克隆出一个编码Kv1.2类延迟整流钾通道的cDNA(CSMK1),并在非洲爪蟾卵母细胞中表达。这些通道似乎在胃肠肌肉中独特表达,可能参与电慢波活动。CSMK1在非洲爪蟾卵母细胞中的功能性表达显示出一种钾电流,该电流在去极化时以电压依赖方式激活。该电流对4-氨基吡啶高度敏感(IC50,74微摩尔)。在注射了CSMK1的卵母细胞的内面向外膜片中鉴定出一种低电导钾通道。该通道呈现线性电流-电压关系,斜率电导为14皮安。这些通道被4-氨基吡啶以浓度依赖方式阻断。Northern印迹分析表明CSMK1在多种胃肠平滑肌中表达。门静脉、肾动脉和子宫不表达CSMK1,这表明在平滑肌中,这种钾通道的表达可能仅限于胃肠平滑肌。CSMK1与从大鼠心脏克隆的延迟整流钾通道RAK有91%的同源性,但具有独特的药理学特性和组织分布。