Nakayama S, Klugbauer N, Kabeya Y, Smith L M, Hofmann F, Kuzuya M
Department of Physiology, School of Medicine, Nagoya University, Nagoya 466, Japan.
J Physiol. 2000 Jul 1;526 Pt 1(Pt 1):47-56. doi: 10.1111/j.1469-7793.2000.00047.x.
The cloned alpha 1-subunits of the smooth muscle Ca(2+) channel (alpha (1C-b)) from rabbit lung were expressed in Chinese hamster ovary cells. The effect of large depolarizations was examined using cell-attached patch clamp techniques. After large, long-duration depolarizations (to +80 mV, 4 s), the cloned smooth muscle Ca(2+) channels were still open, and also showed slow channel closure upon repolarization. The sum of unitary channel currents revealed that the tail current seen after large conditioning depolarizations had a slower deactivation time constant compared to that seen when the cell membrane was depolarized briefly with a test step (to +40 mV), suggesting that large depolarizations transform the conformation of the Ca(2+) channels to a second open state. The decay time course of the tail current induced by large conditioning depolarizations was prolonged by reducing the negativity of the repolarization step, and vice versa. Using the slow deactivating characteristic, the current-voltage relationship was directly measured by applying a ramp pulse after a large depolarization. Its slope conductance was approximately 26 pS. Since the patch pipettes contained Ca(2+) agonists, the transition of the Ca(2+) channel conformation to the second, long open state during a large depolarization was distinct from that caused by Ca(2+) agonists, suggesting that the cloned alpha 1-subunits of smooth muscle Ca(2+) channels preserve the characteristic features seen in native smooth muscle Ca(2+) channels. In addition, when skeletal muscle beta-subunits were coexpressed with the alpha 1-subunits, the long channel openings after large, long-duration depolarizations were frequently suppressed. This phenomenon could be explained if the skeletal muscle beta-subunits increased the inactivation rate during the preconditioning depolarization.
兔肺平滑肌钙通道(α(1C-b))的克隆α1亚基在中国仓鼠卵巢细胞中表达。使用细胞贴附式膜片钳技术检测大去极化的影响。在长时间的大去极化(至+80 mV,4 s)后,克隆的平滑肌钙通道仍处于开放状态,并且在复极化时也显示出缓慢的通道关闭。单位通道电流的总和显示,与用测试步骤短暂使细胞膜去极化(至+40 mV)时相比,大的预处理去极化后出现的尾电流具有更慢的失活时间常数,这表明大去极化将钙通道的构象转变为第二种开放状态。通过降低复极化步骤的负性可延长大的预处理去极化诱导的尾电流的衰减时间进程,反之亦然。利用缓慢失活特性,在大去极化后施加斜坡脉冲直接测量电流-电压关系。其斜率电导约为26 pS。由于膜片吸管中含有钙激动剂,大去极化期间钙通道构象向第二种长开放状态的转变与钙激动剂引起的转变不同,这表明平滑肌钙通道的克隆α1亚基保留了天然平滑肌钙通道中所见的特征。此外,当骨骼肌β亚基与α1亚基共表达时,长时间的大去极化后的长通道开放经常受到抑制。如果骨骼肌β亚基在预处理去极化期间增加失活速率,这种现象就可以得到解释。