Caffrey J M, Farach M C
Department of Physiology and Molecular Biophysics, Baylor College of Medicine, Houston, Texas 77030.
Mol Pharmacol. 1988 Oct;34(4):518-26.
The nonfusing muscle cell line BC3H1 expresses functional Na and Ca channels similar to those found in skeletal muscle (1). We have utilized a monoclonal antibody that cross-reacts with a 45-50-kDa glycoprotein in differentiated BC3H1 myocytes but not in cardiac or neuronal cells. This antibody, MAb1223, specifically modulates 45Ca influx and slowly activating, dihydropyridine-sensitive Ca currents when added to BC3H1 myocytes. Low-threshold, dihydropyridine-insensitive Ca currents and Na and K currents are unaffected. MAb1223 action is voltage dependent. At very negative holding potentials, similar to those of the resting cell, MAb1223 increases slow Ca current without significant changes in the voltage dependence of activation. At more positive potentials, at which channel opening probability is reduced by inactivation, exposure to MAb1223 reduces current. Agonist and antagonist dihydropyridines modulate the action of MAb1223 on the slow Ca channel in a manner that suggests that their respective binding sites may interact directly with the channel.
不融合的肌肉细胞系BC3H1表达的功能性钠通道和钙通道与骨骼肌中的类似(1)。我们利用了一种单克隆抗体,它能与分化的BC3H1肌细胞中的一种45 - 50 kDa糖蛋白发生交叉反应,但不与心脏或神经细胞中的该糖蛋白反应。这种抗体MAb1223添加到BC3H1肌细胞中时,能特异性调节45Ca内流以及缓慢激活的、对二氢吡啶敏感的钙电流。低阈值的、对二氢吡啶不敏感的钙电流以及钠电流和钾电流不受影响。MAb1223的作用是电压依赖性的。在与静息细胞相似的非常负的钳制电位下,MAb1223增加缓慢钙电流,而激活的电压依赖性没有显著变化。在更正的电位下,此时通道开放概率因失活而降低,暴露于MAb1223会使电流减小。激动剂和拮抗剂二氢吡啶以一种表明它们各自结合位点可能直接与通道相互作用的方式调节MAb1223对缓慢钙通道的作用。