Welling A, Lacinova L, Donatin K, Ludwig A, Bosse E, Flockerzi V, Hofmann F
Institut für Pharmakologie und Toxikologie, Technische Universität München, Germany.
Pflugers Arch. 1995 Jan;429(3):400-11. doi: 10.1007/BF00374156.
The smooth muscle alpha 1Cb subunit of the L-type calcium channel was expressed alone (CHO alpha 1 cell) or together with the skeletal beta 1 (CHO alpha 1 beta 1 cell) subunit or smooth muscle beta 3 (CHO alpha 1 beta 3 cell) subunit in Chinese hamster ovary (CHO) cells. The interaction of the expressed calcium channel with the non-dihydropyridine calcium channel blocker Ro 40-5967 was studied. Ro 40-5967 decreased isradipine binding by an apparent allosteric interaction and blocked the barium inward currents (IBa) in a voltage- and use-dependent manner in all cells. The steady-state inactivation curves were shifted to hyperpolarizing potentials in the presence of Ro 40-5967. The rate of channel inactivation was increased in CHO alpha 1 and CHO alpha 1 beta 3 cells. The shift in the steady-state inactivation curve and the increase in channel inactivation were less pronounced in CHO alpha 1 beta 1 cells than in the other cell lines. Low concentrations of Ro 40-5967 increased IBa by up to 198% in 33% of the CHO alpha 1 beta 1 cells. In addition, higher concentrations of Ro 40-5967 were required to inhibit IBa in 60% of the CHO alpha 1 beta 3 cells. These results suggest that the beta subunits modify the interaction of the non-dihydropyridine Ro 40-5967 with the expressed calcium channel alpha 1 subunit.
L型钙通道的平滑肌α1Cb亚基单独在中国仓鼠卵巢(CHO)细胞中表达(CHOα1细胞),或与骨骼肌β1亚基(CHOα1β1细胞)或平滑肌β3亚基(CHOα1β3细胞)共同表达。研究了所表达的钙通道与非二氢吡啶类钙通道阻滞剂Ro 40-5967的相互作用。Ro 40-5967通过明显的变构相互作用降低了伊拉地平的结合,并以电压和使用依赖性方式阻断了所有细胞中的钡内向电流(IBa)。在Ro 40-5967存在下,稳态失活曲线向超极化电位移动。在CHOα1和CHOα1β3细胞中,通道失活速率增加。与其他细胞系相比,CHOα1β1细胞中稳态失活曲线的移动和通道失活的增加不太明显。低浓度的Ro 40-5967使33%的CHOα1β1细胞中的IBa增加高达198%。此外,60%的CHOα1β3细胞需要更高浓度的Ro 40-5967来抑制IBa。这些结果表明,β亚基改变了非二氢吡啶类Ro 40-5967与所表达的钙通道α1亚基的相互作用。