Rusch N J, Hermsmeyer K
Department of Physiology, Medical College of Wisconsin, Milwaukee 53226.
Mol Cell Biochem. 1988 Mar-Apr;80(1-2):87-93. doi: 10.1007/BF00231007.
The direct measurement of transmembrane calcium current in single vascular muscle cells has been accomplished recently using the whole-cell voltage-clamp technique. The small size of the vascular muscle cell and the proportionately smaller magnitude of its inward calcium current necessitate refined instrumentation, but also make the vascular muscle cell an ideal candidate for whole-cell voltage-clamp recording. Calcium current in vascular muscle cells appears to have some, but not all, characteristics in common with calcium currents similarly isolated in neuronal and cardiac cells, including voltage-dependent activation and steady-state inactivation of calcium current, the presence of two current types, and sensitivity to inorganic and organic calcium channel modulating drugs. Future voltage-clamp analysis of calcium currents in vascular muscle is needed to further our understanding of the control of the calcium channels in physiological and pathophysiological states.
最近,采用全细胞电压钳技术实现了对单个血管肌细胞跨膜钙电流的直接测量。血管肌细胞体积小,其内向钙电流幅度相对较小,这不仅需要精密的仪器,也使血管肌细胞成为全细胞电压钳记录的理想对象。血管肌细胞中的钙电流似乎具有一些(但并非全部)与在神经元和心肌细胞中类似分离出来的钙电流相同的特性,包括钙电流的电压依赖性激活和稳态失活、两种电流类型的存在以及对无机和有机钙通道调节药物的敏感性。未来需要对血管肌细胞中的钙电流进行电压钳分析,以进一步了解生理和病理生理状态下钙通道的调控机制。