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用发光蛋白测量猴肾细胞内的游离钙

Measurement of intracellular free calcium in monkey kidney cells with aequorin.

作者信息

Borle A B, Snowdowne K W

出版信息

Science. 1982 Jul 16;217(4556):252-4. doi: 10.1126/science.6806904.

Abstract

A method has been developed for the measurement of intracellular free calcium in mammalian cells. The calcium-sensitive photoprotein aequorin can be incorporated into isolated cells by hypo-osmotic treatment without altering the cell viability, permeability, or metabolism. Intracellular calcium activity (Cai2+) was monitored in a perfusion system. In monkey kidney cells (LLC-MK2), Cai2+ is approximately 57 nanomoles per liter. Changes in Cai2+ with time can also be followed: exposure of the cells to anaerobiosis or the calcium ionophore A23187 reversibly increases Cai2+. The method has also been successfully tested in rat hepatocytes.

摘要

已开发出一种用于测量哺乳动物细胞内游离钙的方法。通过低渗处理可将钙敏感光蛋白水母发光蛋白导入分离的细胞中,且不会改变细胞活力、通透性或代谢。在灌注系统中监测细胞内钙活性(Cai2+)。在猴肾细胞(LLC-MK2)中,Cai2+约为每升57纳摩尔。也可追踪Cai2+随时间的变化:将细胞暴露于无氧环境或钙离子载体A23187中会使Cai2+可逆性增加。该方法也已在大鼠肝细胞中成功测试。

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