Thor H, Hartzell P, Orrenius S
J Biol Chem. 1984 May 25;259(10):6612-5.
Incubation of freshly isolated rat hepatocytes with exogenous ATP, but not with succinate, resulted in intracellular Ca2+ accumulation which was partly prevented when the inhibitor of mitochondrial Ca2+ sequestration, ruthenium red, was also present in the medium. Although the bulk of the accumulated Ca2+ was sequestered by the mitochondria, formation of surface blebs and stimulation of phosphorylase alpha activity during incubation of the hepatocytes with ATP indicate that this treatment was also associated with an increase in cytosolic free Ca2+ concentration. When hepatocytes loaded with Ca2+ by preincubation with ATP were exposed to either 2-methyl-1,4-naphthoquinone or t-butyl hydroperoxide, the cytotoxicity of both agents was markedly potentiated. Our results suggest that ATP-induced Ca2+ accumulation in hepatocytes is not due to contamination of the cell suspension with damaged cells or free intracellular organelles and that the intracellular Ca2+ concentration can affect the response to toxic agents.
用外源性ATP而非琥珀酸孵育新鲜分离的大鼠肝细胞,会导致细胞内Ca2+积累。当线粒体Ca2+隔离抑制剂钌红也存在于培养基中时,这种积累会部分受到抑制。尽管大部分积累的Ca2+被线粒体隔离,但在肝细胞与ATP孵育期间,表面泡的形成和磷酸化酶α活性的刺激表明,这种处理也与胞质游离Ca2+浓度的增加有关。当通过与ATP预孵育而加载Ca2+的肝细胞暴露于2-甲基-1,4-萘醌或叔丁基过氧化氢时,这两种试剂的细胞毒性均明显增强。我们的结果表明,ATP诱导的肝细胞内Ca2+积累并非由于细胞悬液被受损细胞或游离细胞内细胞器污染所致,并且细胞内Ca2+浓度可影响对有毒试剂的反应。