Fink D, Contreras M L, Lelkes P I, Lazarovici P
Section on Growth Factors, National Institute of Child Health and Human Development, Bethesda, Maryland 20892.
Cell Signal. 1989;1(4):387-93. doi: 10.1016/0898-6568(89)90057-0.
Staphylococcal alpha-toxin at subcytotoxic concentrations stimulated phosphatidylinositol turnover and arachidonic acid release in undifferentiated cultures of pheochromocytoma PC12 cells. Stimulation of phospholipase A2 but not C was dependent on extracellular calcium. Addition of staphylococcal alpha-toxin to PC12 cells caused a dose-dependent, biphasic increase in intracellular calcium measured by fura-2 fluorescence technique. Elevation of intracellular Ca2+ content occurred with a time course similar to those observed for stimulation of phospholipase A2. Alteration of membrane structure and formation of staphylococcal alpha-toxin pores facilitating an influx of Ca2+, represent the probable mechanisms by which phospholipases C and A2 are activated, respectively. These results suggest a possible involvement of Ca2+, phosphoinositides and arachidonic acid metabolites in the pathogenic action of staphylococcus alpha-toxin and caution against the general usage of this toxin as a permeabilizing agent to study stimulus-secretion coupling in secretory cells.
亚细胞毒性浓度的葡萄球菌α毒素可刺激嗜铬细胞瘤PC12细胞未分化培养物中的磷脂酰肌醇周转和花生四烯酸释放。磷脂酶A2而非磷脂酶C的激活依赖于细胞外钙。将葡萄球菌α毒素添加到PC12细胞中,通过fura-2荧光技术检测到细胞内钙呈剂量依赖性双相增加。细胞内Ca2+含量的升高与磷脂酶A2激活所观察到的时间进程相似。膜结构的改变和促进Ca2+内流的葡萄球菌α毒素孔的形成,分别代表磷脂酶C和A2被激活的可能机制。这些结果表明Ca2+、磷酸肌醇和花生四烯酸代谢物可能参与葡萄球菌α毒素的致病作用,并提醒人们谨慎将这种毒素作为通透剂普遍用于研究分泌细胞中的刺激-分泌偶联。