Saelinger C B, Morris R E, Foertsch G
Eur J Clin Microbiol. 1985 Apr;4(2):170-4. doi: 10.1007/BF02013592.
Experiments designed to elucidate cellular internalization of Pseudomonas aeruginosa exotoxin A are described. Inhibition of protein synthesis was used as an index of the biological activity of exotoxin A, and a biotinyl-toxin: avidin-gold system to follow its movement on the ultrastructural level. Addition of amantadine, methylamine and dansylcadaverine to cells enhanced the toxicity of exotoxin A at lower concentrations, while protecting cells at higher concentrations. In general, both sensitive and resistant cell lines responded similarly. Exposure of LM or Vero cells to an acidic extracellular pH did not overcome the protection afforded by ammonium chloride against exotoxin A cytotoxicity. This and other data suggest that sensitive and resistant cells may internalize exotoxin A in a similar manner, the toxin entering the cytosol from a prelysosomal acidic vacuole.
本文描述了旨在阐明铜绿假单胞菌外毒素A细胞内化过程的实验。蛋白质合成的抑制被用作外毒素A生物活性的指标,并且使用生物素化毒素:抗生物素蛋白-金系统在超微结构水平上追踪其移动。向细胞中添加金刚烷胺、甲胺和丹磺酰尸胺在较低浓度下增强了外毒素A的毒性,而在较高浓度下则保护细胞。总体而言,敏感和抗性细胞系的反应相似。将LM或Vero细胞暴露于酸性细胞外pH值并不能克服氯化铵对外毒素A细胞毒性的保护作用。这些及其他数据表明,敏感和抗性细胞可能以类似的方式内化外毒素A,毒素从前溶酶体酸性液泡进入细胞质溶胶。