Lutz F, Maurer M, Failing K
Toxicon. 1987;25(3):293-305. doi: 10.1016/0041-0101(87)90258-3.
Increased plasma membrane permeability induced by a purified cytotoxic protein from Pseudomonas aeruginosa was studied using mouse Ehrlich ascites tumor cells in incubation medium containing an osmotic stabilizer. In the presence of serum albumin, 40 nM of the cytotoxin was required for cationic imbalance of 2.7 X 10(7) cells per ml at pH 7.4. The rate of passive flux of water-soluble markers with a molecular radius range between 0.3 and 4 nm was used to calculate the size of functional transmembrane pores. Within a short time of intoxication pores of 1 nm in radius were formed. Their stability is inferred from the constant rate of leakage of the most restricted marker during intoxication (60-90 min). The cytotoxin-induced plasma membrane damage led to loss of essential low molecular weight substances and was associated with a decrease of tumor propagation rate in mice. Regression analysis of these functional parameters indicate the reversibility of plasma membrane disorganization up to complete breakdown of the Na+/K+ gradient. The cell can even tolerate partial loss of larger cytosolic compounds under conditions of limited intoxication.
使用含有渗透稳定剂的培养介质中的小鼠艾氏腹水肿瘤细胞,研究了铜绿假单胞菌纯化的细胞毒性蛋白诱导的质膜通透性增加。在血清白蛋白存在的情况下,在pH 7.4时,每毫升2.7×10⁷个细胞的阳离子失衡需要40 nM的细胞毒素。使用分子半径在0.3至4 nm之间的水溶性标记物的被动通量速率来计算功能性跨膜孔的大小。在中毒后的短时间内形成了半径为1 nm的孔。它们的稳定性是从中毒期间(60 - 90分钟)最受限标记物的恒定泄漏率推断出来的。细胞毒素诱导的质膜损伤导致必需的低分子量物质流失,并与小鼠肿瘤增殖速率的降低有关。对这些功能参数的回归分析表明,直到Na⁺/K⁺梯度完全破坏,质膜紊乱都是可逆的。在有限中毒的条件下,细胞甚至可以耐受较大胞质化合物的部分损失。