Manhart M D, Morris R E, Bonventre P F, Leppla S, Saelinger C B
Infect Immun. 1984 Sep;45(3):596-603. doi: 10.1128/iai.45.3.596-603.1984.
Pseudomonas exotoxin A enters mouse LM fibroblasts by receptor-mediated endocytosis and ultimately causes cell death. Here we present evidence for the existence of a specific receptor for the toxin. Toxin association with LM cells at 18 and 37 degrees C, but not at 4 degrees C, was highly specific. At 37 degrees C, the association increased with time, reaching a steady state by 5 h. Binding to paraformaldehyde-fixed cells at 37 degrees C was saturable (Kd = 5.4 nM), was reversible, and indicated ca. 100,000 binding sites per cell. It is believed that receptor-bound toxin is responsible for cell death. Once the kinetics of toxin entry were described, we examined the effect of reduced temperatures on the intracellular processing of toxin and thus its expression. Toxin-induced inhibition of protein synthesis was minimal at temperatures below 20 degrees C. This was seen even though at 20 degrees C sufficient toxin was internalized to kill cells, and toxin enzyme activity was maximal. Internalization of 125I-labeled toxin, but not of 125I-labeled horseradish peroxidase (marker of fluid-phase endocytosis), became rate limiting at 20 degrees C or below. These data suggest that reduced temperatures block a step in the receptor-mediated endocytic pathway essential for the expression of Pseudomonas toxin activity.
铜绿假单胞菌外毒素A通过受体介导的内吞作用进入小鼠LM成纤维细胞,并最终导致细胞死亡。在此,我们提供了该毒素特异性受体存在的证据。毒素在18℃和37℃时与LM细胞结合,但在4℃时不结合,这种结合具有高度特异性。在37℃时,结合随时间增加,5小时后达到稳定状态。在37℃时与多聚甲醛固定细胞的结合是可饱和的(Kd = 5.4 nM),是可逆的,且表明每个细胞约有100,000个结合位点。据信,与受体结合的毒素是细胞死亡的原因。一旦描述了毒素进入的动力学,我们就研究了降低温度对毒素细胞内加工过程及其表达的影响。在低于20℃的温度下,毒素诱导的蛋白质合成抑制作用最小。即使在20℃时,有足够的毒素被内化以杀死细胞,且毒素酶活性最大,情况也是如此。在20℃或更低温度下,125I标记的毒素(而非125I标记的辣根过氧化物酶,液相内吞作用的标志物)的内化成为限速步骤。这些数据表明,降低温度会阻断受体介导的内吞途径中对铜绿假单胞菌毒素活性表达至关重要的一个步骤。