Gadasi H, Kobiler D
Exp Parasitol. 1983 Feb;55(1):105-10. doi: 10.1016/0014-4894(83)90003-6.
Intact trophozoites of the virulent Entamoeba histolytica strain HM-1:IMSS (HM-1) destroyed a monolayer of baby hamster kidney (BHK) cells at a higher rate and efficiency than trophozoites of the nonvirulent strain HK-9. The destructive effect could be partially attributed to the proteolytic activity of the amoeba, since quantitative differences were found in the enzymatic activity of the two strains tested. Crude extracts or secreted enzymes of HM-1 trophozoites digested Azocoll, as well as the bovine cold-insoluble globulin fraction, at a much higher rate than the corresponding preparations from HK-9. This proteolytic activity was found to be activated by free sulfhydryl groups. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of the BHK cell proteins of pre- and postamoebic activities showed patterns similar to the trypsin effect on the same target cells. These enzymes were found to digest the proteins participating in the attachment of the target cells to the substrate and, consequently, cause detachment of these cells.
有毒力的溶组织内阿米巴菌株HM-1:IMSS(HM-1)的完整滋养体比无毒力菌株HK-9的滋养体以更高的速率和效率破坏了单层幼仓鼠肾(BHK)细胞。这种破坏作用可能部分归因于变形虫的蛋白水解活性,因为在所测试的两种菌株的酶活性中发现了定量差异。HM-1滋养体的粗提物或分泌酶消化偶氮胶体以及牛冷不溶性球蛋白组分的速率比HK-9的相应制剂高得多。发现这种蛋白水解活性被游离巯基激活。对阿米巴活动前后的BHK细胞蛋白质进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳,显示出与胰蛋白酶对相同靶细胞作用相似的模式。发现这些酶消化参与靶细胞与底物附着的蛋白质,从而导致这些细胞脱离。