Kutner S, Breuer W V, Ginsburg H, Aley S B, Cabantchik Z I
J Cell Physiol. 1985 Dec;125(3):521-7. doi: 10.1002/jcp.1041250323.
Human intraerythrocytic malarial parasites (Plasmodium falciparum) induce permeability changes in the membrane of their host cells. The differential permeability of infected erythrocytes at various stages of parasite growth, in combination with density gradient centrifugation, was used to fractionate parasitized cells according to their developmental stage. By this method it was possible to obtain cell fractions consisting essentially of erythrocytes infected with the youngest parasite stage (i.e., rings). These preparations were used for the measurement of transport of various solutes. It is shown that permeabilization of host erythrocyte membrane appears as early as 6 h after parasite invasion of the erythrocyte and increases gradually with parasite maturation. Since the selectivity for several different solutes and the enthalpy of activation of transport remain unaltered with maturation-related increase of permeability, it is concluded that the number of transport agencies in the host cell membrane increases with parasite maturation. Evidence is presented to indicate the need for parasite protein synthesis as an essential factor for the generation of the new permeability pathways.
人类红细胞内疟原虫(恶性疟原虫)会诱导其宿主细胞膜的通透性发生变化。利用寄生虫生长不同阶段受感染红细胞的差异通透性,结合密度梯度离心法,根据发育阶段对寄生细胞进行分级分离。通过这种方法,可以获得基本上由感染最幼龄寄生虫阶段(即环状体)的红细胞组成的细胞级分。这些制剂用于测量各种溶质的转运。结果表明,宿主红细胞膜的通透性在寄生虫侵入红细胞后6小时就开始出现,并随着寄生虫的成熟而逐渐增加。由于几种不同溶质的选择性以及转运的活化焓不会随着与成熟相关的通透性增加而改变,因此得出结论,宿主细胞膜中转运机构的数量会随着寄生虫的成熟而增加。有证据表明,寄生虫蛋白质合成是产生新的通透性途径的必要因素。