Gruenberg J, Allred D R, Sherman I W
J Cell Biol. 1983 Sep;97(3):795-802. doi: 10.1083/jcb.97.3.795.
The nature of the surface deformations of erythrocytes infected with the human malaria parasite Plasmodium falciparum was analyzed using scanning electron microscopy at two stages of the 48-h parasite maturation cycle. Infected cells bearing trophozoite-stage parasites (24-36 h) had small protrusions (knobs), with diameters varying from 160 to 110 nm, and a density ranging from 10 to 35 knobs X micron-2. When parasites were fully mature (schizont stage, 40-44 h), knob size decreased (100-70 nm), whereas density increased (45-70 knobs X micron-2). Size and density of the knobs varied inversely, suggesting that knob production (a) occurred throughout intraerythrocytic parasite development from trophozoite to schizont and (b) was related to dynamic changes of the erythrocyte membrane. Variation in the distribution of the knobs over the red cell surface was observed during parasite maturation. At the early trophozoite stage of parasite development, knobs appeared to be formed in particular domains of the cell surface. As the density of knobs increased and they covered the entire cell surface, their lateral distribution was dispersive (more-than-random); this was particularly evident at the schizont stage. Regional surface patterns of knobs (rows, circles) were seen throughout parasite development. The nature of the dynamic changes that occurred at the red cell surface during knob formation, as well as the nonrandom distribution of knobs, suggested that the red cell cytoskeleton may have played a key role in knob formation and patterning.
在人类疟原虫恶性疟原虫感染红细胞的48小时寄生虫成熟周期的两个阶段,使用扫描电子显微镜分析了红细胞表面变形的性质。带有滋养体阶段寄生虫(24 - 36小时)的感染细胞有小突起(瘤),直径从160到110纳米不等,密度为每平方微米10到35个瘤。当寄生虫完全成熟(裂殖体阶段,40 - 44小时)时,瘤的大小减小(100 - 70纳米),而密度增加(每平方微米45 - 70个瘤)。瘤的大小和密度呈反比变化,这表明瘤的产生(a)在红细胞内寄生虫从滋养体到裂殖体的整个发育过程中都有发生,并且(b)与红细胞膜的动态变化有关。在寄生虫成熟过程中观察到瘤在红细胞表面分布的变化。在寄生虫发育的早期滋养体阶段,瘤似乎在细胞表面的特定区域形成。随着瘤密度的增加并覆盖整个细胞表面,它们的横向分布是分散的(大于随机分布);这在裂殖体阶段尤为明显。在整个寄生虫发育过程中都能看到瘤的区域表面模式(行、圈)。在瘤形成过程中红细胞表面发生的动态变化性质以及瘤的非随机分布表明,红细胞细胞骨架可能在瘤的形成和模式形成中起关键作用。