Day K P, Hayward R E, Smith D, Culvenor J G
Wellcome Trust Centre for Epidemiology of Infectious Disease, Department of Zoology, University of Oxford.
Mol Biochem Parasitol. 1998 Jun 1;93(2):167-77. doi: 10.1016/s0166-6851(98)00040-1.
Plasmodium falciparum trophozoites sequester from the peripheral circulation by adherence to host endothelium. Gametocytes, also sequester during maturation. Analysis of the adhesion phenotype of stage I to V gametocytes of several isolates/clones was assessed by binding of infected cells to C32 melanoma cells (C32MC) and the purified adhesion proteins, leucocyte differentiation antigen (CD36) and intercellular adhesion molecule-1 (ICAM-1). These cells and proteins, have previously been shown to be receptors for adherence of trophozoites. Early gametocytes (stages I-IIA) were found to bind to C32MC as well as the purified receptor CD36 but not to ICAM-1. Early gametocytes bound to C32MC via CD36 and the parasite ligand involved in this binding was trypsin sensitive. Stage IIB to V gametocytes did not adhere to C32MC, CD36 nor ICAM-1. Electron-dense protruberances known as knobs and histidine rich protein 1 (HRP 1) expression have been associated with trophozite adhesion to CD36. Knobs were present at the surface of early but not late gametocyte infected cells. Stage-specific patterns of HRP 1 expression, consistent with a role for this molecule in CD36 adhesion of early gametocytes, were also observed. The adhesion phenotype of these young gametocytes was indistinguishable from that of the trophozoites by all criteria examined. These data support the hypothesis that other host receptors mediate the binding of late gametocytes.
恶性疟原虫滋养体通过黏附于宿主内皮细胞而从外周循环中滞留。配子体在成熟过程中也会滞留。通过感染细胞与C32黑色素瘤细胞(C32MC)以及纯化的黏附蛋白、白细胞分化抗原(CD36)和细胞间黏附分子-1(ICAM-1)的结合,对几种分离株/克隆的I至V期配子体的黏附表型进行了分析。这些细胞和蛋白先前已被证明是滋养体黏附的受体。发现早期配子体(I-IIA期)可与C32MC以及纯化的受体CD36结合,但不与ICAM-1结合。早期配子体通过CD36与C32MC结合,参与这种结合的寄生虫配体对胰蛋白酶敏感。IIB至V期配子体不黏附于C32MC、CD36或ICAM-1。称为小结的电子致密突起和富含组氨酸的蛋白1(HRP 1)表达与滋养体对CD36的黏附有关。小结存在于早期但不存在于晚期配子体感染细胞的表面。还观察到HRP 1表达的阶段特异性模式与该分子在早期配子体CD36黏附中的作用一致。通过所有检测标准,这些年轻配子体的黏附表型与滋养体的黏附表型无法区分。这些数据支持了其他宿主受体介导晚期配子体结合的假说。