Qu J Q, Shen B G, Wang J Y, Bao Y F, Yang Y T
Institute of Parasitic Diseases, Chinese Academy of Preventive Medicine, Shanghai.
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 1993;11(4):267-9.
The interaction of promastigotes of Leishmania with mouse peritoneal macrophage in vitro was studied by scanning electron microscopy. The results showed that when promastigotes had been incubated with 1/1,000 McAb for 1 h, morphological changes could be seen in most promastigotes, some promastigotes were lysed and some promastigotes although adhered to the macrophage, but no penetration could be seen. When 1/1,000 McAb had been inactivated at 56 degrees C for 1 h and then incubated with promastigotes, scanning electron microscopic examination showed the promastigotes closely adhered to the surface of macrophage with their anterior end "buried" within macrophage. The results of the present study suggested that the mechanism of promastigote-macrophage adhesion was ligand-receptor binding interaction (Figs. 1-11).
用扫描电子显微镜研究了利什曼原虫前鞭毛体与小鼠腹腔巨噬细胞在体外的相互作用。结果显示,当将前鞭毛体与1/1000的单克隆抗体(McAb)孵育1小时后,大多数前鞭毛体可见形态变化,一些前鞭毛体被裂解,一些前鞭毛体虽粘附于巨噬细胞,但未见穿透现象。当1/1000的单克隆抗体在56℃灭活1小时后再与前鞭毛体孵育,扫描电子显微镜检查显示前鞭毛体紧密粘附于巨噬细胞表面,其前端“埋入”巨噬细胞内。本研究结果提示前鞭毛体与巨噬细胞粘附的机制是配体-受体结合相互作用(图1-11)。