Handman E, Spira D T
Z Parasitenkd. 1977 Aug 25;53(1):75-81. doi: 10.1007/BF00383117.
An in vitro system of prolonged culture of Leishmania tropica amastigotes in mouse macrophages is presented. The division rate of parasites was monitored by microscopic observations and by 3H-thymidine incorporation. The dynamics of macrophage infection and parasite division are influenced by the initial rate of promastigotes per cells in culture. Parasites multiply, gradually infect and finally destroy all available macrophages from normal mice releasing large numbers of viable amastigotes. Macrophages from immune donors were inferior in their ability to support parasite multiplication and did not survive long periods in culture.
本文介绍了一种在小鼠巨噬细胞中对热带利什曼原虫无鞭毛体进行长期培养的体外系统。通过显微镜观察和3H-胸腺嘧啶核苷掺入来监测寄生虫的分裂率。培养物中每个细胞前鞭毛体的初始接种率会影响巨噬细胞感染和寄生虫分裂的动态过程。寄生虫大量繁殖,逐渐感染并最终破坏来自正常小鼠的所有可用巨噬细胞,释放出大量活的无鞭毛体。来自免疫供体的巨噬细胞在支持寄生虫繁殖的能力方面较差,并且在培养中存活时间不长。