Shaw M K
ILRAD, Nairobi, Kenya.
Exp Parasitol. 1999 May;92(1):24-31. doi: 10.1006/expr.1998.4393.
The main conclusion from the present study is that T. parva sporozoite entry is dependent on a functional host cell actin cytoskeleton and is not driven by the parasite. Treating lymphocytes with cytochalasin D resulted in a dose-dependent reduction in the levels of host cell infection. However, the primary effect was to block sporozoite binding and only at the highest concentration (20 microM) was sporozoite internalization significantly reduced. In fact at lower concentrations (1-10 microM) cytochalasin treatment lead to a relative increase in sporozoite internalization. The results are consistent with sporozoite entry being primarily a passive process and with a functional host cell actin cytoskeleton that is required only to maintain the molecular integrity of the surface membrane. Thus T. parva sporozoite entry differs from the process in other apicomplexans, although the results are consistent with a number of features of sporozoite biology. Treatment of lymphocytes with either the microtubule-destabilizing agent, nocodazole, or taxol, which induces microtubule polymerization, had no significant effect on sporozoite binding or entry. As both reagents had the expected effects on the lymphocyte microtubule system, it is unlikely that host cell microtubules are essential for successful sporozoite invasion or establishment.
本研究的主要结论是,泰勒氏巴贝斯虫子孢子进入宿主细胞依赖于功能性的宿主细胞肌动蛋白细胞骨架,而非由寄生虫驱动。用细胞松弛素D处理淋巴细胞会导致宿主细胞感染水平呈剂量依赖性降低。然而,主要作用是阻断子孢子结合,只有在最高浓度(20微摩尔)时子孢子内化才会显著减少。事实上,在较低浓度(1 - 10微摩尔)时,细胞松弛素处理会导致子孢子内化相对增加。这些结果与子孢子进入主要是一个被动过程以及功能性的宿主细胞肌动蛋白细胞骨架仅用于维持表面膜的分子完整性相一致。因此,泰勒氏巴贝斯虫子孢子进入过程与其他顶复门原虫的过程不同,尽管这些结果与子孢子生物学的一些特征相符。用微管破坏剂诺考达唑或诱导微管聚合的紫杉醇处理淋巴细胞,对子孢子结合或进入均无显著影响。由于这两种试剂对淋巴细胞微管系统都产生了预期的作用,宿主细胞微管对于子孢子成功入侵或定植不太可能是必不可少的。