Lanar D E
J Protozool. 1979 Aug;26(3):457-62. doi: 10.1111/j.1550-7408.1979.tb04653.x.
Trypanosoma cruzi strain Peru was cultivated in the presence of an established cell line of Triatoma infestans embryo cells (TI- 32). Bloodstream trypomastigotes differentiated into amastigote-like cells (first differentiation phase) which multiplied to form large clusters of cells. Because of their clustering nature, a new term, "staphylomastigotes," has been proposed for this stage. After 10 days of cultivation, 90% of the staphylomastigotes underwent differentiation (2nd differentiation phase) to trypomastigotes (approximately 98%) or epimastigotes (approximately 2%). Bloodstream trypomastigotes cultivated without TI-32 cells underwent the first, but not the 2nd differentiation phase, although occasional epimastogotes were seen (less than 1%). The evidence presented suggests that TI-32 cells produce a labile factor(s) important not only for initiation of the 2nd differentiation phase but also for maintaining the parasites in the trypomastigote stage. The pH of the culture medium was not the initiating factor for the 2nd differentiation phase. Infectivity studies indicated that staphylomastigotes were as infective as blood stream trypomastigotes, but that metacyclic trypomastigotes isolated from culture after the 2nd differentiation phase were slightly more infective than bloodstream forms. Electromicrographs of styphylomastigotes do not provide any evidence of exchange of genetic material between cells.
克氏锥虫秘鲁株在已建立的大锥蝽胚胎细胞系(TI - 32)存在的情况下进行培养。血流型锥鞭毛虫分化为类无鞭毛体细胞(第一分化阶段),这些细胞增殖形成大的细胞簇。由于它们的聚集特性,为此阶段提出了一个新术语“葡萄状无鞭毛体”。培养10天后,90%的葡萄状无鞭毛体经历分化(第二分化阶段)成为锥鞭毛虫(约98%)或上鞭毛体(约2%)。在没有TI - 32细胞的情况下培养的血流型锥鞭毛虫经历了第一分化阶段,但没有经历第二分化阶段,尽管偶尔能看到上鞭毛体(少于1%)。所提供的证据表明,TI - 32细胞产生一种不稳定因子,该因子不仅对启动第二分化阶段很重要,而且对将寄生虫维持在锥鞭毛虫阶段也很重要。培养基的pH值不是第二分化阶段的起始因子。感染性研究表明,葡萄状无鞭毛体与血流型锥鞭毛虫的感染性相同,但从第二分化阶段后的培养物中分离出的循环后期锥鞭毛虫比血流型形态的感染性略高。葡萄状无鞭毛体的电子显微镜照片未提供细胞间遗传物质交换的任何证据。