Tomlinson S, Vandekerckhove F, Frevert U, Nussenzweig V
Michael Heidelberger Division of Immunology, Department of Pathology, New York University Medical Center, NY 10016, USA.
Parasitology. 1995 Jun;110 ( Pt 5):547-54. doi: 10.1017/s0031182000065264.
Following cell invasion, Trypanosoma cruzi trypomastigotes transform into amastigotes, which are the mammalian replicative forms of the parasite. Although amastigotes represent a critical stage in the life-cycle of T. cruzi, little is known of the factors controlling trypomastigote to amastigote transformation. Kanbera et al. (1990) observed that exposure of trypomastigotes to acidic pH induced their transformation into rounded forms resembling amastigotes. We confirm their observation and, using two strains of T. cruzi, establish that these transformants are ultrastructurally and biochemically indistinguishable from natural amastigotes. Incubation of trypomastigotes in medium at pH 5.0 for 2 h was sufficient to trigger their transformation into forms resembling amastigotes. Electron microscopical analysis confirmed that the kinetoplast structure, and general morphological features of the acid-induced, extracellular amastigotes were indistinguishable from those of intracellular-derived amastigotes. The extracellular transformation was accompanied by the acquisition of the stage-specific surface antigen of the naturally transformed amastigotes (Ssp-4), and loss of a stage-specific trypomastigote antigen (Ssp-3). Trypomastigotes incubated at neutral pH did not transform into amastigotes, and did not acquire the Ssp-4 epitope or lose the Ssp-3 epitope. Finally, acid-induced amastigotes subsequently incorporated [3H]thymidine into their DNA, indicating that the important replicative property of intracellular amastigotes is also exhibited by these in vitro transformants. This effect of low pH appears to be of physiological relevance, and acid-induced extracellular transformation appears to represent a valid experimental technique for studies of the molecular mechanisms involved in the differentiation process.
在细胞入侵后,克氏锥虫锥鞭毛体转变为无鞭毛体,无鞭毛体是该寄生虫在哺乳动物体内的增殖形式。尽管无鞭毛体是克氏锥虫生命周期中的关键阶段,但对于控制锥鞭毛体向无鞭毛体转变的因素却知之甚少。坎贝拉等人(1990年)观察到,将锥鞭毛体暴露于酸性pH值会诱导它们转变为类似无鞭毛体的圆形形态。我们证实了他们的观察结果,并使用两株克氏锥虫确定,这些转化体在超微结构和生化方面与天然无鞭毛体无法区分。将锥鞭毛体在pH 5.0的培养基中孵育2小时足以触发它们转变为类似无鞭毛体的形态。电子显微镜分析证实,酸诱导的细胞外无鞭毛体的动基体结构和一般形态特征与细胞内衍生的无鞭毛体无法区分。细胞外转化伴随着天然转化的无鞭毛体阶段特异性表面抗原(Ssp-4)的获得,以及阶段特异性锥鞭毛体抗原(Ssp-3)的丧失。在中性pH值下孵育的锥鞭毛体不会转变为无鞭毛体,也不会获得Ssp-4表位或失去Ssp-3表位。最后,酸诱导的无鞭毛体随后将[3H]胸腺嘧啶核苷掺入其DNA中,这表明这些体外转化体也表现出细胞内无鞭毛体重要的增殖特性。低pH值的这种作用似乎具有生理相关性,酸诱导的细胞外转化似乎代表了一种用于研究分化过程中分子机制的有效实验技术。