Barak Efrat, Amin-Spector Sigal, Gerliak Elena, Goyard Sophie, Holland Neta, Zilberstein Dan
Department of Biology, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Mol Biochem Parasitol. 2005 May;141(1):99-108. doi: 10.1016/j.molbiopara.2005.02.004.
Leishmania donovani are the causative agents of kala-azar in humans. They undergo a developmental program following changes in the environment, resulting in the reversible transformation between the extracellular promastigote form in the sand fly vector and the obligatory intracellular amastigote form in phagolysosomes of macrophages. A host-free differentiation system for L. donovani was used to investigate the initial process of promastigote to amastigote differentiation. Within an hour after exposing promastigotes to differentiation signal (concomitant exposure to 37 degrees C and pH 5.5), they expressed the amastigote-specific A2 protein family. At 5 h they started to transform to amastigote-shaped cells, a process that was completed 7 h later. This morphological transformation occurred synchronously, while cells arrested at G1. By sequential exposure to elevated temperature (for 24 h) and then acidic pH, we found that heat was responsible for the growth arrest and acidic pH to its release and subsequent route to differentiation into amastigotes. Lastly, ethanol and Azetidine 2 carboxylic acid (a synthetic proline analog) that induced heat shock response in promastigotes were capable of replacing heat in the differentiation signal.
杜氏利什曼原虫是人类黑热病的病原体。它们会根据环境变化经历一个发育程序,导致在沙蝇载体中的细胞外前鞭毛体形式与巨噬细胞吞噬溶酶体中的 obligatory 细胞内无鞭毛体形式之间发生可逆转变。利用杜氏利什曼原虫的无宿主分化系统来研究前鞭毛体向无鞭毛体分化的初始过程。在前鞭毛体暴露于分化信号(同时暴露于 37 摄氏度和 pH 5.5)后的一小时内,它们表达了无鞭毛体特异性 A2 蛋白家族。在 5 小时时,它们开始转变为无鞭毛体形状的细胞,这一过程在 7 小时后完成。这种形态转变同步发生,而细胞停滞在 G1 期。通过依次暴露于高温(24 小时)然后酸性 pH,我们发现热导致生长停滞,酸性 pH 导致其释放并随后分化为无鞭毛体。最后,在前鞭毛体中诱导热休克反应的乙醇和氮杂环丁烷 2 - 羧酸(一种合成脯氨酸类似物)能够在分化信号中替代热。