Pimenta P F, De Souza W
J Submicrosc Cytol. 1986 Jan;18(1):127-32.
Acid phosphatase was cytochemically detected at the ultrastructural level in infective and non-infective promastigotes and in amastigotes of the parasitic protozoan Leishmania mexicana amazonensis. Cerium chloride was used as the capture agent of the phosphate liberated during the hydrolysis of the substrate (Na-beta-glycerophosphate). Reaction product, indicative of enzyme activity, was seen in the outer face of the plasma membrane of many, but not all, infective and noninfective promastigote forms. No reaction product was seen in the plasma membrane of amastigote forms. Reaction product was seen in the endoplasmic reticulum, in the Golgi complex, in vesicles located close to the flagellar pocket and in cytoplasmic structures which may represent lysosomes. No reaction product was seen when the substrate was omitted from or sodium fluoride was added to the incubation medium. The possible role played by the acid phosphatase present in the plasma membrane of Leishmania parasites is discussed.
在感染性和非感染性前鞭毛体以及亚马逊利什曼原虫无鞭毛体的超微结构水平上,通过细胞化学方法检测了酸性磷酸酶。氯化铈用作底物(β-甘油磷酸钠)水解过程中释放的磷酸盐的捕获剂。在许多(但不是所有)感染性和非感染性前鞭毛体形式的质膜外表面可见指示酶活性的反应产物。在无鞭毛体形式的质膜中未见反应产物。在内质网、高尔基体、靠近鞭毛袋的小泡以及可能代表溶酶体的细胞质结构中可见反应产物。当从孵育培养基中省略底物或添加氟化钠时,未见反应产物。讨论了利什曼原虫寄生虫质膜中存在的酸性磷酸酶可能发挥的作用。