Lewis D H, Peters W
Ann Trop Med Parasitol. 1977 Sep;71(3):295-312. doi: 10.1080/00034983.1977.11687192.
Infections of Leishmania mexicana in cultured normal mouse peritoneal macrophages show different morphological features depending on whether the parasites invade as promastigote or amastigote forms. Infections derived from promastigote invasion are characterized by parasitophorous vacuoles which develop slowly, and acquire only modest proportions. In contrast, the organisms in amastigote-derived infections lie within parasitophorous vacuoles which develop more rapidly, and attain a much greater size. From observation of promastigotes of different species of Leishmania, it appeared that survival subsequent to endocytosis by normal macrophages depends on the parasites' rapid transformation to the amastigote form. Activation of the macrophage population produced an enhanced parasiticidal effect only against incompletely transformed Leishmania promastigotes. Electron microscope investigations, involving enzyme histochemistry and lysosome labelling techniques, indicate that intracellular Leishmania avoid digestion by interfering with the activity of lysosomal enzymes that are freely delivered to the parasitophorous vacuole. It is proposed that this ability is acquired on transformation to the amastigote, and incidentally induces fluid distension of the parasitophorous vacuole through phenomena recently described by other workers.
在培养的正常小鼠腹腔巨噬细胞中,墨西哥利什曼原虫感染呈现出不同的形态特征,这取决于寄生虫是以前鞭毛体还是无鞭毛体的形式侵入。前鞭毛体侵入引起的感染特征是,吞噬泡形成缓慢,且体积增长有限。相比之下,无鞭毛体感染中的病原体位于吞噬泡内,吞噬泡形成更快,且体积大得多。通过观察不同种利什曼原虫的前鞭毛体,发现正常巨噬细胞内吞后寄生虫的存活似乎取决于其快速转变为无鞭毛体形式。巨噬细胞群体的激活仅对未完全转变的利什曼原虫前鞭毛体产生增强的杀寄生虫作用。涉及酶组织化学和溶酶体标记技术的电子显微镜研究表明,细胞内的利什曼原虫通过干扰自由输送到吞噬泡的溶酶体酶的活性来避免被消化。有人提出,这种能力是在转变为无鞭毛体时获得的,并且顺便通过其他研究者最近描述的现象诱导吞噬泡的液体膨胀。