The malaria sporozoite's journey into the liver.

Infectious agents and disease Pub Date : 1996-06-01
P Sinnis
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Abstract

Perhaps the most challenging event of the malaria parasite's lifecycle is the sporozoite's journey to the hepatocyte. Because few parasites are injected by the mosquito, they must be efficiently and rapidly targeted to hepatocytes, where they will invade and develop into merozoites, the form of the parasite infective for red blood cells. Little is known about how sporozoites make their way to the liver and subsequently invade hepatocytes. Some evidence suggests that they are initially trapped by Kupffer cells and then transported to hepatocytes. Other findings support the hypothesis that sporozoites home to hepatocytes directly. We have found that the major surface protein of malaria sporozoites, the CS protein, binds to the basolateral domain of hepatocytes and, when injected intravenously into mice, is rapidly cleared from the circulation by the liver. Whether sporozoites are arrested in the liver by the same mechanisms as CS protein is not known, although preliminary data suggests this may be the case. Other sporozoite proteins are also likely to be involved in hepatocyte invasion. TRAP or SSP2, found on the parasite surface and in micronemes, binds to hepatocytes in a similar pattern as CS protein. There is evidence demonstrating its involvement in invasion, although it is not known whether it functions in the initial sequestration of the parasites by the liver or in subsequent invasion events.

疟疾孢子进入肝脏的过程。
也许疟疾寄生虫生命周期中最具挑战性的事件是孢子子进入肝细胞的旅程。因为蚊子注射的寄生虫很少,所以它们必须有效而迅速地靶向肝细胞,在那里它们会侵入并发育成分裂子,这是一种感染红细胞的寄生虫。关于孢子子如何进入肝脏并随后侵入肝细胞,我们知之甚少。一些证据表明,它们最初被库普弗细胞捕获,然后被运送到肝细胞。其他的研究结果支持了孢子子直接进入肝细胞的假设。我们发现,疟疾孢子子的主要表面蛋白CS蛋白与肝细胞的基底外侧结构域结合,当静脉注射到小鼠体内时,它会被肝脏迅速从循环中清除。尽管初步数据表明可能是这种情况,但尚不清楚孢子体是否通过与CS蛋白相同的机制在肝脏中被抑制。其他的子孢子蛋白也可能参与肝细胞的侵袭。TRAP或SSP2在寄生虫表面和微素中发现,以与CS蛋白相似的模式与肝细胞结合。有证据表明它参与了入侵,尽管尚不清楚它是否在肝脏对寄生虫的初始隔离中起作用,还是在随后的入侵事件中起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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