Sinnis P
Department of Medical and Molecular Parasitology, New York University Medical Center, NY 10016, USA.
Infect Agents Dis. 1996 Jun;5(3):182-9.
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.
疟原虫生命周期中或许最具挑战性的环节是子孢子前往肝细胞的过程。由于蚊子注入的寄生虫数量很少,它们必须高效且迅速地靶向肝细胞,在那里它们将侵入并发育成裂殖子,即对红细胞具有感染性的寄生虫形态。关于子孢子如何前往肝脏并随后侵入肝细胞,人们知之甚少。一些证据表明,它们最初被库普弗细胞捕获,然后被转运至肝细胞。其他研究结果支持子孢子直接归巢至肝细胞的假说。我们发现,疟原虫子孢子的主要表面蛋白,即环子孢子蛋白(CS蛋白),可与肝细胞的基底外侧结构域结合,并且当静脉注射到小鼠体内时,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,但尚不清楚子孢子是否通过与CS蛋白相同的机制在肝脏中滞留。其他子孢子蛋白也可能参与肝细胞的侵入过程。在寄生虫表面和微线体中发现的跨膜蛋白(TRAP)或子孢子表面蛋白2(SSP2),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侵入过程,尽管尚不清楚它是在肝脏对寄生虫的初始扣押中发挥作用,还是在随后的侵入事件中发挥作用。