Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Apoptosis. 2010 Mar;15(3):376-85. doi: 10.1007/s10495-009-0435-6.
Intracellular pathogens are known to inhibit host cell apoptosis efficiently to ensure their own survival. However, following replication within a cell, they typically need to egress in order to infect new cells. For a long time it was assumed that this happens by simply disrupting the host cell and in some cases, such as for Plasmodium-infected erythrocytes, this seems indeed to be true. However, recently it has been shown that in Plasmodium-infected hepatocytes, an ordered form of cell death is initiated. This cell death is parasite-dependent and can clearly be distinguished from apoptosis and necrosis. The key event, and point of no return, appears to be the rupture of the parasitophorous vacuole membrane (PVM). PVM disruption and host cell death depend on the activation of cysteine proteases. Whether these are of parasite or host cell origin seems to rely on the life cycle stage of the Plasmodium parasite and the corresponding host cell.
细胞内病原体能够有效地抑制宿主细胞凋亡,以确保自身存活。然而,在细胞内复制后,它们通常需要出胞,才能感染新的细胞。长期以来,人们一直认为这是通过简单地破坏宿主细胞来实现的,在某些情况下,例如疟原虫感染的红细胞,这似乎确实是事实。然而,最近的研究表明,在疟原虫感染的肝细胞中,会引发一种有序的细胞死亡形式。这种细胞死亡依赖于寄生虫,并可明显区别于细胞凋亡和坏死。关键事件和不可逆转的点似乎是滋养体空泡膜(PVM)的破裂。PVM 的破坏和宿主细胞的死亡依赖于半胱氨酸蛋白酶的激活。这些蛋白酶是寄生虫还是宿主细胞的来源,似乎取决于疟原虫寄生虫的生命周期阶段和相应的宿主细胞。