Division of Cellular and Applied Infection Biology, Institute of Biology 2, RWTH Aachen University, Aachen, Germany.
Division of Cellular and Applied Infection Biology, Institute of Biology 2, RWTH Aachen University, Aachen, Germany.
Mol Biochem Parasitol. 2021 May;243:111372. doi: 10.1016/j.molbiopara.2021.111372. Epub 2021 May 4.
Malaria parasites are obligate intracellular pathogens that live in human red blood cells harbored by a parasitophorous vacuole. The parasites need to exit from the red blood cell to continue life-cycle progression and ensure human-to-mosquito transmission. Two types of blood stages are able to lyse the enveloping red blood cell to mediate egress, the merozoites and the gametocytes. The intraerythrocytic parasites exit the red blood cell via an inside-out mode during which the membrane of the parasitophorous vacuole ruptures prior to the red blood cell membrane. Membrane rupture is initiated by the exocytosis of specialized secretory vesicles following the perception of egress triggers. The molecular mechanisms of red blood cell egress have particularly been studied in malaria gametocytes. Upon activation by external factors, gametocytes successively discharge at least two types of vesicles, the osmiophilic bodies needed to rupture the parasitophorous vacuole membrane and recently identified egress vesicles that are important for the perforation of the erythrocyte membrane. In recent years, important components of the signaling cascades leading to red blood cell egress have been investigated and several proteins of the osmiophilic bodies have been identified. We here report on the newest findings on the egress of gametocytes from the red blood cell. We further focus on the content and function of the egress-related vesicles and discuss the molecular machinery that might drive vesicle discharge.
疟原虫是专性细胞内寄生虫,生活在被滋养液泡包裹的人类红细胞内。寄生虫需要从红细胞中逸出,以继续生命周期的进展,并确保在人类和蚊子之间传播。两种类型的血期都能够裂解包裹的红细胞以介导逸出,即裂殖子和配子。在红细胞内的寄生虫通过内翻模式从红细胞逸出,在此过程中,滋养液泡的膜在红细胞膜之前破裂。膜破裂是通过专门的分泌囊泡的胞吐作用启动的,这是在感知逸出触发之后发生的。红细胞逸出的分子机制在疟疾配子中得到了特别研究。配子在受到外部因素的激活后,会依次排出至少两种囊泡,一种是需要破裂滋养液泡膜的亲脂体,另一种是最近发现的对于红细胞膜穿孔很重要的逸出囊泡。近年来,导致红细胞逸出的信号级联的重要成分已经被研究,并且已经鉴定出了亲脂体的几种蛋白质。我们在这里报告配子从红细胞中逸出的最新发现。我们进一步关注与逸出相关的囊泡的内容和功能,并讨论可能驱动囊泡排出的分子机制。