Malaria Group, International Centre for Genetic Engineering and Biotechnology ICGEB, New Delhi, India.
Cell Microbiol. 2013 Jun;15(6):910-21. doi: 10.1111/cmi.12086. Epub 2012 Dec 28.
Egress of Plasmodium falciparum merozoites from host erythrocytes is a critical step in multiplication of blood-stage parasites. A cascade of proteolytic events plays a major role in degradation of membranes leading to egress of merozoites. However, the signals that regulate the temporal activation and/or secretion of proteases upon maturation of merozoites in intra-erythrocytic schizonts remain unclear. Here, we have tested the role of intracellular Ca(2+) in regulation of egress of P. falciparum merozoites from schizonts. A sharp rise in intracellular Ca(2+) just before egress, observed by time-lapse video microscopy, suggested a role for intracellular Ca(2+) in this process. Chelation of intracellular Ca(2+) with chelators such as BAPTA-AM or inhibition of Ca(2+) release from intracellular stores with a phospholipase C (PLC) inhibitor blocks merozoite egress. Interestingly, chelation of intracellular Ca(2+) in schizonts was also found to block the discharge of a key protease PfSUB1 (subtilisin-like protease 1) from exonemes of P. falciparum merozoites to parasitophorous vacuole (PV). This leads to inhibition of processing of PfSERA5 (serine repeat antigen 5) and a block in parasitophorous vacuolar membrane (PVM) rupture and merozoite egress. A complete understanding of the steps regulating egress of P. falciparum merozoites may provide novel targets for development of drugs that block egress and limit parasite growth.
疟原虫裂殖子从宿主红细胞逸出是血期寄生虫繁殖的关键步骤。一系列蛋白水解事件在导致裂殖子逸出的膜降解中起主要作用。然而,在红内期裂殖体中裂殖子成熟时,调节蛋白酶时空激活和/或分泌的信号仍不清楚。在这里,我们测试了细胞内 Ca(2+) 在调节疟原虫裂殖子从裂殖体逸出中的作用。通过延时视频显微镜观察到,逸出前细胞内 Ca(2+) 的急剧上升表明细胞内 Ca(2+) 在这个过程中起作用。螯合细胞内 Ca(2+) 用螯合剂如 BAPTA-AM 或用 PLC 抑制剂抑制细胞内储存库的 Ca(2+) 释放可阻止裂殖子逸出。有趣的是,还发现螯合裂殖体内的细胞内 Ca(2+) 也阻止了关键蛋白酶 PfSUB1(枯草杆菌蛋白酶样蛋白酶 1)从疟原虫裂殖子的外体排出到寄生泡(PV)。这导致 PfSERA5(丝氨酸重复抗原 5)的加工受到抑制,并阻止寄生泡膜(PVM)破裂和裂殖子逸出。对调节疟原虫裂殖子逸出的步骤的全面了解可能为开发阻止逸出和限制寄生虫生长的药物提供新的靶标。