Kono Maya, Heincke Dorothee, Wilcke Louisa, Wong Tatianna Wai Ying, Bruns Caroline, Herrmann Susann, Spielmann Tobias, Gilberger Tim W
Department of Cellular Parasitology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg 20359, Germany.
Department of Cellular Parasitology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg 20359, Germany M.G. DeGroote Institute for Infectious Disease Research, Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario L8N 3Z5, Canada.
J Cell Sci. 2016 Feb 15;129(4):673-80. doi: 10.1242/jcs.181230. Epub 2016 Jan 13.
The intraerythrocytic developmental cycle of Plasmodium falciparum is completed with the release of up to 32 invasive daughter cells, the merozoites, into the blood stream. Before release, the final step of merozoite development is the assembly of the cortical pellicle, a multi-layered membrane structure. This unique apicomplexan feature includes the inner membrane complex (IMC) and the parasite's plasma membrane. A dynamic ring structure, referred to as the basal complex, is part of the IMC and helps to divide organelles and abscises in the maturing daughter cells. Here, we analyze the dynamics of the basal complex of P. falciparum. We report on a novel transmembrane protein of the basal complex termed BTP1, which is specific to the genus Plasmodium. It colocalizes with the known basal complex marker protein MORN1 and shows distinct dynamics as well as localization when compared to other IMC proteins during schizogony. Using a parasite plasma membrane marker cell line, we correlate dynamics of the basal complex with the acquisition of the maternal membrane. We show that plasma membrane invagination and IMC propagation are interlinked during the final steps of cell division.
恶性疟原虫的红细胞内发育周期以释放多达32个侵入性子细胞(裂殖子)进入血流而完成。在释放之前,裂殖子发育的最后一步是皮质表膜的组装,这是一种多层膜结构。这种独特的顶复门特征包括内膜复合体(IMC)和寄生虫的质膜。一种被称为基部复合体的动态环状结构是IMC的一部分,有助于细胞器的分裂并在成熟子细胞中脱离。在这里,我们分析了恶性疟原虫基部复合体的动态变化。我们报道了一种基部复合体的新型跨膜蛋白,称为BTP1,它是疟原虫属特有的。它与已知的基部复合体标记蛋白MORN1共定位,并且在裂体增殖期间与其他IMC蛋白相比显示出不同的动态变化和定位。使用寄生虫质膜标记细胞系,我们将基部复合体的动态变化与母体质膜的获取相关联。我们表明,在细胞分裂的最后步骤中,质膜内陷和IMC传播是相互关联的。