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疟原虫在红细胞外期发育过程中寄生虫质膜和寄生泡膜的变化。

Alteration of the parasite plasma membrane and the parasitophorous vacuole membrane during exo-erythrocytic development of malaria parasites.

作者信息

Sturm Angelika, Graewe Stefanie, Franke-Fayard Blandine, Retzlaff Silke, Bolte Stefanie, Roppenser Bernhard, Aepfelbacher Martin, Janse Chris, Heussler Volker

机构信息

Bernhard Nocht Institute For Tropical Medicine, Bernhard-Nocht-Str. 74, 20359 Hamburg, Germany.

出版信息

Protist. 2009 Feb;160(1):51-63. doi: 10.1016/j.protis.2008.08.002. Epub 2008 Nov 20.

Abstract

The rodent malaria parasite Plasmodium berghei develops in hepatocytes within 48-52h from a single sporozoite into up to 20,000 daughter parasites, so-called merozoites. The cellular and molecular details of this extensive proliferation are still largely unknown. Here we have used a transgenic, RFP-expressing P. berghei parasite line and molecular imaging techniques including intravital microscopy to decipher various aspects of parasite development within the hepatocyte. In late schizont stages, MSP1 is expressed and incorporated into the parasite plasma membrane that finally forms the membrane of developing merozoites by continuous invagination steps. We provide first evidence for activation of a verapamil-sensitive Ca(2+) channel in the plasma membrane of liver stage parasites before invagination occurs. During merozoite formation, the permeability of the parasitophorous vacuole membrane changes considerably before it finally becomes completely disrupted, releasing merozoites into the host cell cytoplasm.

摘要

啮齿动物疟原虫伯氏疟原虫在48 - 52小时内从单个子孢子在肝细胞内发育成多达20000个子代寄生虫,即所谓的裂殖子。这种广泛增殖的细胞和分子细节在很大程度上仍然未知。在这里,我们使用了一种表达红色荧光蛋白(RFP)的转基因伯氏疟原虫寄生虫株以及包括活体显微镜在内的分子成像技术,来解读寄生虫在肝细胞内发育的各个方面。在晚期裂殖体阶段,裂殖子表面蛋白1(MSP1)表达并整合到寄生虫质膜中,该质膜最终通过连续内陷步骤形成发育中裂殖子的膜。我们首次提供证据表明,在发生内陷之前,肝期寄生虫质膜中的一种维拉帕米敏感钙通道被激活。在裂殖子形成过程中,寄生泡膜的通透性在最终完全破裂之前发生了相当大的变化,从而将裂殖子释放到宿主细胞细胞质中。

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