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恶性疟原虫无性生命周期内质网、线粒体和顶质体的发育

Development of the endoplasmic reticulum, mitochondrion and apicoplast during the asexual life cycle of Plasmodium falciparum.

作者信息

van Dooren Giel G, Marti Matthias, Tonkin Christopher J, Stimmler Luciana M, Cowman Alan F, McFadden Geoffrey I

机构信息

Plant Cell Biology Research Centre, School of Botany, University of Melbourne, Parkville, VIC 3010, Australia.

出版信息

Mol Microbiol. 2005 Jul;57(2):405-19. doi: 10.1111/j.1365-2958.2005.04699.x.

Abstract

Plasmodium parasites are unicellular eukaryotes that undergo a series of remarkable morphological transformations during the course of a multistage life cycle spanning two hosts (mosquito and human). Relatively little is known about the dynamics of cellular organelles throughout the course of these transformations. Here we describe the morphology of three organelles (endoplasmic reticulum, apicoplast and mitochondrion) through the human blood stages of the parasite life cycle using fluorescent reporter proteins fused to organelle targeting sequences. The endoplasmic reticulum begins as a simple crescent-shaped organelle that develops into a perinuclear ring with two small protrusions, followed by transformation into an extensive reticulated network as the parasite enlarges. Similarly, the apicoplast and the mitochondrion grow from single, small, discrete organelles into highly branched structures in later-stage parasites. These branched structures undergo an ordered fission - apicoplast followed by mitochondrion - to create multiple daughter organelles that are apparently linked as pairs for packaging into daughter cells. This is the first in-depth examination of intracellular organelles in live parasites during the asexual life cycle of this important human pathogen.

摘要

疟原虫是单细胞真核生物,在跨越两个宿主(蚊子和人类)的多阶段生命周期中会经历一系列显著的形态转变。在这些转变过程中,人们对细胞器的动态变化了解相对较少。在这里,我们使用与细胞器靶向序列融合的荧光报告蛋白,描述了疟原虫生命周期中人类血液阶段三种细胞器(内质网、顶质体和线粒体)的形态。内质网最初是一个简单的新月形细胞器,发展成一个带有两个小突起的核周环,随后随着寄生虫的增大转变为广泛的网状网络。同样,顶质体和线粒体从单个、小的、离散的细胞器生长为后期寄生虫中的高度分支结构。这些分支结构经历有序分裂——先顶质体后线粒体——以产生多个子细胞器,这些子细胞器显然成对连接,以便包装到子细胞中。这是对这种重要人类病原体无性生命周期中活寄生虫内细胞器的首次深入研究。

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