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使用扩展显微镜的红细胞内发育图谱。

Atlas of intraerythrocytic development using expansion microscopy.

机构信息

Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, United States.

Biological and Biomedical Sciences, Harvard Medical School, Boston, United States.

出版信息

Elife. 2023 Dec 18;12:RP88088. doi: 10.7554/eLife.88088.

DOI:10.7554/eLife.88088
PMID:38108809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10727503/
Abstract

Apicomplexan parasites exhibit tremendous diversity in much of their fundamental cell biology, but study of these organisms using light microscopy is often hindered by their small size. Ultrastructural expansion microscopy (U-ExM) is a microscopy preparation method that physically expands the sample by ~4.5×. Here, we apply U-ExM to the human malaria parasite during the asexual blood stage of its lifecycle to understand how this parasite is organized in three dimensions. Using a combination of dye-conjugated reagents and immunostaining, we have cataloged 13 different structures or organelles across the intraerythrocytic development of this parasite and made multiple observations about fundamental parasite cell biology. We describe that the outer centriolar plaque and its associated proteins anchor the nucleus to the parasite plasma membrane during mitosis. Furthermore, the rhoptries, Golgi, basal complex, and inner membrane complex, which form around this anchoring site while nuclei are still dividing, are concurrently segregated and maintain an association to the outer centriolar plaque until the start of segmentation. We also show that the mitochondrion and apicoplast undergo sequential fission events while maintaining an association with the outer centriolar plaque during cytokinesis. Collectively, this study represents the most detailed ultrastructural analysis of during its intraerythrocytic development to date and sheds light on multiple poorly understood aspects of its organelle biogenesis and fundamental cell biology.

摘要

锥虫类寄生虫在其大部分基础细胞生物学中表现出巨大的多样性,但由于其体积小,使用光学显微镜研究这些生物体常常受到阻碍。超微结构扩展显微镜(U-ExM)是一种显微镜制备方法,通过物理方式将样品扩展约 4.5 倍。在这里,我们将 U-ExM 应用于人类疟原虫在其生命周期的无性血阶段,以了解这种寄生虫如何在三维空间中组织。通过结合染料偶联试剂和免疫染色,我们在寄生虫的整个红细胞内发育过程中对 13 种不同的结构或细胞器进行了编目,并对基本寄生虫细胞生物学进行了多次观察。我们描述了外中心粒斑及其相关蛋白在有丝分裂过程中将核锚定到寄生虫质膜上。此外,当核仍在分裂时,形成于该锚定点周围的棒状体、高尔基体、基底复合物和内膜复合物被同时分隔开,并与外中心粒斑保持联系,直到开始分段。我们还表明,线粒体和顶质体在与外中心粒斑保持关联的同时经历了连续的裂变事件,在胞质分裂过程中。总的来说,这项研究代表了迄今为止对疟原虫在其红细胞内发育过程中最详细的超微结构分析,并揭示了其细胞器发生和基本细胞生物学的多个尚未被充分了解的方面。

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