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冷冻传输 X 射线成像技术在疟原虫,恶性疟原虫中的应用。

Cryo transmission X-ray imaging of the malaria parasite, P. falciparum.

机构信息

Electron Microscopy Unit Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, VIC 3010, Australia.

出版信息

J Struct Biol. 2011 Jan;173(1):161-8. doi: 10.1016/j.jsb.2010.08.013. Epub 2010 Sep 6.

Abstract

Cryo transmission X-ray microscopy in the "water window" of photon energies has recently been introduced as a method that exploits the natural contrast of biological samples. We have used cryo tomographic X-ray imaging of the intra-erythrocytic malaria parasite, Plasmodium falciparum, to undertake a survey of the cellular features of this important human pathogen. We examined whole hydrated cells at different stages of growth and defined some of the structures with different X-ray density, including the parasite nucleus, cytoplasm, digestive vacuole and the hemoglobin degradation product, hemozoin. As the parasite develops from an early cup-shaped morphology to a more rounded shape, puncta of hemozoin are formed; these coalesce in the mature trophozoite into a central compartment. In some trophozoite stage parasites we observed invaginations of the parasite surface and, using a selective permeabilization process, showed that these remain connected to the RBC cytoplasm. Some of these invaginations have large openings consistent with phagocytic structures and we observed independent endocytic vesicles in the parasite cytoplasm which appear to play a role in hemoglobin uptake. In schizont stage parasites staggered mitosis was observed and X-ray-dense lipid-rich structures were evident at their apical ends of the developing daughter cells. Treatment of parasites with the antimalarial drug artemisinin appears to affect parasite development and their ability to produce the hemoglobin breakdown product, hemozoin.

摘要

近年来,利用生物样品天然对比度的光子能量“水窗”中的冷冻传输 X 射线显微镜已被引入作为一种方法。我们使用冷冻断层成像 X 射线成像技术对疟原虫(Plasmodium falciparum)进行了红细胞内寄生虫的研究,以调查这种重要的人类病原体的细胞特征。我们检查了不同生长阶段的整个水合细胞,并定义了一些具有不同 X 射线密度的结构,包括寄生虫核、细胞质、消化液泡和血红蛋白降解产物疟色素。随着寄生虫从早期杯状形态发展到更圆的形状,疟色素的斑点形成;在成熟的滋养体中,这些斑点合并成一个中央隔室。在一些滋养体阶段的寄生虫中,我们观察到寄生虫表面的内陷,并使用选择性渗透处理过程表明,这些内陷仍然与 RBC 细胞质相连。这些内陷中的一些具有与吞噬结构一致的大开口,我们观察到寄生虫细胞质中的独立内吞小泡,这些小泡似乎在血红蛋白摄取中发挥作用。在裂殖体阶段的寄生虫中观察到交错的有丝分裂,并且在发育中的子细胞的顶端可以看到富含脂质的 X 射线密集结构。抗疟药物青蒿素的处理似乎会影响寄生虫的发育及其产生血红蛋白分解产物疟色素的能力。

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本文引用的文献

1
Artemisinin directly targets malarial mitochondria through its specific mitochondrial activation.
PLoS One. 2010 Mar 8;5(3):e9582. doi: 10.1371/journal.pone.0009582.
2
Digestive-vacuole genesis and endocytic processes in the early intraerythrocytic stages of Plasmodium falciparum.
J Cell Sci. 2010 Feb 1;123(Pt 3):441-50. doi: 10.1242/jcs.061499. Epub 2010 Jan 12.
3
Soft X-ray tomography of phenotypic switching and the cellular response to antifungal peptoids in Candida albicans.
Proc Natl Acad Sci U S A. 2009 Nov 17;106(46):19375-80. doi: 10.1073/pnas.0906145106. Epub 2009 Oct 30.
4
Soft X-ray tomography and cryogenic light microscopy: the cool combination in cellular imaging.
Trends Cell Biol. 2009 Nov;19(11):587-95. doi: 10.1016/j.tcb.2009.08.005. Epub 2009 Oct 7.
5
The malaria merozoite, forty years on.
Parasitology. 2009 Oct;136(12):1435-44. doi: 10.1017/S0031182009990734. Epub 2009 Aug 3.
7
High-resolution X-ray imaging of Plasmodium falciparum-infected red blood cells.
Cytometry A. 2008 Oct;73(10):949-57. doi: 10.1002/cyto.a.20616.
8
Plasmodium in the postgenomic era: new insights into the molecular cell biology of malaria parasites.
Int Rev Cell Mol Biol. 2008;266:85-156. doi: 10.1016/S1937-6448(07)66003-1.
9
A new model for hemoglobin ingestion and transport by the human malaria parasite Plasmodium falciparum.
J Cell Sci. 2008 Jun 1;121(11):1937-49. doi: 10.1242/jcs.023150. Epub 2008 May 13.
10
The Maurer's cleft protein MAHRP1 is essential for trafficking of PfEMP1 to the surface of Plasmodium falciparum-infected erythrocytes.
Mol Microbiol. 2008 Jun;68(5):1300-14. doi: 10.1111/j.1365-2958.2008.06235.x. Epub 2008 Apr 11.

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