首页> 外文期刊>Blood: The Journal of the American Society of Hematology >A spiral scaffold underlies cytoadherent knobs in Plasmodium falciparum-infected erythrocytes
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A spiral scaffold underlies cytoadherent knobs in Plasmodium falciparum-infected erythrocytes

机译:螺旋支架位于恶性疟原虫感染的红细胞中细胞粘附旋钮的下方

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摘要

Much of the virulence of Plasmodium falciparum malaria is caused by cytoadherence of infected erythrocytes, which promotes parasite survival by preventing clearance in the spleen. Adherence is mediated by membrane protrusions known as knobs, whose formation depends on the parasite-derived, knob-associated histidine-rich protein (KAHRP). Knobs are required for cytoadherence under flow conditions, and they contain both KAHRP and the parasite-derived erythrocyte membrane protein PfEMP1. Using electron tomography, we have examined the 3-dimensional structure of knobs in detergent-insoluble skeletons of P falciparum 3D7 schizonts. We describe a highly organized knob skeleton composed of a spiral structure coated by an electron-dense layer underlying the knobmembrane. This knob skeleton is connected by multiple links to the erythrocyte cytoskeleton. We used immuno-electron microscopy (EM) to locate KAHRP in these structures. The arrangement of membrane proteins in the knobs, visualized by high-resolution freeze-fracture scanning EM, is distinct from that in the surrounding erythrocyte membrane, with a structure at the apex that likely represents the adhesion site. Thus, erythrocyte knobs in P falciparum infection contain a highly organized skeleton structure underlying a specialized region of membrane. We propose that the spiral and dense coat organize the cytoadherence structures in the knob, and anchor them into the erythrocyte cytoskeleton. The high density of knobs and their extensive mechanical linkage suggest an explanation for the rigidification of the cytoskeleton in infected cells, and for the transmission to the cytoskeleton of shear forces experienced by adhering cells.
机译:恶性疟原虫疟疾的大部分毒力是由感染的红细胞的细胞粘附引起的,它通过防止脾脏清除而促进了寄生虫的生存。粘附是通过称为突起的膜突起来介导的,突起的形成取决于寄生虫衍生的,与突起相关的富含组氨酸的蛋白质(KAHRP)。流动条件下的细胞粘附需要旋钮,并且旋钮同时包含KAHRP和寄生虫衍生的红细胞膜蛋白PfEMP1。使用电子断层扫描,我们已经检查了恶性疟原虫3D7裂殖体的去污剂不溶性骨架中纽结的3维结构。我们描述了高度组织化的旋钮骨架,该骨架由螺旋结构组成,该螺旋结构由位于旋钮膜下面的电子致密层覆盖。该旋钮骨架通过多个链接连接到红细胞的细胞骨架。我们使用免疫电子显微镜(EM)在这些结构中定位KAHRP。通过高分辨率的冷冻断裂扫描EM可视化旋钮中膜蛋白的排列方式,其与周围红细胞膜的排列方式不同,其顶点结构可能代表粘附位点。因此,恶性疟原虫感染中的红血球节含有高度组织化的骨架结构,位于膜的特定区域之下。我们建议螺旋状和致密的外套组织在旋钮中的细胞粘附结构,并将其锚定到红细胞的细胞骨架中。旋钮的高密度及其广泛的机械联系为感染细胞中细胞骨架的僵化以及粘附细胞所经历的剪切力向细胞骨架的传递提供了解释。

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