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X-Ray Microanalysis Investigation of the Changes in Na K and Hemoglobin Concentration in Plasmodium falciparum-Infected Red Blood Cells

机译:恶性疟原虫感染的红细胞中NaK和血红蛋白浓度变化的X射线显微分析研究

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摘要

Plasmodium falciparum is responsible for severe malaria. During the ∼48 h duration of its asexual reproduction cycle in human red blood cells, the parasite causes profound alterations in the homeostasis of the host red cell, with reversal of the normal Na and K gradients across the host cell membrane, and a drastic fall in hemoglobin content. A question critical to our understanding of how the host cell retains its integrity for the duration of the cycle had been previously addressed by modeling the homeostasis of infected cells. The model predicted a critical contribution of excess hemoglobin consumption to cell integrity (the colloidosmotic hypothesis). Here we tested this prediction with the use of electron-probe x-ray microanalysis to measure the stage-related changes in Na, K, and Fe contents in single infected red cells and in uninfected controls. The results document a decrease in Fe signal with increased Na/K ratio. Interpreted in terms of concentrations, the results point to a sustained fall in host cell hemoglobin concentration with parasite maturation, supporting a colloidosmotic role of excess hemoglobin digestion. The results also provide, for the first time to our knowledge, comprehensive maps of the elemental distributions of Na, K, and Fe in falciparum-infected red blood cells.
机译:恶性疟原虫是导致严重疟疾的原因。在人类红细胞的无性繁殖周期的约48小时内,寄生虫会导致宿主红细胞体内稳态的深刻变化,宿主细胞膜上正常的Na和K梯度会逆转,并急剧下降血红蛋白含量。以前已经通过对受感染细胞的体内稳态进行建模,解决了一个对我们了解宿主细胞在整个周期中如何保持其完整性至关重要的问题。该模型预测了血红蛋白消耗过多对细胞完整性的重要贡献(胶体渗透假说)。在这里,我们使用电子探针X射线显微分析法测试了这一预测,以测量单个感染红细胞和未感染对照中Na,K和Fe含量与阶段相关的变化。结果表明,Fe信号随Na / K比的增加而降低。从浓度的角度解释,结果表明宿主细胞血红蛋白浓度持续下降,并伴有寄生虫成熟,支持了过多血红蛋白消化的胶体渗透作用。该结果还首次为我们所知,提供了恶性疟原虫感染的红细胞中Na,K和Fe元素分布的综合图。

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