Literature DB >> 21402025

X-ray microanalysis investigation of the changes in Na, K, and hemoglobin concentration in plasmodium falciparum-infected red blood cells.

Jakob M A Mauritz1, Rachel Seear, Alessandro Esposito, Clemens F Kaminski, Jeremy N Skepper, Alice Warley, Virgilio L Lew, Teresa Tiffert.   

Abstract

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.
Copyright © 2011 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21402025      PMCID: PMC3059598          DOI: 10.1016/j.bpj.2011.02.007

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  37 in total

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2.  Concentration from continuous culture of erythrocytes infected with trophozoites and schizonts of Plasmodium falciparum.

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Journal:  Ann Trop Med Parasitol       Date:  1978-02

Review 4.  New permeability pathways induced by the malarial parasite in the membrane of its host erythrocyte: potential routes for targeting of drugs into infected cells.

Authors:  H Ginsburg; W D Stein
Journal:  Biosci Rep       Date:  1987-06       Impact factor: 3.840

5.  Digestion of the host erythrocyte by malaria parasites is the primary target for quinoline-containing antimalarials.

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6.  Human malaria parasites in continuous culture.

Authors:  W Trager; J B Jensen
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9.  Alterations of red blood cell sodium transport during malarial infection.

Authors:  M J Dunn
Journal:  J Clin Invest       Date:  1969-04       Impact factor: 14.808

10.  Ionic and osmotic equilibria of human red blood cells treated with nystatin.

Authors:  J C Freedman; J F Hoffman
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Review 3.  Why do malaria parasites increase host erythrocyte permeability?

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8.  A kinetic fluorescence assay reveals unusual features of Ca⁺⁺ uptake in Plasmodium falciparum-infected erythrocytes.

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