Literature DB >> 2651918

A study of red cell membrane properties in relation to malarial invasion.

K Rangachari1, G H Beaven, G B Nash, B Clough, A R Dluzewski, R J Wilson, W B Gratzer.   

Abstract

The shape and mechanical properties of human red cells were modified in several ways and the consequences for the efficiency of invasion by Plasmodium falciparum in culture were investigated. Inhibition of invasion by depletion of ATP was shown to be unrelated to cell shape or deformability changes. Treatment of cells with N-ethylmaleimide (NEM), which dissociates some 70% of the native spectrin tetramers into the dimer, grossly reduced deformation of the cells under shear and increased by a factor of two or more the shear elastic modulus, as measured by the micropipette aspiration technique. Cells thus treated were efficiently invaded by P. falciparum (ca. 75% of control). In a population of cells pretreated with chlorpromazine, parasites were found in stomatocytic cells which were highly undeformable under shear. There was also considerable invasion into cells from subjects with hereditary pyropoikilocytosis, and two types of elliptocytosis. Cells treated with wheat germ agglutinin showed a dose-dependent increase in rigidity; a fivefold increase in elastic modulus (with total loss of deformation under shear in our conditions) still permitted invasion at a level of 50% of the control. The results suggest that gross mechanical properties of the membrane per se, at least within any physiologically relevant range, are unlikely to be the primary determinant of malarial invasion; this may instead be linked to the freedom of membrane proteins to migrate in the course of entry of the parasite.

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Year:  1989        PMID: 2651918     DOI: 10.1016/0166-6851(89)90020-0

Source DB:  PubMed          Journal:  Mol Biochem Parasitol        ISSN: 0166-6851            Impact factor:   1.759


  6 in total

1.  Elasticity of the red cell membrane and its relation to hemolytic disorders: an optical tweezers study.

Authors:  J Sleep; D Wilson; R Simmons; W Gratzer
Journal:  Biophys J       Date:  1999-12       Impact factor: 4.033

2.  Delivery of the malaria virulence protein PfEMP1 to the erythrocyte surface requires cholesterol-rich domains.

Authors:  Sarah Frankland; Akinola Adisa; Paul Horrocks; Theodore F Taraschi; Timothy Schneider; Salenna R Elliott; Stephen J Rogerson; Ellen Knuepfer; Alan F Cowman; Chris I Newbold; Leann Tilley
Journal:  Eukaryot Cell       Date:  2006-05

3.  Control of erythrocyte membrane-skeletal cohesion by the spectrin-membrane linkage.

Authors:  Lionel Blanc; Marcela Salomao; Xinhua Guo; Xiuli An; Walter Gratzer; Narla Mohandas
Journal:  Biochemistry       Date:  2010-06-01       Impact factor: 3.162

4.  ATP/ADP binding to a novel nucleotide binding domain of the reticulocyte-binding protein Py235 of Plasmodium yoelii.

Authors:  Jeya Kumar Ramalingam; Cornelia Hunke; Xiaohong Gao; Gerhard Grüber; Peter Rainer Preiser
Journal:  J Biol Chem       Date:  2008-10-28       Impact factor: 5.157

5.  Structural determination of functional units of the nucleotide binding domain (NBD94) of the reticulocyte binding protein Py235 of Plasmodium yoelii.

Authors:  Ardina Grüber; Malathy S S Manimekalai; Asha M Balakrishna; Cornelia Hunke; Jeyaraman Jeyakanthan; Peter R Preiser; Gerhard Grüber
Journal:  PLoS One       Date:  2010-02-10       Impact factor: 3.240

6.  Erythrocytes carrying mutations in spectrin and protein 4.1 show differing sensitivities to invasion by Plasmodium falciparum.

Authors:  C A Facer
Journal:  Parasitol Res       Date:  1995       Impact factor: 2.289

  6 in total

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