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dc.contributor.authorBokori-Brown, M
dc.contributor.authorPetrov, PG
dc.contributor.authorKhafaji, MA
dc.contributor.authorMughal, MK
dc.contributor.authorNaylor, CE
dc.contributor.authorShore, AC
dc.contributor.authorGooding, KM
dc.contributor.authorCasanova, F
dc.contributor.authorMitchell, TJ
dc.contributor.authorTitball, RW
dc.contributor.authorWinlove, CP
dc.date.accessioned2016-04-07T09:28:42Z
dc.date.issued2016-03-16
dc.description.abstractThis study investigated the effect of the biochemical and biophysical properties of the plasma membrane as well as membrane morphology on the susceptibility of human red blood cells to the cholesterol-dependent cytolysin pneumolysin, a key virulence factor of Streptococcus pneumoniae, using single cell studies. We show a correlation between the physical properties of the membrane (bending rigidity, surface and dipole electrostatic potentials) and the susceptibility of red blood cells to pneumolysin-induced haemolysis. We demonstrate that biochemical modifications of the membrane induced by oxidative stress, lipid scrambling and artificial cell aging modulate the cell response to the toxin. We provide evidence that the diversity of response to pneumolysin in diabetic red blood cells correlates with levels of glycated haemoglobin (Hba1c) and that the mechanical properties of the red blood cell plasma membrane are altered in diabetes. Finally, we show that diabetic red blood cells are more resistant to pneumolysin and the related toxin perfringolysin O relative to healthy red blood cells. Taken together, these studies indicate that the diversity of cell response to pneumolysin within a population of human red blood cells is influenced by the biophysical and biochemical status of the plasma membrane and the chemical and/or oxidative stress prehistory of the cell.en_GB
dc.description.sponsorshipThe work was supported by the National Institute for Health Research (NIHR) Exeter Clinical Research Facility. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health. We also thank E. Green, S. A. Jewell, P. Gologan, M. J. Smallwood and R. Tennant for their help with the experimental techniques.en_GB
dc.identifier.citationFirst published online on March 16, 2016en_GB
dc.identifier.doi10.1074/jbc.M115.691899
dc.identifier.otherM115.691899
dc.identifier.urihttp://hdl.handle.net/10871/21005
dc.language.isoenen_GB
dc.publisherAmerican Society for Biochemistry and Molecular Biologyen_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/26984406en_GB
dc.rightsCopyright © 2016, The American Society for Biochemistry and Molecular Biology. This is the author accepted manuscript. The final version is available from American Society for Biochemistry and Molecular Biology via the DOI in this record.en_GB
dc.subjectagingen_GB
dc.subjectbacterial toxinen_GB
dc.subjectbending rigidityen_GB
dc.subjectdiabetesen_GB
dc.subjectdipole potentialen_GB
dc.subjecterythrocyteen_GB
dc.subjectmembrane biophysicsen_GB
dc.subjectoxidative stressen_GB
dc.subjectpneumolysinen_GB
dc.subjectsurface potentialen_GB
dc.titleRed Blood Cell Susceptibility to Pneumolysin: Correlation with Membrane Biochemical and Physical Properties.en_GB
dc.typeArticleen_GB
dc.date.available2016-04-07T09:28:42Z
dc.identifier.issn0021-9258
dc.descriptionPublished onlineen_GB
dc.identifier.eissn1083-351X
dc.identifier.journalJournal of Biological Chemistryen_GB


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