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Binding of annexin V to oxidized lipid on oxidatively damaged erythrocyte

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dc.contributor.author이경은-
dc.contributor.author이경헌-
dc.contributor.author최여진-
dc.contributor.author이광호-
dc.contributor.author최수희-
dc.contributor.author이성호-
dc.contributor.author김학진-
dc.contributor.author이광제-
dc.contributor.author김태호-
dc.contributor.author고홍숙-
dc.contributor.author김치정-
dc.contributor.author류왕성-
dc.date.available2019-06-10T07:30:32Z-
dc.date.issued2006-04-
dc.identifier.issn1738-5520-
dc.identifier.issn1738-5555-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/25539-
dc.description.abstractBackground and Objectives: Annexin V is known to bind to the phosphatidylserine (PS) of damaged cell membranes. We recently demonstrated that annexin V binds to oxidized red blood cells (oxRBC). The aim of this study was to find whether annexin V binds to oxidized lipids or to the PS of oxRBC. Materials and Methods: Red blood cells (RBC) were oxidized by the addition of CuSO4, and the degree of oxidation evaluated using the semiquantitative measurement of thiobarbituric acid reactive substance (TBARS). The binding of annexin V to oxRBC was evaluated by flow cytometry. Results: Annexin V was found to bind to oxRBC, but not to native RBC. The percentage of RBC binding to annexin V was closely correlated with the degree of oxidation, as measured using TBARS (r=0.99, p=0.000) in relation to the concentration of CuSO4. The binding of annexin V to oxRBC was attenuated in the presence of oxidized low density lipoprotein (oxLDL), with these phenomena also being dose-dependent. The binding was reduced by 71.0±3.0% in the presence of 100 μg/mL oxLDL. LDL had no influence on the binding of annexin V to oxRBC. Conclusion: These findings suggest that annexin V may bind to the oxidized lipids of cell membranes. Further studies will be required to evaluate the relative importance between oxidized lipids and PS, and to find the characteristics of oxidized lipids in the binding of annexin V to damaged cell membranes. © 2006, The Korean Society of Circulation.-
dc.format.extent7-
dc.language한국어-
dc.language.isoKOR-
dc.publisherKorean Society of Circulation-
dc.titleBinding of annexin V to oxidized lipid on oxidatively damaged erythrocyte-
dc.typeArticle-
dc.identifier.doi10.4070/kcj.2006.36.4.285-
dc.identifier.bibliographicCitationKorean Circulation Journal, v.36, no.4, pp 285 - 291-
dc.identifier.kciidART001137109-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-33646480814-
dc.citation.endPage291-
dc.citation.number4-
dc.citation.startPage285-
dc.citation.titleKorean Circulation Journal-
dc.citation.volume36-
dc.type.docTypeArticle-
dc.publisher.location대한민국-
dc.subject.keywordAuthorAnnexin V-
dc.subject.keywordAuthorBinding-
dc.subject.keywordAuthorErythrocytes-
dc.subject.keywordAuthorLipid peroxidation-
dc.subject.keywordAuthorLow density lipoprotein-
dc.subject.keywordPluscopper sulfate-
dc.subject.keywordPluslipocortin 5-
dc.subject.keywordPluslow density lipoprotein-
dc.subject.keywordPlusthiobarbituric acid reactive substance-
dc.subject.keywordPlusarticle-
dc.subject.keywordPluscell damage-
dc.subject.keywordPluserythrocyte-
dc.subject.keywordPlusflow cytometry-
dc.subject.keywordPluslipid peroxidation-
dc.subject.keywordPlusoxidation-
dc.subject.keywordPlusprotein binding-
dc.subject.keywordPlusprotein lipid interaction-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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