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dc.contributor.author오세관*
dc.date.accessioned2016-08-28T11:08:02Z-
dc.date.available2016-08-28T11:08:02Z-
dc.date.issued2008*
dc.identifier.issn1976-9148*
dc.identifier.otherOAK-13272*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/229291-
dc.description.abstractApoptosis is essential for a variety of pathophysiological progress. Apoptosis induction by various agents changes cellular morphology, DNA content and lipid membrane composition. Recently, sphingosine 1-phosphate (S1P) is avidly released from not only platelets and erythrocytes but vascular endothelium. Here we established S1P releasing cells by deleting S1P lyase (F9-12 cells). We observed apoptosis induction by the treatment of fumonisin B1 (FB1) in F9-12 cells but not in F9 wild-type cells. We measured high amounts of accumulated S1P and dihydroS1P (DHS1P) in FB1-induced apoptotic F9-12 cells. We also showed DHS1P release in an early stage of the apoptosis induction by FB1 but not by phorbol 12-myristate 13-acetate (PMA)-induced apoptosis, suggesting differential apoptotic processes.*
dc.languageEnglish*
dc.titleFumonisin B1 induces apoptosis in sphingosine 1-phosphate lyase-null F9 cells through increase of sphingolipids levels*
dc.typeArticle*
dc.relation.issue2*
dc.relation.volume16*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage95*
dc.relation.lastpage99*
dc.relation.journaltitleBiomolecules and Therapeutics*
dc.identifier.doi10.4062/biomolther.2008.16.2.095*
dc.identifier.wosidWOS:000257695700005*
dc.identifier.scopusid2-s2.0-69549116568*
dc.author.googlePak S.-M.*
dc.author.googlePark N.-Y.*
dc.author.googlePark M.-Y.*
dc.author.googleKim W.-J.*
dc.author.googleLee J.-H.*
dc.author.googleOh S.*
dc.author.googleYoo H.-S.*
dc.author.googleLee Y.-M.*
dc.contributor.scopusid오세관(7404103757)*
dc.date.modifydate20240118133340*
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의과대학 > 의학과 > Journal papers
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