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dc.contributor.author김길현-
dc.date.accessioned2018-12-27T16:30:06Z-
dc.date.available2018-12-27T16:30:06Z-
dc.date.issued1997-
dc.identifier.issn1225-8687-
dc.identifier.otherOAK-17035-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/247966-
dc.description.abstractMany cell types are known to stimulate CD8+ T cells in allogeneic recognition such as mixed lymphocyte reaction (MLR). Whereas dendritic cells are most potent among them, T cells are usually considered very poor in stimulating CD8+ T cells although there are some tumor cells that are weakly stimulatory. T cells, as a stimulator, cultured in the presence of concanavalin A that were otherwise nonstimulatory to CD8+ T cells appeared to stimulate CD8+ T cells strongly when they were pretreated with neuraminidase. The enhancement of MLR by neuraminidase could be achieved by treating either the stimulators or responders with neuraminidase. Removal of negatively-charged sialic acid moieties from the cell surface, which reduced electrostatic repulsion between responders and stimulators to give better cell-cell contact might be responsible for the enhanced MLR. In addition, neuraminidase treatment also appeared to deliver activation signal to responding T cells since it could activate CD8+ T cells in synergy with phorbol myristate acetate. The maximal responses were observed when both responders and stimulators were treated with neuraminidase.-
dc.languageEnglish-
dc.titleNeuraminidase treatment enhances allogeneic stimulation of unprimed CD8+ T cells-
dc.typeArticle-
dc.relation.issue6-
dc.relation.volume30-
dc.relation.indexSCOPUS-
dc.relation.startpage385-
dc.relation.lastpage389-
dc.relation.journaltitleJournal of Biochemistry and Molecular Biology-
dc.identifier.scopusid2-s2.0-0031328387-
dc.author.googleKim K.-
dc.contributor.scopusid김길현(56092131700)-
dc.date.modifydate20211210152111-
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자연과학대학 > 생명과학전공 > Journal papers
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