Endotoxin contamination in commercially available pokeweed mitogen contributes to the activation of murine macrophages and human dendritic cell maturation

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dc.contributor.authorYang, Jae Seungko
dc.contributor.authorKim, Hye Jinko
dc.contributor.authorRyu, Young Heeko
dc.contributor.authorYun, Cheol-Heuiko
dc.contributor.authorChung, Dae Kyunko
dc.contributor.authorHan, Seung Hyunko
dc.date.accessioned2013-03-06T15:08:48Z-
dc.date.available2013-03-06T15:08:48Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2006-
dc.identifier.citationJOURNAL OF IMMUNOLOGY, v.176, pp.S35 - S35-
dc.identifier.issn0022-1767-
dc.identifier.urihttp://hdl.handle.net/10203/87364-
dc.description.abstractCommercially available pokeweed mitogen (PWM) has been reported to activate macrophages, leading to production of proinflammatory cytokines and nitric oxide (NO). However, we found that polymyxin B (PMB), a specific inhibitor of endotoxin activity, inhibited the PWM-induced expression of proinflammatory cytokines and NO and the activation of Toll-like receptor 4 (TLR4). A kinetic-turbidimetric Limulus amebocyte lysate assay demonstrated that commercial PWM contained substantial endotoxin, over 104 endotoxin units/mg of the PWM. A PWM re purified by PMB-coupled beads no longer induced the expression of proinflammatory cytokines, TLR4 activation, or dendritic cell maturation. However, the repurified PWM remained able to induce proliferation of human lymphocytes, which is a representative characteristic of PWM. These results suggest that commercial PWM might be contaminated with a large amount of endotoxin, resulting in the attribution of misleading immunological properties to PWM.-
dc.languageEnglish-
dc.publisherAMER ASSOC IMMUNOLOGISTS-
dc.titleEndotoxin contamination in commercially available pokeweed mitogen contributes to the activation of murine macrophages and human dendritic cell maturation-
dc.typeArticle-
dc.identifier.scopusid2-s2.0-33645537080-
dc.type.rimsART-
dc.citation.volume176-
dc.citation.beginningpageS35-
dc.citation.endingpageS35-
dc.citation.publicationnameJOURNAL OF IMMUNOLOGY-
dc.identifier.doi10.1128/CVI.13.3.309-313.2006-
dc.contributor.localauthorYang, Jae Seung-
dc.contributor.nonIdAuthorKim, Hye Jin-
dc.contributor.nonIdAuthorRyu, Young Hee-
dc.contributor.nonIdAuthorYun, Cheol-Heui-
dc.contributor.nonIdAuthorChung, Dae Kyun-
dc.contributor.nonIdAuthorHan, Seung Hyun-
dc.description.isOpenAccessN-
dc.type.journalArticleMeeting Abstract-
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