Activation of mitogen-activated protein kinases and AP-1 by polysaccharide isolated from the radix of Platycodon grandiflorum in RAW 264.7 cells

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dc.contributor.authorYeo Dae Yoon-
dc.contributor.authorJong Soon Kang-
dc.contributor.authorSang Bae Han-
dc.contributor.authorSong Kyu Park-
dc.contributor.authorHyun Sun Lee-
dc.contributor.authorJ S Kang-
dc.contributor.authorHwan Mook Kim-
dc.date.accessioned2017-04-19T09:01:27Z-
dc.date.available2017-04-19T09:01:27Z-
dc.date.issued2004-
dc.identifier.issn1567-5769-
dc.identifier.uri10.1016/j.intimp.2004.06.012ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/6627-
dc.description.abstractThe root of Platycodon grandiflorum has been widely used for the treatment of various diseases in oriental medicine. Our previous study showed that the PG, a polysaccharide isolated from P. grandiflorum, activates macrophages via Toll-like receptor 4 (TLR4). However, the associated biological mechanisms are not fully understood. To elucidate the molecular mechanism responsible for the macrophage activation, we investigated the effect of PG on the activity of mitogen-activated protein kinases (MAPKs) and activator protein-1 (AP-1) in RAW 264.7 cells, a murine macrophage cell line. Treatment of RAW 264.7 cells with PG produced a marked induction of AP-1 DNA binding activity. Moreover, all three MAPKs were activated by PG, and PG-induced activation of MAPKs was abrogated by the treatment of PD98059, curcumin, and SB203580, specific inhibitors of MEK-1/2, stress-activated protein kinases/jun N-terminal kinase (SAPK/JNK), and p38 MAP kianse, respectively. The induction of AP-1 DNA binding activity by PG was also inhibited by these MAPK inhibitors. Moreover, supershift analysis identified that JunB and Fra-1 are major components involved in the PG-mediated induction of AP-1 DNA binding. Additionally, curcumin and SB203580 suppressed PG-induced production of nitric oxide (NO) and tumor necrosis factor-α (TNF-α), whereas PD98059 showed an inhibitory effect only on the TNF-α production. Taken together, these results suggest that macrophage activation by PG is mediated, at least in part, by MAPKs and AP-1.-
dc.publisherElsevier-
dc.titleActivation of mitogen-activated protein kinases and AP-1 by polysaccharide isolated from the radix of Platycodon grandiflorum in RAW 264.7 cells-
dc.title.alternativeActivation of mitogen-activated protein kinases and AP-1 by polysaccharide isolated from the radix of Platycodon grandiflorum in RAW 264.7 cells-
dc.typeArticle-
dc.citation.titleInternational Immunopharmacology-
dc.citation.number12-
dc.citation.endPage1487-
dc.citation.startPage1477-
dc.citation.volume4-
dc.contributor.affiliatedAuthorYeo Dae Yoon-
dc.contributor.affiliatedAuthorJong Soon Kang-
dc.contributor.affiliatedAuthorSang Bae Han-
dc.contributor.affiliatedAuthorSong Kyu Park-
dc.contributor.affiliatedAuthorHyun Sun Lee-
dc.contributor.affiliatedAuthorHwan Mook Kim-
dc.contributor.alternativeName윤여대-
dc.contributor.alternativeName강종순-
dc.contributor.alternativeName한상배-
dc.contributor.alternativeName박성규-
dc.contributor.alternativeName이현선-
dc.contributor.alternativeName강종성-
dc.contributor.alternativeName김환묵-
dc.identifier.bibliographicCitationInternational Immunopharmacology, vol. 4, no. 12, pp. 1477-1487-
dc.identifier.doi10.1016/j.intimp.2004.06.012-
dc.subject.keywordAP-1-
dc.subject.keywordMacrophage-
dc.subject.keywordMAPK-
dc.subject.keywordPlatycodon grandiflorum-
dc.subject.localAP-1-
dc.subject.localmacrophage-
dc.subject.localmacrophages-
dc.subject.localMacrophage-
dc.subject.localMacrophages-
dc.subject.localMAPK-
dc.subject.localMAPKs-
dc.subject.localPlatycodon grandiflorum-
dc.subject.localPLATYCODON GRANDIFLORUM-
dc.subject.localplatycodon grandiflorum-
dc.description.journalClassY-
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Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
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