Src kinase-targeted anti-inflammatory activity of davallialactone from Inonotus xeranticus in lipopolysaccharide-activated RAW264.7 cells

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dc.contributor.authorY G Lee-
dc.contributor.authorW M Lee-
dc.contributor.authorJ Y Kim-
dc.contributor.authorJ Y Lee-
dc.contributor.authorIn Kyoung Lee-
dc.contributor.authorBong Sik Yun-
dc.contributor.authorM H Rhee-
dc.contributor.authorJ Y Cho-
dc.date.accessioned2017-04-19T09:10:58Z-
dc.date.available2017-04-19T09:10:58Z-
dc.date.issued2008-
dc.identifier.issn0007-1188-
dc.identifier.uri10.1038/bjp.2008.136ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8476-
dc.description.abstractBackground and purpose: Mushrooms are popular both as food and as a source of natural compounds of biopharmaceutical interest. Some mushroom-derived compounds such as β-glucan have been shown to be immunostimulatory; this study explores the anti-inflammatory properties of hispidin analogues derived from the mushroom, Inonotus xeranticus. We sought to identify the molecular mechanism of action of these hispidin analogues by determining their effects on lipopolysaccharide (LPS)-mediated inflammatory responses in a macrophage cell line. Experimental approach: The production of inflammatory mediators was determined by Griess assay, reverse transcription-PCR and ELISA. The inhibitory effect of davalliactone on LPS-induced activation of signalling cascades was assessed by western blotting, immunoprecipitation and direct kinase assay. Key results: In activated RAW264.7 cells, davallialactone strongly downregulated LPS-mediated inflammatory responses, including NO production, prostaglandin E2 release, expression of proinflammatory cytokine genes and cell surface expression of co-stimulatory molecules. Davallialactone treatment did not alter cell viability or morphology. Davallialactone was found to exert its anti-inflammatory effects by inhibiting a signalling cascade that activates nuclear factor kappa B via PI3K, Akt and IKK, but not mitogen-activated protein kinases. Treatment with davallialactone affected the phosphorylation of these signalling proteins, but not their level of expression. These inhibitory effects were not due to the interruption of toll-like receptor 4 binding to CD14. In particular, davallialactone strongly inhibited the LPS-induced phosphorylation and kinase activity of Src, implying that Src may be a potential pharmacological target of davallialactone. Conclusions and implications: Our data suggest that davallialactone, a small molecule found in edible mushrooms, has anti-inflammatory activity. Davallialactone can be developed as a pharmaceutically valuable anti-Src kinase agent.-
dc.publisherWiley-
dc.titleSrc kinase-targeted anti-inflammatory activity of davallialactone from Inonotus xeranticus in lipopolysaccharide-activated RAW264.7 cells-
dc.title.alternativeSrc kinase-targeted anti-inflammatory activity of davallialactone from Inonotus xeranticus in lipopolysaccharide-activated RAW264.7 cells-
dc.typeArticle-
dc.citation.titleBritish Journal of Pharmacology-
dc.citation.number4-
dc.citation.endPage863-
dc.citation.startPage852-
dc.citation.volume154-
dc.contributor.affiliatedAuthorIn Kyoung Lee-
dc.contributor.affiliatedAuthorBong Sik Yun-
dc.contributor.alternativeName-
dc.contributor.alternativeName-
dc.contributor.alternativeName-
dc.contributor.alternativeName-
dc.contributor.alternativeName이인경-
dc.contributor.alternativeName윤봉식-
dc.contributor.alternativeName-
dc.contributor.alternativeName-
dc.identifier.bibliographicCitationBritish Journal of Pharmacology, vol. 154, no. 4, pp. 852-863-
dc.identifier.doi10.1038/bjp.2008.136-
dc.subject.keywordanti-inflammatory effect-
dc.subject.keyworddavallialactone-
dc.subject.keywordinonotus xeranticus-
dc.subject.keywordlipopolysaccharide-
dc.subject.keywordNF-κB-
dc.subject.keywordSrc kinase-
dc.subject.localAnti-Inflammatory Effect-
dc.subject.localAnti-inflammatory effect-
dc.subject.localanti-inflammatory effect-
dc.subject.localAnti-inflammatory effects-
dc.subject.localDavallialactone-
dc.subject.localdavallialactone-
dc.subject.localinonotus xeranticus-
dc.subject.localInonotus xeranticus-
dc.subject.locallipopolysaccharide (LPS)-
dc.subject.localLipopolysaccharide-
dc.subject.locallipopolysaccharide-
dc.subject.localLipopolysaccharide (LPS)-
dc.subject.localLipopolysaccharides-
dc.subject.localNuclear factor-kappa B-
dc.subject.localnuclear factor κB-
dc.subject.localNf-κb-
dc.subject.localNF-kB-
dc.subject.localnuclear factor kappa B-
dc.subject.localNF-κB (nuclear factor kappa-B)-
dc.subject.localNF-kappaB-
dc.subject.localNuclear factor-κb-
dc.subject.localNF-κ B-
dc.subject.localNF-κB-
dc.subject.localNF-kappa B-
dc.subject.localNuclear factor κB (NF-κB)-
dc.subject.localNuclear factor κB-
dc.subject.localNFκB-
dc.subject.localNf-κB-
dc.subject.localNuclear factor-κB-
dc.subject.localnuclear factorκB-
dc.subject.localNuclear factor (NF)-κB-
dc.subject.localNuclear factor kappa B-
dc.subject.localnuclear factor-κB-
dc.subject.localNF-ΚB-
dc.subject.localNuclear factor-kappa B (NF-κB)-
dc.subject.localNuclear factor-kappaB-
dc.subject.localnuclear factor-kappaB-
dc.subject.localnuclear factor-kappaB (NF-κB)-
dc.subject.localNFkappaB-
dc.subject.localNuclear factor kappaB-
dc.subject.localSrc kinase-
dc.description.journalClassY-
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