Chrysin derivative CM1 and exhibited anti-inflammatory action by upregulating toll-iInteracting protein expression in lipopolysaccharide-stimulated RAW264.7 macrophage cells

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dc.contributor.authorE B Byun-
dc.contributor.authorH Y Song-
dc.contributor.authorWoo Sik Kim-
dc.contributor.authorJ M Han-
dc.contributor.authorH S Seo-
dc.contributor.authorW Y Park-
dc.contributor.authorK Kim-
dc.contributor.authorE H Byun-
dc.date.accessioned2021-04-06T03:31:03Z-
dc.date.available2021-04-06T03:31:03Z-
dc.date.issued2021-
dc.identifier.issn1420-3049-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/24242-
dc.description.abstractAlthough our previous study revealed that gamma-irradiated chrysin enhanced anti-inflammatory activity compared to intact chrysin, it remains unclear whether the chrysin derivative, CM1, produced by gamma irradiation, negatively regulates toll-like receptor (TLR) signaling. In this study, we investigated the molecular basis for the downregulation of TLR4 signal transduction by CM1 in macrophages. We initially determined the appropriate concentration of CM1 and found no cellular toxicity below 2 μg/mL. Upon stimulation with lipopolysaccharide (LPS), CM1 modulated LPS-stimulated inflammatory action by suppressing the release of proinflammatory mediators (cytokines TNF-α and IL-6) and nitric oxide (NO) and downregulated the mitogen-activated protein kinase (MAPK) and nuclear factor-κB (NF-κB) signaling pathways. Furthermore, CM1 markedly elevated the expression of the TLR negative regulator toll-interacting protein (Tollip) in dose- and time-dependent manners. LPS-induced expression of cell surface molecules (CD80, CD86, and MHC class I/II), proinflammatory cytokines (TNF-α and IL-6), COX-2, and iNOS-mediated NO were inhibited by CM1; these effects were prevented by the knockdown of Tollip expression. Additionally, CM1 did not affect the downregulation of LPS-induced expression of MAPKs and NF-κB signaling in Tollip-downregulated cells. These findings provide insight into effective therapeutic intervention of inflammatory disease by increasing the understanding of the negative regulation of TLR signaling induced by CM1.-
dc.publisherMDPI-
dc.titleChrysin derivative CM1 and exhibited anti-inflammatory action by upregulating toll-iInteracting protein expression in lipopolysaccharide-stimulated RAW264.7 macrophage cells-
dc.title.alternativeChrysin derivative CM1 and exhibited anti-inflammatory action by upregulating toll-iInteracting protein expression in lipopolysaccharide-stimulated RAW264.7 macrophage cells-
dc.typeArticle-
dc.citation.titleMolecules-
dc.citation.number6-
dc.citation.endPage1532-
dc.citation.startPage1532-
dc.citation.volume26-
dc.contributor.affiliatedAuthorWoo Sik Kim-
dc.contributor.alternativeName변의백-
dc.contributor.alternativeName송하연-
dc.contributor.alternativeName김우식-
dc.contributor.alternativeName한정무-
dc.contributor.alternativeName서호성-
dc.contributor.alternativeName박우용-
dc.contributor.alternativeName김광욱-
dc.contributor.alternativeName변의홍-
dc.identifier.bibliographicCitationMolecules, vol. 26, no. 6, pp. 1532-1532-
dc.identifier.doi10.3390/molecules26061532-
dc.subject.keywordChrysin derivative-
dc.subject.keywordAnti-inflammatory activity-
dc.subject.keywordToll-like receptor negative regulator-
dc.subject.keywordToll-interacting protein-
dc.subject.keywordMacrophage-
dc.subject.localChrysin derivative-
dc.subject.localAnti-inflammatory activity-
dc.subject.localAnti-infl ammatory activity-
dc.subject.localanti-inflammatory activity-
dc.subject.localAnti-inflammatory activities-
dc.subject.localToll-like receptor negative regulator-
dc.subject.localToll-interacting protein-
dc.subject.localmacrophages-
dc.subject.localmacrophage-
dc.subject.localMacrophages-
dc.subject.localMacrophage-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
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