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NRF2 activation by 2-methoxycinnamaldehyde attenuates inflammatory responses in macrophages via enhancing autophagy flux

DC Field Value Language
dc.contributor.authorKim, Bo-Sung-
dc.contributor.authorShin, Minwook-
dc.contributor.authorKim, Kyu-Won-
dc.contributor.authorHa, Ki-Tae-
dc.contributor.authorBae, Sung-Jin-
dc.date.accessioned2022-10-17T04:47:16Z-
dc.date.available2022-10-17T04:47:16Z-
dc.date.created2022-10-13-
dc.date.issued2022-08-
dc.identifier.citationBMB Reports, Vol.55 No.8, pp.407-412-
dc.identifier.issn1976-6696-
dc.identifier.urihttps://hdl.handle.net/10371/186381-
dc.description.abstractA well-controlled inflammatory response is crucial for the recovery from injury and maintenance of tissue homeostasis. The anti-inflammatory response of 2-methoxycinnamaldehyde (2-MCA), a natural compound derived from cinnamon, has been studied; however, the underlying mechanism on macrophage has not been fully elucidated. In this study, LPS-stimulated production of TNF-alpha and NO was reduced by 2-MCA in macrophages. 2-MCA significantly activated the NRF2 pathway, and expression levels of autophagy-associated proteins in macrophages, including LC3 and P62, were enhanced via NRF2 activation regard-less of LPS treatment, suggesting the occurrence of 2-MCA -mediated autophagy. Moreover, evaluation of autophagy flux using luciferase-conjugated LC3 revealed that incremental LC3 and P62 levels are coupled to enhanced autophagy flux. Finally, reduced expression levels of TNF-alpha and NOS2 by 2-MCA were reversed by autophagy inhibitors, such as bafilomycin A1 and NH4Cl, in LPS-stimulated macrophages. In conclusion, 2-MCA enhances autophagy flux in macrophages via NRF2 activation and consequently reduces LPS-induced inflammation.-
dc.language영어-
dc.publisher생화학분자생물학회-
dc.titleNRF2 activation by 2-methoxycinnamaldehyde attenuates inflammatory responses in macrophages via enhancing autophagy flux-
dc.typeArticle-
dc.identifier.doi10.5483/BMBRep.2022.55.8.065-
dc.citation.journaltitleBMB Reports-
dc.identifier.wosid000861372500007-
dc.identifier.scopusid2-s2.0-85137134997-
dc.citation.endpage412-
dc.citation.number8-
dc.citation.startpage407-
dc.citation.volume55-
dc.identifier.kciidART002870437-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorKim, Kyu-Won-
dc.type.docTypeArticle-
dc.description.journalClass1-
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