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The herbal-derived honokiol and magnolol enhances immune response to infection with methicillin-sensitive Staphylococcus aureus (MSSA) and methicillin-resistant S-aureus (MRSA)

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dc.contributor.authorChoi, Eun-Jin-
dc.contributor.authorKim, Hyung-Ip-
dc.contributor.authorKim, Ji-Ae-
dc.contributor.authorJun, Soo Youn-
dc.contributor.authorKang, Sang Hyeon-
dc.contributor.authorPark, Dong June-
dc.contributor.authorSon, Seok-Jun-
dc.contributor.authorKim, Younghoon-
dc.contributor.authorShin, Ok Sarah-
dc.date.accessioned2021-09-04T16:51:42Z-
dc.date.available2021-09-04T16:51:42Z-
dc.date.created2021-06-18-
dc.date.issued2015-05-
dc.identifier.issn0175-7598-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/93765-
dc.description.abstractThe emergence of antibiotic resistant strains such as methicillin-resistant Staphylococcus aureus (MRSA) reminds us an urgent need to develop a new immune-modulating agent for preventing S. aureus infection. In this study, we found that herbal medicines, honokiol and magnolol, caused a significant cellular immune modulatory effect during S. aureus infection. In mouse macrophages, these compounds drove upregulation of an antioxidant effect in response to S. aureus, resulting in a dampened total cellular reactive oxygen species (ROS) production and decreased production of inflammatory cytokines/chemokines, whereas honokiol induced increased types I and III interferon messenger RNA (mRNA) expression levels in response to MSSA infection. Moreover, the internalization of S. aureus by human alveolar epithelial cells was inhibited by these compounds. Furthermore, honokiol and magnolol treatment promoted a delay in killing during MSSA infection in Caenorhabditis elegans, suggesting antimicrobial function in vivo. In conclusion, honokiol and magnolol may be considered as attractive immune-modulating treatment for S. aureus infection.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherSPRINGER-
dc.subjectALVEOLAR EPITHELIAL-CELLS-
dc.subjectCAENORHABDITIS-ELEGANS-
dc.subjectANTIMICROBIAL ACTIVITY-
dc.subjectENDOTHELIAL-CELLS-
dc.subjectSIGNALING PATHWAY-
dc.subjectBIOFILM FORMATION-
dc.subjectNATURAL-PRODUCT-
dc.subjectALPHA-TOXIN-
dc.subjectRAT MODEL-
dc.subjectIN-VITRO-
dc.titleThe herbal-derived honokiol and magnolol enhances immune response to infection with methicillin-sensitive Staphylococcus aureus (MSSA) and methicillin-resistant S-aureus (MRSA)-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Ok Sarah-
dc.identifier.doi10.1007/s00253-015-6382-y-
dc.identifier.scopusid2-s2.0-84939968191-
dc.identifier.wosid000353826200022-
dc.identifier.bibliographicCitationAPPLIED MICROBIOLOGY AND BIOTECHNOLOGY, v.99, no.10, pp.4387 - 4396-
dc.relation.isPartOfAPPLIED MICROBIOLOGY AND BIOTECHNOLOGY-
dc.citation.titleAPPLIED MICROBIOLOGY AND BIOTECHNOLOGY-
dc.citation.volume99-
dc.citation.number10-
dc.citation.startPage4387-
dc.citation.endPage4396-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusALVEOLAR EPITHELIAL-CELLS-
dc.subject.keywordPlusCAENORHABDITIS-ELEGANS-
dc.subject.keywordPlusANTIMICROBIAL ACTIVITY-
dc.subject.keywordPlusENDOTHELIAL-CELLS-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusBIOFILM FORMATION-
dc.subject.keywordPlusNATURAL-PRODUCT-
dc.subject.keywordPlusALPHA-TOXIN-
dc.subject.keywordPlusRAT MODEL-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordAuthorS. aureus-
dc.subject.keywordAuthorHerbal medicine-
dc.subject.keywordAuthorImmune-modulating activity-
dc.subject.keywordAuthorC. elegans-
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