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The Effect of miR-146a on the Gene Expression of Immunoregulatory Cytokines in Human Mesenchymal Stromal Cells

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dc.contributor.authorKo, Jung Hwa-
dc.contributor.authorOh, Joo Youn-
dc.date.accessioned2023-04-28T06:56:45Z-
dc.date.available2023-04-28T06:56:45Z-
dc.date.created2020-11-10-
dc.date.created2020-11-10-
dc.date.created2020-11-10-
dc.date.created2020-11-10-
dc.date.issued2020-09-
dc.identifier.citationInternational Journal of Molecular Sciences, Vol.21 No.18, pp.6809-9-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://hdl.handle.net/10371/191714-
dc.description.abstractMounting evidence indicates that microRNAs (miRNAs), including miR-146a, have an impact on the immunomodulatory activities of mesenchymal stem/stromal cells (MSCs). Suppression of inflammatory macrophage activation is one of the main immunomodulatory mechanisms of MSCs. Here, we investigated whether miR-146a in MSCs might play a role in the effects of MSCs on macrophage activation. A miRNA microarray revealed that miR-146a was the most highly upregulated miRNA in MSCs upon co-culture with activated macrophages. Inhibition of miR-146a in MSCs through miR-146a inhibitor transfection had a different effect on the expression of immunoregulatory factors secreted by MSCs. Pentraxin 3, tumor necrosis factor-inducible gene 6, and cyclooxygenase-2, which are well-known mediators of the immunomodulatory functions of MSCs, were significantly upregulated in MSCs after miR-146a knockdown. By contrast, hepatocyte growth factor and stanniocalcin 1, other immunoregulatory molecules expressed by MSCs, were downregulated by miR-146a knockdown. Consequently, the inhibition of miR-146a in MSCs did not change the overall effect of MSCs on the suppression of inflammatory macrophage activation or the induction of anti-inflammatory macrophage polarization.-
dc.language영어-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleThe Effect of miR-146a on the Gene Expression of Immunoregulatory Cytokines in Human Mesenchymal Stromal Cells-
dc.typeArticle-
dc.identifier.doi10.3390/ijms21186809-
dc.citation.journaltitleInternational Journal of Molecular Sciences-
dc.identifier.wosid000581663900001-
dc.identifier.scopusid2-s2.0-85090906397-
dc.citation.endpage9-
dc.citation.number18-
dc.citation.startpage6809-
dc.citation.volume21-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorOh, Joo Youn-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusTISSUE-
dc.subject.keywordPlusMSCS-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusSECRETE-
dc.subject.keywordAuthorimmunoregulatory factor-
dc.subject.keywordAuthormacrophage-
dc.subject.keywordAuthormesenchymal stem-
dc.subject.keywordAuthorstromal cell-
dc.subject.keywordAuthormicroRNA-
dc.subject.keywordAuthormiR-146a-
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  • College of Medicine
  • Department of Medicine
Research Area 각막 및 외안부 질환, 백내장

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