Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

miR-181a-regulated pathways in T-cell differentiation and aging

Full metadata record
DC Field Value Language
dc.contributor.authorKim, Chulwoo-
dc.contributor.authorYe, Zhongde-
dc.contributor.authorWeyand, Cornelia M.-
dc.contributor.authorGoronzy, Jorg J.-
dc.date.accessioned2022-02-28T21:42:40Z-
dc.date.available2022-02-28T21:42:40Z-
dc.date.created2021-12-07-
dc.date.issued2021-06-15-
dc.identifier.issn1742-4933-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/137301-
dc.description.abstractMicroRNAs (miRNAs) are regulatory noncoding RNAs important for many aspects of cellular processes including cell differentiation and proliferation. Functions of numerous miRNAs have been identified in T cells, with miR-181a regulating T cell activation thresholds during thymic T cell development and during activation of peripheral T cells. Intriguingly, miR-181a is implicated in defective antiviral and vaccine responses in older individuals, as its expression declines in naive T cells with increasing age. Here, we review the pathways that are regulated by miR-181a and that explain the unique role of miR-181a in T cell development, T cell activation and antiviral T cell responses. These studies provide a framework for understanding how a decline in miR-181a expression in T cells could contribute to age-related defects in adaptive immunity. We furthermore review the mechanisms that cause the age-related decline in miR-181a expression and discuss the potential of restoring miR-181a expression or targeting miR-181a-regulated pathways to improve impaired T cell responses in older individuals.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherBMC-
dc.subjectDOSE INFLUENZA VACCINE-
dc.subjectMIR-181A EXPRESSION-
dc.subjectDOUBLE-BLIND-
dc.subjectLIFE-SPAN-
dc.subjectACTIVATION-
dc.subjectTRANSCRIPTION-
dc.subjectRESPONSES-
dc.subjectSELECTION-
dc.subjectEFFECTOR-
dc.subjectAGE-
dc.titlemiR-181a-regulated pathways in T-cell differentiation and aging-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Chulwoo-
dc.identifier.doi10.1186/s12979-021-00240-1-
dc.identifier.scopusid2-s2.0-85107972953-
dc.identifier.wosid000661895100001-
dc.identifier.bibliographicCitationIMMUNITY & AGEING, v.18, no.1-
dc.relation.isPartOfIMMUNITY & AGEING-
dc.citation.titleIMMUNITY & AGEING-
dc.citation.volume18-
dc.citation.number1-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGeriatrics & Gerontology-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryGeriatrics & Gerontology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusAGE-
dc.subject.keywordPlusDOSE INFLUENZA VACCINE-
dc.subject.keywordPlusDOUBLE-BLIND-
dc.subject.keywordPlusEFFECTOR-
dc.subject.keywordPlusLIFE-SPAN-
dc.subject.keywordPlusMIR-181A EXPRESSION-
dc.subject.keywordPlusRESPONSES-
dc.subject.keywordPlusSELECTION-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordAuthorInfectious disease-
dc.subject.keywordAuthorMemory T cells-
dc.subject.keywordAuthorReplication stress-
dc.subject.keywordAuthorT cell activation-
dc.subject.keywordAuthorT cell aging-
dc.subject.keywordAuthorT cell differentiation-
dc.subject.keywordAuthorVaccine-
dc.subject.keywordAuthormiR-181a-
dc.subject.keywordAuthormicroRNA-
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Medicine > Department of Medical Science > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE