DC Field | Value | Language |
---|---|---|
dc.contributor.author | Y H Ban | - |
dc.contributor.author | Se-Chan Oh | - |
dc.contributor.author | Sang-Hwan Seo | - |
dc.contributor.author | Seok-Min Kim | - |
dc.contributor.author | In Pyo Choi | - |
dc.contributor.author | P D Greenberg | - |
dc.contributor.author | J Chang | - |
dc.contributor.author | Tae-Don Kim | - |
dc.contributor.author | S J Ha | - |
dc.date.accessioned | 2018-01-11 | - |
dc.date.available | 2018-01-11 | - |
dc.date.issued | 2017 | - |
dc.identifier.issn | 2211-1247 | - |
dc.identifier.uri | 10.1016/j.celrep.2017.08.065 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/17435 | - |
dc.description.abstract | MicroRNA (miR)-150 is a developmental regulator of several immune-cell types, but its role in CD8+ T cells is largely unexplored. Here, we show that miR-150 regulates the generation of memory CD8+ T cells. After acute virus infection, miR-150 knockout (KO) mice exhibited an accelerated differentiation of CD8+ T cells into memory cells and improved production of effector cytokines. Additionally, miR-150 KO CD8+ T cells displayed an enhanced recall response and improved protection against infections with another virus and bacteria. We found that forkhead box O1 (Foxo1) and T cell-specific transcription factor 1 (TCF1) are upregulated during the early activation phase in miR-150 KO CD8+ T cells and that miR-150 directly targets and suppresses Foxo1. These results suggest that miR-150-mediated suppression of Foxo1 regulates the balance between effector and memory cell differentiation, which might aid in the development of improved vaccines and T cell therapeutics | - |
dc.publisher | Elsevier-Cell Press | - |
dc.title | miR-150-mediated Foxo1 regulation programs CD8+ T cell differentiation | - |
dc.title.alternative | miR-150-mediated Foxo1 regulation programs CD8+ T cell differentiation | - |
dc.type | Article | - |
dc.citation.title | Cell Reports | - |
dc.citation.number | 11 | - |
dc.citation.endPage | 2611 | - |
dc.citation.startPage | 2598 | - |
dc.citation.volume | 20 | - |
dc.contributor.affiliatedAuthor | Se-Chan Oh | - |
dc.contributor.affiliatedAuthor | Sang-Hwan Seo | - |
dc.contributor.affiliatedAuthor | Seok-Min Kim | - |
dc.contributor.affiliatedAuthor | In Pyo Choi | - |
dc.contributor.affiliatedAuthor | Tae-Don Kim | - |
dc.contributor.alternativeName | 반영호 | - |
dc.contributor.alternativeName | 오세찬 | - |
dc.contributor.alternativeName | 서상환 | - |
dc.contributor.alternativeName | 김석민 | - |
dc.contributor.alternativeName | 최인표 | - |
dc.contributor.alternativeName | Greenberg | - |
dc.contributor.alternativeName | 창준 | - |
dc.contributor.alternativeName | 김태돈 | - |
dc.contributor.alternativeName | 하상준 | - |
dc.identifier.bibliographicCitation | Cell Reports, vol. 20, no. 11, pp. 2598-2611 | - |
dc.identifier.doi | 10.1016/j.celrep.2017.08.065 | - |
dc.subject.keyword | acute | - |
dc.subject.keyword | CD8 | - |
dc.subject.keyword | differentiation | - |
dc.subject.keyword | Foxo1 | - |
dc.subject.keyword | infection | - |
dc.subject.keyword | LCMV | - |
dc.subject.keyword | memory | - |
dc.subject.keyword | miR-150 | - |
dc.subject.keyword | primary immune response | - |
dc.subject.keyword | recall | - |
dc.subject.local | acute | - |
dc.subject.local | Acute | - |
dc.subject.local | CD8 | - |
dc.subject.local | differentiation | - |
dc.subject.local | Differentiation | - |
dc.subject.local | Foxo1 | - |
dc.subject.local | FoxO1 | - |
dc.subject.local | Infection | - |
dc.subject.local | infection | - |
dc.subject.local | LCMV | - |
dc.subject.local | memory | - |
dc.subject.local | Memory | - |
dc.subject.local | MiR-150 | - |
dc.subject.local | miR-150 | - |
dc.subject.local | primary immune response | - |
dc.subject.local | recall | - |
dc.description.journalClass | Y | - |
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