Cutting Edge: MicroRNA-181 Promotes Human NK Cell Development by Regulating Notch Signaling

被引:152
作者
Cichocki, Frank [1 ]
Felices, Martin [1 ]
McCullar, Valarie [1 ]
Presnell, Steven R. [2 ]
Al-Attar, Ahmad [2 ]
Lutz, Charles T. [2 ,3 ]
Miller, Jeffrey S. [1 ]
机构
[1] Univ Minnesota, Ctr Canc, Div Hematol Oncol & Transplantat, Minneapolis, MN 55455 USA
[2] Univ Kentucky, Dept Pathol & Lab Med, Lexington, KY 40536 USA
[3] Univ Kentucky, Dept Microbiol Immunol & Mol Genet, Lexington, KY 40536 USA
基金
美国国家卫生研究院;
关键词
DIFFERENTIATION;
D O I
10.4049/jimmunol.1100835
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
MicroRNAs (miRs) have recently been identified as important regulators of gene expression at the posttranscriptional level. Although it has clearly been established that miRs influence the ontogeny of several immune cell lineages, the role of individual miRs during NK cell development has not been described. In this study, we show that miR-181 expression levels have a profound impact on the development of human NK cells from CD34(+) hematopoietic progenitor cells and IFN-gamma production in primary CD56(+) NK cells. We also demonstrate that nemo-like kinase (NLK), an inhibitor of Notch signaling, is a target of miR-181 in NK cells, and knockdown of NLK mirrors the developmental effect of miR-181 overexpression. We conclude that miR-181 promotes NK cell development, at least in part, through the suppression of NLK, providing an important link between miRs and Notch signaling. The Journal of Immunology, 2011, 187: 6171-6175.
引用
收藏
页码:6171 / 6175
页数:5
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