Literature DB >> 26268657

MicroRNA-15/16 Antagonizes Myb To Control NK Cell Maturation.

Ryan P Sullivan1, Jeffrey W Leong1, Stephanie E Schneider1, Aaron R Ireland1, Melissa M Berrien-Elliott1, Anvita Singh1, Timothy Schappe1, Brea A Jewell1, Veronika Sexl2, Todd A Fehniger3.   

Abstract

NK cells develop in the bone marrow and complete their maturation in peripheral organs, but the molecular events controlling maturation are incompletely understood. The miR-15/16 family of microRNA regulates key cellular processes and is abundantly expressed in NK cells. In this study, we identify a critical role for miR-15/16 in the normal maturation of NK cells using a mouse model of NK-specific deletion, in which immature NK cells accumulate in the absence of miR-15/16. The transcription factor c-Myb (Myb) is expressed preferentially by immature NK cells, is a direct target of miR-15/16, and is increased in 15a/16-1 floxed knockout NK cells. Importantly, maturation of 15a/16-1 floxed knockout NK cells was rescued by Myb knockdown. Moreover, Myb overexpression in wild-type NK cells caused a defective NK cell maturation phenotype similar to deletion of miR-15/16, and Myb overexpression enforces an immature NK cell transcriptional profile. Thus, miR-15/16 regulation of Myb controls the NK cell maturation program.
Copyright © 2015 by The American Association of Immunologists, Inc.

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Year:  2015        PMID: 26268657      PMCID: PMC4561212          DOI: 10.4049/jimmunol.1500949

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  54 in total

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