4.6 Article

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

Journal

JOURNAL OF IMMUNOLOGY
Volume 195, Issue 6, Pages 2806-2817

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1500949

Keywords

-

Categories

Funding

  1. National Institutes of Health [T32 HL007088, F32 CA200253, R01AI102924]
  2. American Society of Hematology Foundation
  3. Howard Hughes Medical Institute

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available