TY - JOUR
T1 - MicroRNA-15/16 antagonizes Myb to control NK cell maturation
AU - Sullivan, Ryan P.
AU - Leong, Jeffrey W.
AU - Schneider, Stephanie E.
AU - Ireland, Aaron R.
AU - Berrien-Elliott, Melissa M.
AU - Singh, Anvita
AU - Schappe, Timothy
AU - Jewell, Brea A.
AU - Sexl, Veronika
AU - Fehniger, Todd A.
N1 - Publisher Copyright:
© 2015 by The American Association of Immunologists, Inc.
PY - 2015/9/15
Y1 - 2015/9/15
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84941776166&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.1500949
DO - 10.4049/jimmunol.1500949
M3 - Article
C2 - 26268657
AN - SCOPUS:84941776166
SN - 0022-1767
VL - 195
SP - 2806
EP - 2817
JO - Journal of Immunology
JF - Journal of Immunology
IS - 6
ER -