miR-17∼92 family clusters control iNKT cell ontogenesis via modulation of TGF-β signaling

Proc Natl Acad Sci U S A. 2016 Dec 20;113(51):E8286-E8295. doi: 10.1073/pnas.1612024114. Epub 2016 Dec 5.

Abstract

Invariant natural killer T cells (iNKT) cells are T lymphocytes displaying innate effector functions, acquired through a distinct thymic developmental program regulated by microRNAs (miRNAs). Deleting miRNAs by Dicer ablation (Dicer KO) in thymocytes selectively impairs iNKT cell survival and functional differentiation. To unravel this miRNA-dependent program, we systemically identified transcripts that were differentially expressed between WT and Dicer KO iNKT cells at different differentiation stages and predicted to be targeted by the iNKT cell-specific miRNAs. TGF-β receptor II (TGF-βRII), critically implicated in iNKT cell differentiation, was found up-regulated in iNKT Dicer KO cells together with enhanced TGF-β signaling. miRNA members of the miR-17∼92 family clusters were predicted to target Tgfbr2 mRNA upon iNKT cell development. iNKT cells lacking all three miR-17∼92 family clusters (miR-17∼92, miR-106a∼363, miR-106b∼25) phenocopied both increased TGF-βRII expression and signaling, and defective effector differentiation, displayed by iNKT Dicer KO cells. Consistently, genetic ablation of TGF-β signaling in the absence of miRNAs rescued iNKT cell differentiation. These results elucidate the global impact of miRNAs on the iNKT cell developmental program and uncover the targeting of a lineage-specific cytokine signaling by miRNAs as a mechanism regulating innate-like T-cell development and effector differentiation.

Keywords: CD1d; NKT cells; TGF-β; development; miRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD1d / metabolism
  • Cell Differentiation
  • Cytokines / metabolism
  • DEAD-box RNA Helicases / genetics
  • Gene Expression Profiling
  • Genetic Complementation Test
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • MicroRNAs / genetics*
  • Multigene Family
  • Natural Killer T-Cells / cytology*
  • Phenotype
  • RNA, Messenger / metabolism
  • Ribonuclease III / genetics
  • Signal Transduction
  • Thymus Gland / metabolism
  • Transforming Growth Factor beta / metabolism*

Substances

  • Antigens, CD1d
  • Cd1d1 protein, mouse
  • Cytokines
  • MIRN17-92 microRNA, mouse
  • MicroRNAs
  • RNA, Messenger
  • Transforming Growth Factor beta
  • Dicer1 protein, mouse
  • Ribonuclease III
  • DEAD-box RNA Helicases