| Literature DB >> 31402259 |
Melissa M Berrien-Elliott1, Yaping Sun2, Carly Neal1, Aaron Ireland1, Maria C Trissal1, Ryan P Sullivan1, Julia A Wagner1, Jeffrey W Leong1, Pamela Wong1, Annelise Y Mah-Som3, Terrence N Wong1, Timothy Schappe1, Catherine R Keppel1, Victor S Cortez4, Efstathios G Stamatiades5, Ming O Li5, Marco Colonna4, Daniel C Link1, Anthony R French3, Megan A Cooper3, Wei-Le Wang6, Mark P Boldin6, Pavan Reddy2, Todd A Fehniger7.
Abstract
Natural killer (NK) cells are cytotoxic type 1 innate lymphoid cells (ILCs) that defend against viruses and mediate anti-tumor responses, yet mechanisms controlling their development and function remain incompletely understood. We hypothesized that the abundantly expressed microRNA-142 (miR-142) is a critical regulator of type 1 ILC biology. Interleukin-15 (IL-15) signaling induced miR-142 expression, whereas global and ILC-specific miR-142-deficient mice exhibited a cell-intrinsic loss of NK cells. Death of NK cells resulted from diminished IL-15 receptor signaling within miR-142-deficient mice, likely via reduced suppressor of cytokine signaling-1 (Socs1) regulation by miR-142-5p. ILCs persisting in Mir142-/- mice demonstrated increased expression of the miR-142-3p target αV integrin, which supported their survival. Global miR-142-deficient mice exhibited an expansion of ILC1-like cells concurrent with increased transforming growth factor-β (TGF-β) signaling. Further, miR-142-deficient mice had reduced NK-cell-dependent function and increased susceptibility to murine cytomegalovirus (MCMV) infection. Thus, miR-142 critically integrates environmental cues for proper type 1 ILC homeostasis and defense against viral infection.Entities:
Keywords: IL-15; ILC1-like cells; NK cells; cytokine receptors; innate lymphoid cells; integrin; microRNA-142; murine cytomegalovirus; tissue resident
Mesh:
Substances:
Year: 2019 PMID: 31402259 PMCID: PMC6750984 DOI: 10.1016/j.immuni.2019.06.016
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745