Nfil3 is crucial for development of innate lymphoid cells and host protection against intestinal pathogens

J Exp Med. 2014 Aug 25;211(9):1723-31. doi: 10.1084/jem.20140212. Epub 2014 Aug 11.

Abstract

The bZIP transcription factor Nfil3 (also known as E4BP4) is required for the development of natural killer (NK) cells and type 1 innate lymphoid cells (ILC1s). We find that Nfil3 plays a critical role in the development of other mucosal tissue-associated innate lymphocytes. Type 3 ILCs (ILC3s), including lymphoid tissue inducer (LTi)-like cells, are severely diminished in both numbers and function in Nfil3-deficient mice. Using mixed bone marrow chimeric mice, we demonstrate that Nfil3 is critical for normal development of gut-associated ILC3s in a cell-intrinsic manner. Furthermore, Nfil3 deficiency severely compromises intestinal innate immune defense against acute bacterial infection with Citrobacter rodentium and Clostridium difficile. Nfil3 deficiency resulted in a loss of the recently identified ILC precursor, yet conditional ablation of Nfil3 in the NKp46(+) ILC3 subset did not perturb ILC3 numbers, suggesting that Nfil3 is required early during ILC3 development but not for lineage maintenance. Lastly, a marked defect in type 2 ILCs (ILC2s) was also observed in the lungs and visceral adipose tissue of Nfil3-deficient mice, revealing a general requirement for Nfil3 in the development of all ILC lineages.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Ly / genetics
  • Antigens, Ly / immunology
  • Basic-Leucine Zipper Transcription Factors / deficiency
  • Basic-Leucine Zipper Transcription Factors / genetics
  • Basic-Leucine Zipper Transcription Factors / immunology*
  • Cell Lineage / genetics
  • Cell Lineage / immunology
  • Citrobacter rodentium / immunology
  • Citrobacter rodentium / pathogenicity
  • Clostridioides difficile / immunology
  • Clostridioides difficile / pathogenicity
  • Host-Pathogen Interactions / genetics
  • Host-Pathogen Interactions / immunology*
  • Immunity, Innate* / genetics
  • Immunity, Mucosal / genetics
  • Intestines / immunology
  • Intestines / microbiology
  • Killer Cells, Natural / immunology
  • Lymphocyte Subsets / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Natural Cytotoxicity Triggering Receptor 1 / genetics
  • Natural Cytotoxicity Triggering Receptor 1 / immunology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Transplantation Chimera / immunology

Substances

  • Antigens, Ly
  • Basic-Leucine Zipper Transcription Factors
  • Natural Cytotoxicity Triggering Receptor 1
  • Ncr1 protein, mouse
  • Nfil3 protein, mouse
  • RNA, Messenger