Deciphering the Innate Lymphoid Cell Transcriptional Program

Cell Rep. 2016 Oct 4;17(2):436-447. doi: 10.1016/j.celrep.2016.09.025.

Abstract

Innate lymphoid cells (ILCs) are enriched at mucosal surfaces, where they provide immune surveillance. All ILC subsets develop from a common progenitor that gives rise to pre-committed progenitors for each of the ILC lineages. Currently, the temporal control of gene expression that guides the emergence of these progenitors is poorly understood. We used global transcriptional mapping to analyze gene expression in different ILC progenitors. We identified PD-1 to be specifically expressed in PLZF+ ILCp and revealed that the timing and order of expression of the transcription factors NFIL3, ID2, and TCF-1 was critical. Importantly, induction of ILC lineage commitment required only transient expression of NFIL3 prior to ID2 and TCF-1 expression. These findings highlight the importance of the temporal program that permits commitment of progenitors to the ILC lineage, and they expand our understanding of the core transcriptional program by identifying potential regulators of ILC development.

Keywords: development; immunity; innate; innate lymphoid cells; transcription factors.

MeSH terms

  • Animals
  • Basic-Leucine Zipper Transcription Factors / genetics*
  • Basic-Leucine Zipper Transcription Factors / immunology
  • Bone Marrow Cells / immunology
  • Cell Differentiation / genetics
  • Cell Differentiation / immunology
  • Cell Lineage / immunology
  • Gene Expression Regulation
  • Hepatocyte Nuclear Factor 1-alpha / genetics*
  • Hepatocyte Nuclear Factor 1-alpha / immunology
  • Immunity, Innate / genetics
  • Immunity, Innate / immunology*
  • Killer Cells, Natural / immunology
  • Lymphocytes / immunology*
  • Mice
  • Programmed Cell Death 1 Receptor / genetics*
  • Programmed Cell Death 1 Receptor / immunology
  • Transcription Factors / genetics
  • Transcription Factors / immunology

Substances

  • Basic-Leucine Zipper Transcription Factors
  • Hepatocyte Nuclear Factor 1-alpha
  • Hnf1a protein, mouse
  • Nfil3 protein, mouse
  • Pdcd1 protein, mouse
  • Programmed Cell Death 1 Receptor
  • Transcription Factors