RORα is a critical checkpoint for T cell and ILC2 commitment in the embryonic thymus

Nat Immunol. 2021 Feb;22(2):166-178. doi: 10.1038/s41590-020-00833-w. Epub 2021 Jan 11.

Abstract

Type 2 innate lymphoid cells (ILC2) contribute to immune homeostasis, protective immunity and tissue repair. Here we demonstrate that functional ILC2 cells can arise in the embryonic thymus from shared T cell precursors, preceding the emergence of CD4+CD8+ (double-positive) T cells. Thymic ILC2 cells migrated to mucosal tissues, with colonization of the intestinal lamina propria. Expression of the transcription factor RORα repressed T cell development while promoting ILC2 development in the thymus. From RNA-seq, assay for transposase-accessible chromatin sequencing (ATAC-seq) and chromatin immunoprecipitation followed by sequencing (ChIP-seq) data, we propose a revised transcriptional circuit to explain the co-development of T cells and ILC2 cells from common progenitors in the thymus. When Notch signaling is present, BCL11B dampens Nfil3 and Id2 expression, permitting E protein-directed T cell commitment. However, concomitant expression of RORα overrides the repression of Nfil3 and Id2 repression, allowing ID2 to repress E proteins and promote ILC2 differentiation. Thus, we demonstrate that RORα expression represents a critical checkpoint at the bifurcation of the T cell and ILC2 lineages in the embryonic thymus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic-Leucine Zipper Transcription Factors / genetics
  • Basic-Leucine Zipper Transcription Factors / metabolism
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism*
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / metabolism*
  • Cell Differentiation*
  • Cell Lineage*
  • Cell Movement
  • Cells, Cultured
  • Coculture Techniques
  • Female
  • Gene Expression Regulation, Developmental
  • Immunity, Innate*
  • Inhibitor of Differentiation Protein 2 / genetics
  • Inhibitor of Differentiation Protein 2 / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nuclear Receptor Subfamily 1, Group F, Member 1 / genetics
  • Nuclear Receptor Subfamily 1, Group F, Member 1 / metabolism*
  • Organ Culture Techniques
  • Phenotype
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Signal Transduction
  • Thymocytes / immunology
  • Thymocytes / metabolism*
  • Thymus Gland / embryology
  • Thymus Gland / immunology
  • Thymus Gland / metabolism*
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism

Substances

  • Basic-Leucine Zipper Transcription Factors
  • Bcl11b protein, mouse
  • Idb2 protein, mouse
  • Inhibitor of Differentiation Protein 2
  • Nfil3 protein, mouse
  • Nuclear Receptor Subfamily 1, Group F, Member 1
  • Repressor Proteins
  • Rora protein, mouse
  • Tumor Suppressor Proteins