A committed postselection precursor to natural TCRαβ + intraepithelial lymphocytes

Mucosal Immunol. 2018 Mar;11(2):333-344. doi: 10.1038/mi.2017.54. Epub 2017 Jul 26.

Abstract

The intestine is a major immune organ with several specialized lymphoid structures and immune cells. Among these are thymus-derived natural intraepithelial lymphocytes (IELs) that lack expression of the classical co-receptors CD4 or CD8αβ (double negative (DN)). Natural IELs are both αβ+ and γδ+ T cells that play important roles in the maintenance of the epithelial barrier at steady state and during inflammation. The transcription factor T-bet is essential for the peripheral development of natural IELs, but its role during thymic development has remained less clear. Here we show that a T-bet gradient in DN TCRαβ+NK1.1- thymocytes (IEL precursors (IELPs)) determines IEL fate in natural TCRαβ+ IELs. Employing T-bet ZsGreen reporter mice in in vitro cultures and in vivo transfer experiments, we demonstrate that with increasing expression of T-bet, DN TCRαβ+NK1.1- thymocytes are gradually restricted to a DN IEL fate. Furthermore, we show that the natural TCRαβ+ IELs seed the intestine within the first month of life. This in turn is preceded by the appearance of T-bet- and T-bet+ IELPs that egress from the thymus in a sphingosine-1-phosphate (S1P)-dependent manner. In summary, the use of T-bet reporter mice has enabled us to identify and refine an immediate and clearly committed postselection precursor of natural TCRαβ+ IELs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Cells, Cultured
  • Clonal Selection, Antigen-Mediated
  • Intestines / immunology*
  • Intraepithelial Lymphocytes / physiology*
  • Lysophospholipids / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Precursor Cells, T-Lymphoid / physiology*
  • Receptors, Antigen, T-Cell, alpha-beta / metabolism
  • Sphingosine / analogs & derivatives
  • Sphingosine / metabolism
  • T-Box Domain Proteins / genetics
  • T-Box Domain Proteins / metabolism
  • T-Lymphocytes / physiology*
  • Thymus Gland / physiology*

Substances

  • Lysophospholipids
  • Receptors, Antigen, T-Cell, alpha-beta
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • sphingosine 1-phosphate
  • Sphingosine