Lineage Relationship Analysis of RORγt + Innate Lymphoid Cells

Author:

Sawa Shinichiro12,Cherrier Marie12,Lochner Matthias123,Satoh-Takayama Naoko45,Fehling Hans Jörg6,Langa Francina7,Di Santo James P.45,Eberl Gérard12

Affiliation:

1. Lymphoid Tissue Development Unit, Institut Pasteur, 75724 Paris, France.

2. CNRS, URA1961, 75724 Paris, France.

3. Institute of Infection Immunology, TWINCORE, Centre for Experimental and Clinical Infection Research; a joint venture between the Medical School Hannover and the Helmholtz Centre for Infection Research, Hannover, Germany.

4. Innate Immunity Unit, Institut Pasteur, 75724 Paris, France.

5. Inserm, U668, 75724 Paris, France.

6. Institute of Immunology, University Clinics Ulm, Ulm, Germany.

7. Centre Ingénieurie Génétique Murine, Institut Pasteur, 75724 Paris, France.

Abstract

Innate Innit? Innate lymphocytes (ILCs) are a recently described population of immune cells that produce cytokines like those associated with T helper cells, but lack the recombined antigen receptors characteristic of T cells. Again, like some T helper cell lineages, a proportion of ILCs express the transcription factor RORγt. These include lymphoid tissue inducer (LTi) cells required for fetal lymphoid tissue organogenesis and a population of natural killer (NK)–like cells that function in gut immune responses. Sawa et al. (p. 665 ; see the Perspective by Veldhoen and Withers ) wondered whether the RORγt-expressing ILCs all develop from the same progenitor population. Indeed, they found a fetal liver progenitor that gave rise to several phenotypically distinct populations. However, the LTi cells were not progenitors for the NK-like cells. It seems the trajectory of different ILC populations is developmentally regulated, and postnatally ILCs are favored that play a role in intestinal defense before the gut is fully colonized by intestinal microbiota.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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