Characterization of T Cell Differentiation in the Murine Gut

Author:

Lambolez Florence1,Azogui Orly2,Joret Anne-Marie1,Garcia Corinne3,von Boehmer Harald4,Di Santo James5,Ezine Sophie1,Rocha Benedita1

Affiliation:

1. Institut National de la Santé et de la Recherche Médicale (INSERM) U345, Institut Necker, 75730 Paris, France

2. E9925, Institut Necker, 75730 Paris, France

3. U373, Institut Necker, 75730 Paris, France

4. Harvard Medical School, Dana-Farber Cancer Institute, Boston, MA 02115

5. Institut Pasteur, 75015 Paris, France

Abstract

Gut intraepithelial CD8 T lymphocytes (T-IEL) are distinct from thymus-derived cells and are thought to derive locally from cryptopatch (CP) precursors. The intermediate stages of differentiation between CP and mature T-IEL were not identified, and the local differentiation process was not characterized. We identified and characterized six phenotypically distinct lineage-negative populations in the CP and the gut epithelium: (a) we determined the kinetics of their generation from bone marrow precursors; (b) we quantified CD3-ϵ, recombination activating gene (Rag)-1, and pre-Tα mRNAs expression at single cell level; (c) we characterized TCR-β, -γ, and -α locus rearrangements; and (d) we studied the impact of different mutations on the local differentiation. These data allowed us to establish a sequence of T cell precursor differentiation in the gut. We also observed that the gut differentiation varied from that of the thymus by a very low frequency of pre-Tα chain mRNA expression, a different kinetics of Rag-1 mRNA expression, and a much higher impact of CD3 ϵ/δ and pre-Tα deficiencies. Finally, only 3% of CP cells were clearly involved in T cell differentiation, suggesting that these structures may have additional physiological roles in the gut.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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