Conditional deletion of cytokine receptor chains reveals that IL-7 and IL-15 specify CD8 cytotoxic lineage fate in the thymus

Author:

McCaughtry Tom M.1,Etzensperger Ruth1,Alag Amala1,Tai Xuguang1,Kurtulus Sema2,Park Jung-Hyun1,Grinberg Alex3,Love Paul3,Feigenbaum Lionel4,Erman Batu2,Singer Alfred1

Affiliation:

1. Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892

2. Biological Sciences and Bioengineering Program, Faculty of Engineering and Natural Sciences, Sabanci University, Istanbul 34956, Turkey

3. Laboratory of Mammalian Genes and Development, National Institute of Child Health and Human Development, Bethesda, MD 20892

4. SAIC-Frederick, National Cancer Institute–Frederick Cancer Research and Development Center, Frederick, MD 21702

Abstract

The thymus generates T cells with diverse specificities and functions. To assess the contribution of cytokine receptors to the differentiation of T cell subsets in the thymus, we constructed conditional knockout mice in which IL-7Rα or common cytokine receptor γ chain (γc) genes were deleted in thymocytes just before positive selection. We found that γc expression was required to signal the differentiation of MHC class I (MHC-I)–specific thymocytes into CD8+ cytotoxic lineage T cells and into invariant natural killer T cells but did not signal the differentiation of MHC class II (MHC-II)–specific thymocytes into CD4+ T cells, even into regulatory Foxp3+CD4+ T cells which require γc signals for survival. Importantly, IL-7 and IL-15 were identified as the cytokines responsible for CD8+ cytotoxic T cell lineage specification in vivo. Additionally, we found that small numbers of aberrant CD8+ T cells expressing Runx3d could arise without γc signaling, but these cells were developmentally arrested before expressing cytotoxic lineage genes. Thus, γc-transduced cytokine signals are required for cytotoxic lineage specification in the thymus and for inducing the differentiation of MHC-I–selected thymocytes into functionally mature T cells.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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