The molecular signature of CD8+ T cells undergoing deletional tolerance

Author:

Parish Ian A.123,Rao Sudha4,Smyth Gordon K.1,Juelich Torsten4,Denyer Gareth S.5,Davey Gayle M.16,Strasser Andreas1,Heath William R.16

Affiliation:

1. Walter and Eliza Hall Institute of Medical Research, Parkville, Australia;

2. Department of Medical Biology, University of Melbourne, Parkville, Australia;

3. Immunobiology Department, Yale School of Medicine, New Haven, CT;

4. Division of Immunology and Genetics, John Curtin School of Medical Research, Australian National University, Acton, Australia;

5. School of Molecular and Microbial Biosciences, University of Sydney, Sydney, Australia; and

6. Department of Microbiology and Immunology, University of Melbourne, Parkville, Australia

Abstract

Abstract Peripheral tolerance induction is critical for the maintenance of self-tolerance and can be mediated by immunoregulatory T cells or by direct induction of T-cell anergy or deletion. Although the molecular processes underlying anergy have been extensively studied, little is known about the molecular basis for peripheral T-cell deletion. Here, we determined the gene expression signature of peripheral CD8+ T cells undergoing deletional tolerance, relative to those undergoing immunogenic priming or lymphopenia-induced proliferation. From these data, we report the first detailed molecular signature of cells undergoing deletion. Consistent with defective cytolysis, these cells exhibited deficiencies in granzyme up-regulation. Furthermore, they showed antigen-driven Bcl-2 down-regulation and early up-regulation of the proapoptotic protein Bim, consistent with the requirement of this BH3-only protein for peripheral T-cell deletion. Bim up-regulation was paralleled by defective interleukin-7 receptor α (IL-7Rα) chain reexpression, suggesting that Bim-dependent death may be triggered by loss of IL-7/IL-7R signaling. Finally, we observed parallels in molecular signatures between deletion and anergy, suggesting that these tolerance pathways may not be as molecularly distinct as previously surmised.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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