Development of the adaptive immune response requires generation of a T cell repertoire capable of recognizing a wide range of potential pathogens. However, this anticipatory repertoire has to be generated without ever seeing these pathogens. This is achieved by the process of positive selection of T cells in the thymus, which ensures the ability of a TCR to recognize peptide antigens presented by self-MHC molecules. Positive selection, which takes several days to complete, requires a sustained signal through Ca2+ and Erk and involves a weak interaction between a TCR on a thymocyte and a self-peptide/MHC complex on the surface of a cortical epithelial cell. We have recently identified a naturally occurring positive selecting self-peptide for AND CD4+ T cells, gp250. The solution 3D KD of the gp250/I-Ek:AND interaction was shown to be extremely weak. Despite its apparent weak affinity, gp250/I-Ek was able to induce a sustained Ca2+ signal and in vitro positive selection of AND thymocytes, whereas, the MCC agonist induced a transient signal, and negative selection. It is not known how a weak TCR:pMHC interaction can transduce sustained signaling in thymocytes. Essentially nothing is known about the molecular details for a TCR:positive selecting pMHC ligand interaction.
In Aim I, we propose studies to determine biophysically and structurally how the AND TCR binds to the positive selecting gp250/I-Ek ligand in comparison to the agonist ligand, MCC/I-Ek. We will determine the 2D affinity of these ligands as well as identify the threshold of affinity between positive and negative selection. The structural details of how the AND TCR binds gp250/I-Ek and MCC/I-Ek will be studied using a series of I-Ek point mutants, and the solving the crystal structures of the AND:gp250/I-Ek and AND:MCC/I-Ek co-complexes. The studies in Aim II investigate the novel observation that a voltage-gated sodium channel (composed of the SCN5a pore subunit and SCN4b regulatory subunit) induces a sustained Ca2+ influx and positive selection of AND T cells. Specific inhibition of the voltage gated sodium channel inhibited a gp250 stimulated sustained Ca2+ influx signal, and importantly blocked positive selection of AND thymocytes in reaggregate cultures. shRNA knockdown of SCN5a inhibited CD4 T cell positive selection in vivo. We hypothesize that a voltage gated sodium channel is critically involved in positive selection by activating a voltage gated Ca2+ channel in thymocytes, resulting in weak ligands being able to induce a sustained Ca2+ signal. The mechanism by which SCN5a/SCN4b are affecting signaling in thymocytes during positive selection will be determined electrophysiologically and biologically, and will involve the generation of conditional knockout mice for both genes. These studies will provide key new insights into how the process of positive selection occurs at a structural and signaling level, with the possibility of yielding molecular targets for the manipulation of unwanted T cells, including T cells involved in autoimmunity.

Public Health Relevance

Recognition and signaling in positive selection of CD4+ T cells Project Narrative A long desired goal of immunologists is a complete understanding of how an effective adaptive immune system develops in the absent of the antigens it is designed to recognize. Positive selection of T cells in the thymus involves weak interactions between a T cell receptor and a self-peptide/MHC ligand. We have developed a positive selecting model involving a naturally occurring self peptide (gp250) and the AND T cell and propose studies to investigate in detail the recognition of the AND:gp250/I-Ek interaction. We have also made the novel discovery that a voltage gated sodium channel is involved positive selection, and experiments are proposed to determine how this channel can lead to sustained T cell signaling required for positive selection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI024157-27
Application #
8636968
Study Section
Cellular and Molecular Immunology - B Study Section (CMIB)
Program Officer
Chiodetti, Lynda
Project Start
1987-04-01
Project End
2017-04-30
Budget Start
2014-05-01
Budget End
2015-04-30
Support Year
27
Fiscal Year
2014
Total Cost
$380,000
Indirect Cost
$130,000
Name
Washington University
Department
Pathology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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