Stimulation of interleukin-2 (IL-2) producing T cell clones with antigen and MHC class II molecules (Ia molecules) in planar lipid membranes or on chemically-modified antigen-presenting cells (APC) results in a state of long lasting proliferative nonresponsiveness to subsequent antigen stimulation in the presence of normal APC. Our recent experiments have shown that the induction of this take state takes place when T cell receptor occupancy occurs in the absence of a critical costimulatory signal delivered by the APC. When this signal is provided in the form of allogeneic APC, it prevents the induction of nonresponsiveness and stimulates the T cell to proliferate. A biochemical analysis of second messenger signals inside the cell revealed that the costimulatory signal does not pass through protein kinase c activation nor through the calcium-dependent calmodulin-mediated pathway, both of which are stimulated by T cell receptor occupancy. These results suggest that the T cell requires stimulation via a third biochemical pathway in order to make a full proliferative response. Lack of the third signal results instead in the induction of the nonresponsive state.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000485-03
Application #
3818259
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Niaid Extramural Activities
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Johnson, Andy L; Aravind, L; Shulzhenko, Natalia et al. (2009) Themis is a member of a new metazoan gene family and is required for the completion of thymocyte positive selection. Nat Immunol 10:831-9
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Safford, Meredith; Collins, Samuel; Lutz, Michael A et al. (2005) Egr-2 and Egr-3 are negative regulators of T cell activation. Nat Immunol 6:472-80
Cho, Eun-Gyung; Schwartz, Ronald H; Kim, Moon G (2005) Shedding of membrane epithin is blocked without LDLRA4 and its protease activation site. Biochem Biophys Res Commun 327:328-34

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