The thymus leukemia (TL) molecule is an oncofetal antigen encoded by a class I gene in the mouse major histocompatibility complex (MHC). The goal of the proposed experiments is to gain insight into the possible function(s) of the TL molecule. A series of experiments will compare TL to a transplantation antigen, to determine if TL can interact with CD8, if it can present antigen, and if it can educate a repertoire of TL-restricted T cells. An attempt will be made to demonstrate if TL presents antigen to intestinal epithelial lymphocytes. To determine if TL has any role in either T cell proliferation or maturation, two types of transgenic mice will be characterized. Both types have abnormally high expression of TL on either their mature T cells, or on all of their cells. Monoclonal antibodies will be used to monitor the number and maturity of T cells in these animals, and functional assays on these cells will be carried out. Cell transfer experiments will be performed to determine if the TL+ fraction of fetal liver cells is comprised of cells committed to the T cell lineage. Furthermore, the effect of crosslinking surface TL on Ca+2 flux, proliferation, Il-2 synthesis and the activation of protein kinases will be explored. The function of the MHC class Ib genes has been an enigma. TL is the product of a representative MHC class Ib gene that is of particular interest on account of its expression by transformed and immature cells. The proposed experiments utilize a battery of modern techniques to explore the possible role of the TL molecule, whether it be in immune surveillance or in lymphocyte differentiation. By extension, these data should contribute insight into the function of other members of the potentially important group of MHC class Ib molecules.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA052511-02
Application #
3197263
Study Section
Experimental Immunology Study Section (EI)
Project Start
1991-04-01
Project End
1994-03-31
Budget Start
1992-04-01
Budget End
1993-03-31
Support Year
2
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Akbari, Omid; Faul, John L; Hoyte, Elisabeth G et al. (2006) CD4+ invariant T-cell-receptor+ natural killer T cells in bronchial asthma. N Engl J Med 354:1117-29
Geissmann, Frederic; Cameron, Thomas O; Sidobre, Stephane et al. (2005) Intravascular immune surveillance by CXCR6+ NKT cells patrolling liver sinusoids. PLoS Biol 3:e113
Godfrey, Dale I; Kronenberg, Mitchell (2004) Going both ways: immune regulation via CD1d-dependent NKT cells. J Clin Invest 114:1379-88
Stenstrom, Martin; Skold, Markus; Ericsson, Anna et al. (2004) Surface receptors identify mouse NK1.1+ T cell subsets distinguished by function and T cell receptor type. Eur J Immunol 34:56-65
Akbari, Omid; Stock, Philippe; Meyer, Everett et al. (2003) Essential role of NKT cells producing IL-4 and IL-13 in the development of allergen-induced airway hyperreactivity. Nat Med 9:582-8
Hammond, Kirsten J L; Kronenberg, Mitchell (2003) Natural killer T cells: natural or unnatural regulators of autoimmunity? Curr Opin Immunol 15:683-9
Skold, Markus; Stenstrom, Martin; Sidobre, Stephane et al. (2003) MHC-dependent and -independent modulation of endogenous Ly49 receptors on NK1.1+ T lymphocytes directed by T-cell receptor type. Immunology 110:313-21
Matsuda, Jennifer L; Gapin, Laurent; Baron, Jody L et al. (2003) Mouse V alpha 14i natural killer T cells are resistant to cytokine polarization in vivo. Proc Natl Acad Sci U S A 100:8395-400
Crowe, Nadine Y; Uldrich, Adam P; Kyparissoudis, Konstantinos et al. (2003) Glycolipid antigen drives rapid expansion and sustained cytokine production by NK T cells. J Immunol 171:4020-7
Elewaut, Dirk; Shaikh, Raziya B; Hammond, Kirsten J L et al. (2003) NIK-dependent RelB activation defines a unique signaling pathway for the development of V alpha 14i NKT cells. J Exp Med 197:1623-33

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