The Ly-6 super family of proteins has common structural cysteine motifs and is GPI anchored to the cell surface. The functions associated with them include cell:cell adhesion, regulation of responses to cytokines, complement inhibition and cell activation perhaps resulting from interactions with ligands and adjacent cell surface receptors. The Ly-6 antigens are expressed on distinct cell populations and thus transcriptional regulation is an important factor determining their expression patterns. Cytokines, especially IFNs, can significantly alter the expression of Ly-6 in a cell type specific manner. The objective of these studies is to define the function of the subset of Ly-6 antigens that are associated with hematopoietic lineages and assess what contribution they may have on the differentiation process of these lineages.
The specific aims of the proposal are: (1) to identify the ligand(s) for Ly-6 antigens; (2) to characterize the relationship of Ly-6 antigen expression with the development of distinct hematopoietic lineages using Pax5-/- cells; (3) to characterize the effects of the Ly-6 signaling pathway on effector function and cell cycle regulation in Th2, Th1 and CD8 T cells; (4) to further characterize tissue specific transcriptional regulation of Ly-6A/E and characterize additional novel family members and (5) to generate and characterize the phenotype of Ly-6C and Ly-6I knockout mice. We have observed that Ly-6I together with Ly-6AIE, Ly-6C or Ly-6G may define distinct cell populations and we will determine whether Ly-6I can be used to further define hematopoietic stem cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM040924-10
Application #
6286223
Study Section
Allergy and Immunology Study Section (ALY)
Program Officer
Marino, Pamela
Project Start
1989-07-01
Project End
2004-11-30
Budget Start
2000-12-01
Budget End
2001-11-30
Support Year
10
Fiscal Year
2001
Total Cost
$284,458
Indirect Cost
Name
Yale University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Kennedy, S P; Rollins, S A; Burton, W V et al. (1994) Protection of porcine aortic endothelial cells from complement-mediated cell lysis and activation by recombinant human CD59. Transplantation 57:1494-501
Lee, S K; Su, B; Maher, S E et al. (1994) Ly-6A is required for T cell receptor expression and protein tyrosine kinase fyn activity. EMBO J 13:2167-76
Murray, A G; Khodadoust, M M; Pober, J S et al. (1994) Porcine aortic endothelial cells activate human T cells: direct presentation of MHC antigens and costimulation by ligands for human CD2 and CD28. Immunity 1:57-63
Lee, S K; Shaw, A; Maher, S E et al. (1994) p59fyn tyrosine kinase regulates p56lck tyrosine kinase activity and early TCR-mediated signaling. Int Immunol 6:1621-7
Khan, K D; Shuai, K; Lindwall, G et al. (1993) Induction of the Ly-6A/E gene by interferon alpha/beta and gamma requires a DNA element to which a tyrosine-phosphorylated 91-kDa protein binds. Proc Natl Acad Sci U S A 90:6806-10
Ninomiya, H; Stewart, B H; Rollins, S A et al. (1992) Contribution of the N-linked carbohydrate of erythrocyte antigen CD59 to its complement-inhibitory activity. J Biol Chem 267:8404-10
Zhao, J; Rollins, S A; Maher, S E et al. (1991) Amplified gene expression in CD59-transfected Chinese hamster ovary cells confers protection against the membrane attack complex of human complement. J Biol Chem 266:13418-22
Su, B; Waneck, G L; Flavell, R A et al. (1991) The glycosyl phosphatidylinositol anchor is critical for Ly-6A/E-mediated T cell activation. J Cell Biol 112:377-84
Zhang, F; Crise, B; Su, B et al. (1991) Lateral diffusion of membrane-spanning and glycosylphosphatidylinositol-linked proteins: toward establishing rules governing the lateral mobility of membrane proteins. J Cell Biol 115:75-84
Philbrick, W M; Maher, S E; Bridgett, M M et al. (1990) A recombination event in the 5' flanking region of the Ly-6C gene correlates with impaired expression in the NOD, NZB and ST strains of mice. EMBO J 9:2485-92

Showing the most recent 10 out of 12 publications