The aim of this proposal is to identify cDNA clones corresponding to genes preferentially expressed in CD3- NK cells and other cells that express NK function and to understand the function of the corresponding gene products. A subtracted cDNA library enriched for cDNA clones associated with NK cells and NK/LAK activity will be prepared from a cloned NK cell (CD3-,CD16+,Leu19+) that expresses high-level NK/LAK function. A variety of screening methods will identify cDNA clones of interest within this library. Our first priority is to identify cDNA clones encoding cell surface molecules associated with NK cells and/or NK and LAK function. Second, we are interested in identifying clones encoding cell surface molecules expressed in both NK and T cells; this may identify molecules important in the regulation of NK function. Third, we are interested in clones that encode other molecules expressed preferentially in NK cells and other cells that express NK function. Two types of probes will be used to identify cDNA clones that encode membrane-bound components or secreted products. First, the subtracted library will be screened with a probe derived from poly-A+ RNA from membrane-bound polysomes of the cloned NK cell. Second, antisera prepared against the NK cell clone and absorbed with LCL will be used to probe the subtracted cDNA library prepared in a lambda-based expression vector. A long-term goal of this project is to use information and reagents obtained by molecular techniques to understand further the cell biology of NK cells, especially the generation and expression of NK/LAK activity. Whereas all genes to be studied will be derived from the NK clone described above, probing for expression of these genes in other cells, e.g. CD3+ cells with NK or NK and LAK function may help understand the genetic basis of these functions. Newly-defined genes will be sequenced and their expression studied in a variety of cell types; antisera/moAb will be made to proteins of interest. Although more difficult, we also plan to perform anti-sense (anti- mRNA) inhibition and transfection studies. We anticipate that these studies will provide information that will be useful as activated NK cells are used in clinical protocols.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI019007-11
Application #
2060837
Study Section
Experimental Immunology Study Section (EI)
Project Start
1992-07-01
Project End
1994-12-31
Budget Start
1993-01-01
Budget End
1994-12-31
Support Year
11
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02215
von Albertini, M A; Goodman, D J; Bach, F H (1996) Direct cell contact is required to induce expression of E-selectin and IL-8 secretion in pig endothelial cells by human natural killer cells. Transplant Proc 28:608
Goodman, D J; Von Albertini, M; Willson, A et al. (1996) Direct activation of porcine endothelial cells by human natural killer cells. Transplantation 61:763-71
Goodman, D J; von Albertini, M; Bach, F H (1996) Human natural killer cells induce expression of E-selectin and interleukin-8 mRNA in porcine endothelial cells. Transplant Proc 28:609
Adamkiewicz, T V; McSherry, C; Bach, F H et al. (1994) Natural killer lectin-like receptors have divergent carboxy-termini, distinct from C-type lectins. Immunogenetics 39:218
Turman, M A; Yabe, T; McSherry, C et al. (1993) Characterization of a novel gene (NKG7) on human chromosome 19 that is expressed in natural killer cells and T cells. Hum Immunol 36:34-40
Yabe, T; McSherry, C; Bach, F H et al. (1993) A multigene family on human chromosome 12 encodes natural killer-cell lectins. Immunogenetics 37:455-60
Houchins, J P; Kricek, F; Chujor, C S et al. (1993) Genomic structure of NKG5, a human NK and T cell-specific activation gene. Immunogenetics 37:102-7
Nelson, P J; Geller, R L; Podack, E et al. (1992) Molecular events in late stages of T-cell functional maturation. Scand J Immunol 35:311-20
Nelson, P J; Geller, R L; Bach, F H (1992) Gene expression in CD8 and CD4 T-cell populations following activation with the calcium ionophore A23187. Scand J Immunol 35:611-9
Houchins, J P; Yabe, T; McSherry, C et al. (1991) DNA sequence analysis of NKG2, a family of related cDNA clones encoding type II integral membrane proteins on human natural killer cells. J Exp Med 173:1017-20

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