Canine models of human diseases have been used to study autoimmune thyroiditis, gluten-sensitive enteropathy, narcolepsy, complement deficiencies, and solid organ and hematopoietic progenitor cell transplants. Of paramount importance to comprehending immune-related diseases and transplantation immunology is an understanding of the MHC. In spite of the dog's usefulness in research, molecular and biochemical analyses of the canine MHC (termed DLA) have lagged behind those of the human MHC (HLA) and the murine MHC (H2) regions, as well as the MHC regions of various agricultural animals. The objective of this application is to develop a comprehensive understanding of the structure, polymorphism, and function of the canine class I and class II MHC genes. The specific goals are: 1) develop a DNA-based histocompatibility typing system for polymorphic class I and class II loci applicable to all dogs; 2) determine the structure and organization of the canine MHC by molecular mapping; and 3) identify tissues expressing class I proteins using newly generated monoclonal antibodies (MAbs). Histocompatibility typing for class I and class II genes will be performed using locus specific amplification and separation of alleles by single-strand conformational polymorphism (SSCP) gels. Pulsed-field gel electrophoresis (PFGE) with locus-specific probes will be used to determine the molecular organization of the DLA class I and class 11 gene families. A cosmid library will be constructed from a canine-hamster hybrid cell line containing a few dog chromosomes, one of which contains the DLA region. This library will be useful for mapping as well as identifying new genes within the DLA region. Class I expression will be analyzed at the protein level. Cell lines expressing canine class I genes will be produced, and reactive MAbs generated to be used in fluorescent activated cell sorting (FACS), immunoprecipitation, and immunohistochemistry studies. Class II expression will be initially studied using existing cross-reactive MAbs.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Resource-Related Research Projects (R24)
Project #
7R24RR012558-04
Application #
6321832
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1997-09-30
Project End
2002-08-31
Budget Start
2000-01-15
Budget End
2000-08-31
Support Year
4
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Thomas Jefferson University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
061197161
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
Wagner, J L; Palti, Y; DiDario, D et al. (2005) Sequence of the canine major histocompatibility complex region containing non-classical class I genes. Tissue Antigens 65:549-55
Wagner, J L (2003) Molecular organization of the canine major histocompatibility complex. J Hered 94:23-6
Wagner, J L; Sarmiento, U M; Storb, R (2002) Cellular, serological, and molecular polymorphism of the class I and class II loci of the canine Major Histocompatibility Complex. Tissue Antigens 59:205-10
Wagner, J L; Storb, R; Storer, B et al. (2000) DLA-DQB1 alleles and bone marrow transplantation experiments in narcoleptic dogs. Tissue Antigens 56:223-31
Wagner, J L; Creer, S A; Storb, R (2000) Dog class I gene DLA-88 histocompatibility typing by PCR-SSCP and sequencing. Tissue Antigens 55:564-7
Wagner, J L; Burnett, R C; Storb, R (1999) Organization of the canine major histocompatibility complex: current perspectives. J Hered 90:35-8