Although the broad outlines of teleost immunity are known, the lack of molecular information concerning key cell surface markers (e.g. CD3, CD4, CD8) and cytokines (e.g. interferons and interleukins) has slowed progress. This collaborative pilot study intends to address this deficiency and to identify genes for catfish immune regulatory proteins and cell surface markers by differential display. To identify immune regulatory proteins, catfish peripheral blood leukocytes (PBLs) will be induced to express immune function genes and mRNAs from activated cultures will be compared to mRNAs from untreated cultures by differential display. RNAs from both populations will be reverse transcribed using arbitrary primers, amplified, resolved on sequencing gels, and visualized by autoradiography. After cloning and sequencing the amplicons, selectively expressed in activated cultures, their nucleotide or deduced amino acid sequences will be compared to known genes or gene products by BLAST analysis to determine whether differentially expressed amplicons encode immune-related gene products. To obtain full-size transcripts, amplicons encoding immune-related genes will be used to screen a cDNA library prepared from activated cultures. Putative immune functions will be characterized by Southern blot analysis to determine the number of copies per genome and Northern blot analysis to determine levels of constitutive and induced expression and the kinetics of expression. Genes of interest will be expressed and the resultant recombinant proteins used as antigen to develop specific antibodies. Western blot analysis will determine when, following induction, the protein is expressed and immunological staining will determine cell and tissue sites of expression. Successfully completed, this study will provide important new information that will further understanding of teleost immune responses, and perhaps provide insight into the origins of human immunity.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Minority Biomedical Research Support - MBRS (S06)
Project #
5S06GM008110-30
Application #
6650615
Study Section
Minority Programs Review Committee (MPRC)
Project Start
2002-09-01
Project End
2003-08-31
Budget Start
Budget End
Support Year
30
Fiscal Year
2002
Total Cost
$160,335
Indirect Cost
Name
Tougaloo College
Department
Type
DUNS #
City
Tougaloo
State
MS
Country
United States
Zip Code
39174
Cole, T J; Beckage, N E; Tan, F F et al. (2002) Parasitoid-host endocrine relations: self-reliance or co-optation? Insect Biochem Mol Biol 32:1673-9
Cole, Tracey J; Ramaswamy, Sonny B; Srinivasan, Asoka et al. (2002) Juvenile hormone catabolism and oviposition in the codling moth, Cydia pomonella, as functions of age, mating status, and hormone treatment. Arch Insect Biochem Physiol 49:10-21