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Diabetes, Vol 42, Issue 5 688-695, Copyright © 1993 by American Diabetes Association
An RT6a gene is transcribed and translated in lymphopenic diabetes-prone BB rats
L Crisa, P Sarkar, DJ Waite, FH Friedrich, , TV Rajan, JP Mordes, ES Handler, HG Thiele, AA Rossini and al. et
Diabetes Division, University of Massachusetts, Worcester Medical Center 01605.
T-cells expressing the RT6 surface alloantigen appear to perform important
immunoregulatory functions in the rat. Diabetes-prone BB rats lack
circulating RT6+ T-cells and spontaneously develop autoimmune diabetes
mellitus and thyroiditis. The coisogenic diabetes-resistant BB rat does
circulate RT6+ T-cells and is free of disease. Transfusions leading to
engraftment of RT6+ T-cells prevent both diabetes and thyroiditis in the
diabetes-prone rat. To investigate the absence of this subset in the
lymphopenic BB rat, we used both molecular and biochemical procedures and
made the following observations: 1) an mRNA encoding RT6 protein is present
in diabetes-prone spleen cells; 2) nucleotide sequencing of this transcript
reveals an intact coding sequence for the RT6.1 alloantigen; 3) sensitive
chemiluminescent assay of diabetes-prone lymph node cell detergent extracts
shows that diabetes-prone RT6 mRNA is translated in vivo; 4)
quantitatively, diabetes-prone lymph node cells express < or = 10% of
the RT6.1 protein found on similar numbers of diabetes-resistant BB cells;
and 5) finally, we obtained evidence of an intact phosphatidylinositol
linkage of the molecule to the cell surface and successfully
immunoprecipitated the phosphatidylinositol-linked protein with DS4.23
monoclonal antibody, indicating that the RT6.1 antigen is correctly
processed and folded in diabetes-prone lymph node cells. We conclude that
the near total absence of RT6+ T-cells in the diabetes-prone BB rat is
unlikely to be because of a defect in RT6 gene expression per se. Defects
in RT6 gene regulation or other cellular defects leading to premature cell
death in the T-cell lineage, alone or in combination, may instead be
responsible.
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Copyright © 1993 by the American Diabetes Association.
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