The proposal represents a continuation of our research in the area of islet cell culture and transplantation. The work is intended to serve as a basis for the eventual application of islet cell transplantation in Type 1 diabetes. Experiments within the proposal are directed toward the investigation of developing alternate methods for the acquisition of islet tissue. In addition, experiments involve the investigation of a unique method for the production of non-immunogenic islets which can be transplanted without immunosuppression between animals disparate at the major histocompatibility locus. Further understanding of the mechanism by which altered immunogenicity is attained is pursued. Methods for selective cell culture in which cells necessary for immune recognition can be controlled in vitro, are being explored. An experimental model of Type 1 diabetes as well as chemical forms of Type 1 diabetes are being examined to assess the utility of the technologies developed in the reversal of these hyperglycemic-insulinopenic syndromes. The approach centers on the acquisition of morphological data, coupled with biochemical and physiological studies. Technicques of immunoassay, morphometric analysis at the ultrastructural and light microscopical level, immunocytochemistry, spectrophotometry, chromatography, enzymology, tissue culture, transplantation permit the correlation of morphological, biochemical and physiological parameters. Major questions remain as barriers to human islet cell transplantation. Can efficient methods be developed for the isolation and purification of human islets? Can methods be developed permitting the purification of islet endocrine grafts circumventing rejection without the need for patient immunosuppression? Will the etiology of Type 1 diabetes be reexpressed in the transplanted grafts, compromising their function? It is hoped that experiments in this proposal will provide basic research which may lead to the answers to some of these questions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK032237-04
Application #
3230658
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Project Start
1983-04-01
Project End
1989-03-31
Budget Start
1986-04-01
Budget End
1987-03-31
Support Year
4
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Setum, C M; Serie, J R; Hegre, O D (1993) Dendritic cell/lymphocyte clustering: morphologic analysis by transmission electron microscopy and distribution of gold-labeled MHC class II antigens by high-resolution scanning electron microscopy. Anat Rec 235:285-95
Serie, J R; Pringle, J A; Cooper, H N et al. (1993) Long-term survival and strain-specific tolerance induction in rat-to-mouse neonatal islet xenografts. Transplantation 56:1166-70
Serie, J R; Pringle, J A; Cooper, H N et al. (1992) Tolerance induction in rat-to-mouse neonatal islet xenografts. Transplant Proc 24:644-6
Serie, J R; Cooper, H N; Kemmer, K A et al. (1992) Growth of neonatal islet transplants in the spontaneously diabetic BB/Wor rat. Diabetes 41:1122-9
Setum, C M; Serie, J R; Hegre, O D (1991) Comparative analysis of potency of splenic dendritic and adherent cells (macrophages) as alloantigen presenters in vivo. Diabetes 40:1719-24
Setum, C M; Serie, J R; Hegre, O D (1991) Confocal microscopic analysis of the nonendocrine cellular component of isolated adult rat islets of Langerhans. Transplantation 51:1131-3
Esteban, M M; Weinhaus, A J; Sueppel, K L et al. (1990) Effect of third-party, MHC-incompatible allograft rejection on cultured islet allografts. Transplant Proc 22:836-7
Hegre, O D; Serie, J R; Enriquez, A J et al. (1990) Growth of neonatal islet graft following transplantation to the BB/Wor rat. Horm Metab Res Suppl 25:142-7
Hegre, O D; Serie, J R; Weinhaus, A J et al. (1990) Cultured neonatal islet transplants in alloxan-treated and spontaneously diabetic rats. Horm Metab Res Suppl 25:108-16
Serie, J R; Goldberg, J E; Pringle, J A et al. (1990) Characterization of mononuclear infiltrates in rejecting and surviving murine islet allografts. Transplant Proc 22:814-5

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