Rat islets were mechanically dissociated to single cells and allowed to form aggregates by rotation-mediated cell-cell interaction. The aggregates, or neoislets, demonstrated insulin release in response to 20 mM glucose and 10 mM theophylline that was comparable to that of intact islets cultured for a similar time. However, basal insulin release was considerably greater than that from freshly isolated islets. The microscopic structure of the neoislets revealed sortinginto a B-cell domain at the surface with A-cells interior to the aggregate. The neoislets generated no mitogenic response in allogeneic lymph node lymphocytes. Reassociation of single islet cells provides stable, functional endocrine units with substantial reduction of immunogenicity.
Original Contribution|
September 01 1985
Structure, Function, and Immune Properties of Reassociated Islet Cells
Judith Shizuru;
Judith Shizuru
Department of Surgery, Stanford University School of Medicine
Stanford, California 94305
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David Trager;
David Trager
Department of Surgery, Stanford University School of Medicine
Stanford, California 94305
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Ronald C Merrell
Ronald C Merrell
Department of Surgery, Stanford University School of Medicine
Stanford, California 94305
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Address reprint requests to Ronald C. Merrell, M.D., The University of Texas Medical School at Houston, Department of Surgery, 6431 Fannin, Suite 4290, Houston, Texas 77030.
Diabetes 1985;34(9):898–903
Article history
Received:
October 05 1984
Revision Received:
March 12 1985
PubMed:
3161769
Citation
Judith Shizuru, David Trager, Ronald C Merrell; Structure, Function, and Immune Properties of Reassociated Islet Cells. Diabetes 1 September 1985; 34 (9): 898–903. https://doi.org/10.2337/diab.34.9.898
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