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Original Articles

Islet-Specific T-Cell Clones From the NOD Mouse Respond to β-Granule Antigen

  1. Barbara Bergman and
  2. Kathrin Haskins
  1. Barbara Davis Center for Childhood Diabetes and the Department of Immunology, University of Colorado Health Sciences Center Denver, Colorado
  1. Address correspondence and reprint requests to Dr. Kathryn Haskins, Barbara Davis Center for Childhood Diabetes and the Department of Immunology, University of Colorado Health Sciences Center, 4200 East 9th Avenue, Box BI40, Denver, CO 80262.
Diabetes 1994 Feb; 43(2): 197-203. https://doi.org/10.2337/diab.43.2.197
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Abstract

Islet-reactive T-cell clones from NOD mice provide an important approach to the investigation of antigens with relevance to type I diabetes. To identify a source of β-cell antigen suitable for biochemical studies, we have used two islet-specific, diabetogenic T-cell clones to test β-tumor cells. β-tumor cell lines, maintained in continuous culture, were found to lose antigenicity rapidly. However, cells harvested directly from β-tumors arising spontaneously in the transgenic NOD/Lt-Tg(RIPTag)1Lt mouse proved to be a potent source of β-cell antigen for the T-cell clones. Subcellular fractionation of β-tumor cells showed that the T-cell antigen was highly enriched in the β-granule fraction and that this activity was associated with the granule membrane.

  • Received July 26, 1993.
  • Revision received October 5, 1993.
  • Accepted October 5, 1993.
  • Copyright © 1994 by the American Diabetes Association
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February 1994, 43(2)
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Islet-Specific T-Cell Clones From the NOD Mouse Respond to β-Granule Antigen
Barbara Bergman, Kathrin Haskins
Diabetes Feb 1994, 43 (2) 197-203; DOI: 10.2337/diab.43.2.197

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Islet-Specific T-Cell Clones From the NOD Mouse Respond to β-Granule Antigen
Barbara Bergman, Kathrin Haskins
Diabetes Feb 1994, 43 (2) 197-203; DOI: 10.2337/diab.43.2.197
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