GAD is an autoantigen in IDDM. Molecular cloning and specific antibodies allowed us to demonstrate that only the lower Mr GAD64 isoform is expressed in human islets, in contrast to human brain, rat islets, and rat brain, all of which express both GAD64 and GAD67. Expression of the human islet GAD64 isoform in COS-7 and BHK cells resulted in an enzymatically active rGAD64, which is immunoreactive with diabetic sera comparable with that of the islet 64,000-Mr autoantigen. Immunoprecipitation analyses showed that 21/28 (75%) IDDM sera had rGAD64 antibodies compared with only 1/59 (1.7%) of the healthy control sera. In immunoblot analyses, an SMS serum—but only 1/10 randomly selected IDDM sera—recognized the blotted rGAD64 without relation to immunoprecipitation titers. In conclusion, only the GAD64 isoform is expressed in human islets, in contrast to rat islets, which also express the GAD67 isoform. The immunological properties of human rGAD64 are comparable with the native 64,000-Mr islet autoantigen, allowing further studies of the immunopathogenesis of IDDM.
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October 01 1992
Recombinant Glutamic Acid Decarboxylase (Representing the Single Isoform Expressed in Human Islets) Detects IDDM-Associated 64,000-Mr Autoantibodies
Allan E Karlsen;
Allan E Karlsen
Department of Endocrinology, Karolinska Hospital
Stockholm, Sweden
The Hagedorn Research Institute
Gentofte, Denmark
The R.H. Williams Laboratory, Department of Medicine, University of Washington
Seattle
Bioscience and Diabetes Research, Novo Nordisk A/S
Bagsvaerd, Denmark
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William A Hagopian;
William A Hagopian
Department of Endocrinology, Karolinska Hospital
Stockholm, Sweden
The Hagedorn Research Institute
Gentofte, Denmark
The R.H. Williams Laboratory, Department of Medicine, University of Washington
Seattle
Bioscience and Diabetes Research, Novo Nordisk A/S
Bagsvaerd, Denmark
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Jacob S Petersen;
Jacob S Petersen
Department of Endocrinology, Karolinska Hospital
Stockholm, Sweden
The Hagedorn Research Institute
Gentofte, Denmark
The R.H. Williams Laboratory, Department of Medicine, University of Washington
Seattle
Bioscience and Diabetes Research, Novo Nordisk A/S
Bagsvaerd, Denmark
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Esper Boel;
Esper Boel
Department of Endocrinology, Karolinska Hospital
Stockholm, Sweden
The Hagedorn Research Institute
Gentofte, Denmark
The R.H. Williams Laboratory, Department of Medicine, University of Washington
Seattle
Bioscience and Diabetes Research, Novo Nordisk A/S
Bagsvaerd, Denmark
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Thomas Dyrberg;
Thomas Dyrberg
Department of Endocrinology, Karolinska Hospital
Stockholm, Sweden
The Hagedorn Research Institute
Gentofte, Denmark
The R.H. Williams Laboratory, Department of Medicine, University of Washington
Seattle
Bioscience and Diabetes Research, Novo Nordisk A/S
Bagsvaerd, Denmark
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Catherine E Grubin;
Catherine E Grubin
Department of Endocrinology, Karolinska Hospital
Stockholm, Sweden
The Hagedorn Research Institute
Gentofte, Denmark
The R.H. Williams Laboratory, Department of Medicine, University of Washington
Seattle
Bioscience and Diabetes Research, Novo Nordisk A/S
Bagsvaerd, Denmark
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Birgitte K Michelsen;
Birgitte K Michelsen
Department of Endocrinology, Karolinska Hospital
Stockholm, Sweden
The Hagedorn Research Institute
Gentofte, Denmark
The R.H. Williams Laboratory, Department of Medicine, University of Washington
Seattle
Bioscience and Diabetes Research, Novo Nordisk A/S
Bagsvaerd, Denmark
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Ole D Madsen;
Ole D Madsen
Department of Endocrinology, Karolinska Hospital
Stockholm, Sweden
The Hagedorn Research Institute
Gentofte, Denmark
The R.H. Williams Laboratory, Department of Medicine, University of Washington
Seattle
Bioscience and Diabetes Research, Novo Nordisk A/S
Bagsvaerd, Denmark
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Åke Lernmark
Åke Lernmark
Department of Endocrinology, Karolinska Hospital
Stockholm, Sweden
The Hagedorn Research Institute
Gentofte, Denmark
The R.H. Williams Laboratory, Department of Medicine, University of Washington
Seattle
Bioscience and Diabetes Research, Novo Nordisk A/S
Bagsvaerd, Denmark
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Please address correspondence and reprint requests to Allan E. Karlsen, The Hagedorn Research Institute, Niels Steensens Vej 6, DK-2820 Gentofte, Denmark.
Diabetes 1992;41(10):1355–1359
Article history
Received:
May 08 1992
Revision Received:
July 09 1992
Accepted:
July 09 1992
PubMed:
1397711
Citation
Allan E Karlsen, William A Hagopian, Jacob S Petersen, Esper Boel, Thomas Dyrberg, Catherine E Grubin, Birgitte K Michelsen, Ole D Madsen, Åke Lernmark; Recombinant Glutamic Acid Decarboxylase (Representing the Single Isoform Expressed in Human Islets) Detects IDDM-Associated 64,000-Mr Autoantibodies. Diabetes 1 October 1992; 41 (10): 1355–1359. https://doi.org/10.2337/diab.41.10.1355
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