Determination of Glutamic Acid Decarboxylase (GAD65) in Pancreatic Islets and ItsIn VitroandIn VivoDegradation Kinetics in Serum Using a Highly Sensitive Enzyme Immunoassay

Author:

Schlosser Michael12,Walschus Uwe12,Klöting Ingrid3,Walther Reinhard1

Affiliation:

1. Department of Medical Biochemistry and Molecular Biology, Ernst Moritz Arndt University of Greifswald, Karlsburg, Germany

2. Institute of Pathophysiology, Ernst Moritz Arndt University of Greifswald, Karlsburg, Germany

3. Department of Laboratory Animal Science, Ernst Moritz Arndt University of Greifswald, Karlsburg, Germany

Abstract

Glutamic acid decarboxylase GAD65 autoantibodies (GADA) are an established marker for autoimmune diabetes. Recently, the autoantigen GAD65 itself was proposed as biomarker of beta-cell loss for prediction of autoimmune diabetes and graft rejection after islet transplantation. Therefore, the GAD65 content in pancreatic islets of different species and its serum degradation kinetics were examined in this study using a sensitive immunoassay. GAD65 was found in quantities of 78 (human), 43.7 (LEW.1A rat) and 37.4 (BB/OK rat) ng per 1,000 islets, respectively, but not in mouse islets. Thein vitrohalf-life of porcine GAD65 and human recombinant GAD65 ranged from 1.27 to 2.35 hours at 37°C in human serum, plasma and blood, and was unaffected by presence of GAD65 autoantibodies. After injecting 2,000 ng recombinant human GAD65 into LEW.1A rats, thein vivohalf-life was 2.77 hours. GAD65 was undetectable after 24 hours in these animals, and for up to 48 hours following diabetes induction by streptozotocin in LEW.1A rats. Estimated from these data, at least 13 islets in rat and 1,875 in human must be simultaneously destroyed to detect GAD65 in circulation. These results should be taken into consideration in further studies aimed at examining the diagnostic relevance of GAD65.

Publisher

Hindawi Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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