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首页> 外文期刊>Disease markers >Determination of glutamic acid decarboxylase (GAD65) in pancreatic islets and its in vitro and in vivo degradation kinetics in serum using a highly sensitive enzyme immunoassay
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Determination of glutamic acid decarboxylase (GAD65) in pancreatic islets and its in vitro and in vivo degradation kinetics in serum using a highly sensitive enzyme immunoassay

机译:使用高灵敏度酶免疫法测定胰岛中的谷氨酸脱羧酶(GAD65)及其在血清中的体内和体外降解动力学

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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. The in vitro half-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, the in vivo half-life was 2.77 hours. GAD65 was undetectable after 24 hours in these animals, and for up to 48 hours following diabetes induction by streptozotocinin LEW.lArats. 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.
机译:谷氨酸脱羧酶GAD65自身抗体(GADA)是自身免疫性糖尿病的公认标志物。最近,提出了自身抗原GAD65本身作为β细胞损失的生物标志物,用于预测自身免疫性糖尿病和胰岛移植后移植排斥。因此,本研究使用敏感的免疫分析方法检测了不同物种的胰岛中GAD65的含量及其血清降解动力学。每1,000个胰岛中发现GAD65的量分别为78(人类),43.7(LEW.1A大鼠)和37.4(BB / OK大鼠)ng,但在小鼠胰岛中没有。猪GAD65和人重组GAD65在37?C的体外半衰期为1.27至2.35小时。人血清,血浆和血液中的C,并且不受GAD65自身抗体的影响。向LEW.1A大鼠中注射2,000 ng重组人GAD65后,体内半衰期为2.77小时。在这些动物中24小时后以及链脲佐菌素LEW.1Arat诱导糖尿病后长达48小时,GAD65均未检出。根据这些数据估算,必须同时破坏大鼠中的至少13个胰岛和人中的1875个胰岛,以检测循环中的GAD65。在旨在检查GAD65诊断相关性的进一步研究中应考虑这些结果。

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