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1型糖尿病模型中的母体因素对后代胰岛炎和显性糖尿病的发展有不同影响。

Maternal factors in a model of type 1 diabetes differentially affect the development of insulitis and overt diabetes in offspring.

作者信息

Kagohashi Yukiko, Udagawa Jun, Abiru Norio, Kobayashi Masakazu, Moriyama Kenji, Otani Hiroki

机构信息

Department of Developmental Biology, Faculty of Medicine, Shimane University, Izumo, Shimane, 693-8501, Japan.

出版信息

Diabetes. 2005 Jul;54(7):2026-31. doi: 10.2337/diabetes.54.7.2026.

Abstract

Type 1 diabetes, a multifactorial disease involving genetic and environmental factors, results from the destruction of pancreatic beta-cells. The maternal environment has been suggested to be important in the development of diabetes. To assess the role of maternal factors in the development of insulitis and overt diabetes, we transplanted pre-implantation stage embryos of nonobese diabetic (NOD) mice, a model of type 1 diabetes, into the uterus of each recipient. Recipients were ICR and DBA/2J mice without diabetic genetic predisposition and NOD mice not exhibiting overt diabetes during the experiment; offspring were designated as NOD/ICR, NOD/DBA, and NOD/NOD, respectively; unmanipulated NOD offspring were also examined. NOD/ICR and NOD/DBA offspring developed insulitis significantly earlier than NOD/NOD offspring. However, overt diabetes was significantly suppressed in NOD/ICR and NOD/DBA offspring in comparison with NOD/NOD offspring. Insulin autoantibodies (IAAs) were undetectable in ICR and DBA/2J surrogate mothers and in NOD/ICR and NOD/DBA offspring at the onset of insulitis, suggesting that maternal factors other than transmitted IAAs induced the earlier onset. The present study indicates that altered maternal factors modify the immune response to islets, which in turn might affect the pathogenic course from insulitis to overt diabetes.

摘要

1型糖尿病是一种涉及遗传和环境因素的多因素疾病,由胰腺β细胞的破坏引起。母体环境被认为在糖尿病的发生发展中很重要。为了评估母体因素在胰岛炎和显性糖尿病发生中的作用,我们将1型糖尿病模型非肥胖糖尿病(NOD)小鼠的植入前阶段胚胎移植到每个受体的子宫中。受体为无糖尿病遗传易感性的ICR和DBA/2J小鼠以及在实验期间未表现出显性糖尿病的NOD小鼠;后代分别被指定为NOD/ICR、NOD/DBA和NOD/NOD;未进行处理的NOD后代也进行了检查。NOD/ICR和NOD/DBA后代发生胰岛炎的时间明显早于NOD/NOD后代。然而,与NOD/NOD后代相比,NOD/ICR和NOD/DBA后代的显性糖尿病明显受到抑制。在胰岛炎发作时,ICR和DBA/2J代孕母亲以及NOD/ICR和NOD/DBA后代中均未检测到胰岛素自身抗体(IAA),这表明除了传递的IAA之外的母体因素诱导了更早的发病。本研究表明,母体因素的改变会改变对胰岛的免疫反应,进而可能影响从胰岛炎到显性糖尿病的致病过程。

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