دورية أكاديمية

Liraglutide Enhances the Efficacy of Human Mesenchymal Stem Cells in Preserving Islet ß-cell Function in Severe Non-obese Diabetic Mice

التفاصيل البيبلوغرافية
العنوان: Liraglutide Enhances the Efficacy of Human Mesenchymal Stem Cells in Preserving Islet ß-cell Function in Severe Non-obese Diabetic Mice
المؤلفون: Li-rong Li, Jing Lu, Xiao-lei Jia, Hui Hui, Jie Zhang, Ying Liu, Wei-juan Cui, Qian-yue Xu, Da-long Zhu
المصدر: Molecular Medicine, Vol 22, Iss 1, Pp 800-808 (2016)
بيانات النشر: BMC, 2016.
سنة النشر: 2016
المجموعة: LCC:Therapeutics. Pharmacology
LCC:Biochemistry
مصطلحات موضوعية: Therapeutics. Pharmacology, RM1-950, Biochemistry, QD415-436
الوصف: Abstract Glucagon-like peptide 1 (GLP-1) can promote islet β cell replication and function, and mesenchymal stem cells (MSCs) can inhibit T cell autoimmunity. The aim of this study was to test the dynamic distribution of infused human MSCs and the therapeutic effect of combined MSCs and liraglutide, a long-acting GLP-1 analog, on preserving β cell function in severe nonobese diabetic (NOD) mice. We found that infused MSCs accumulated in the pancreas at 4 wks post infusion, which was not affected by liraglutide treatment. Liraglutide significantly enhanced the function of MSCs to preserve islet β cells by reducing glucose levels 30 min post glucose challenge and increasing the content and secretion of insulin by islet β cells in severely diabetic mice. Infusion with MSCs significantly reduced insulitis scores but increased the frequency of splenic Tregs, accompanied by a reduction in plasma IFN-γ and TNF-α levels and an elevation of plasma IL-10 and transforming growth factor-β1 (TGF-β1) levels in NOD mice. Although liraglutide mitigated MSC-mediated changes in the frequency of Tregs and the level of plasma IL-10, it significantly increased the plasma TGF-β1 levels in severely diabetic mice. Therefore, our findings suggest that liraglutide could enhance the therapeutic efficacy of MSCs in the treatment of severe type 1 diabetes.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1076-1551
1528-3658
Relation: http://link.springer.com/article/10.2119/molmed.2016.00168; https://doaj.org/toc/1076-1551; https://doaj.org/toc/1528-3658
DOI: 10.2119/molmed.2016.00168
URL الوصول: https://doaj.org/article/d78e06c1741c49349318542098f9d542
رقم الأكسشن: edsdoj.78e06c1741c49349318542098f9d542
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:10761551
15283658
DOI:10.2119/molmed.2016.00168