首页> 外文期刊>Diabetes >β-Cell Destruction in NOD Mice Correlates With Fas (CD95) Expression on β-Cells and Proinflammatory Cytokine Expression in Islets
【24h】

β-Cell Destruction in NOD Mice Correlates With Fas (CD95) Expression on β-Cells and Proinflammatory Cytokine Expression in Islets

机译:NOD小鼠的β细胞破坏与胰岛Fas(CD95)表达和胰岛促炎细胞因子表达相关

获取原文
获取原文并翻译 | 示例
       

摘要

A mechanism of autoimmune destruction of islet β-cells in type 1 diabetes has been proposed to be the binding of Fas ligand (FasL) on T-cells to Fas receptors on β-cells. We investigated this proposal by examining the expression of FasL and Fas on islet-infiltrating T-cells and β-cells in relation to β-cell destruction in a syn- geneic islet transplant model in NOD mice. Diabetic NOD mice were transplanted with syngeneic islets and Injected with complete Freund's adjuvant, which pre- Vented diabetes recurrence (nondestructive insulitis), And with phosphate-buffered saline, which did not (β-cell Destructive insulitis).
机译:有人提出在1型糖尿病中自身免疫破坏胰岛β细胞的机制是T细胞上的Fas配体(FasL)与β细胞上的Fas受体结合。我们通过研究NOD小鼠同基因胰岛移植模型中与胰岛浸润性T细胞和β细胞上FasL和Fas的表达有关的β细胞破坏,研究了这一提议。糖尿病NOD小鼠移植了同基因胰岛,并注射了完全的弗氏佐剂,可以预防糖尿病复发(非破坏性胰岛炎),而磷酸盐缓冲液则不能(β细胞破坏性胰岛炎)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号