Circulating miR-375 as a Biomarker of β-Cell Death and Diabetes in Mice

被引:149
作者
Erener, Suheda [1 ]
Mojibian, Majid [1 ]
Fox, Jessica K. [1 ]
Denroche, Heather C. [1 ]
Kieffer, Timothy J. [1 ,2 ]
机构
[1] Univ British Columbia, Dept Cellular & Physiol Sci, Inst Life Sci, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Dept Surg, Inst Life Sci, Vancouver, BC V6T 1Z3, Canada
基金
加拿大自然科学与工程研究理事会; 瑞士国家科学基金会;
关键词
NOD MICE; TYPE-1; MICRORNAS; MECHANISM; APOPTOSIS; PLASMA; ALPHA; MOUSE; ONSET; MASS;
D O I
10.1210/en.2012-1744
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Type 1 diabetes is a progressive autoimmune disease that is largely silent in its initial stages. Yet, sensitive methods for detection of beta-cell death and prediction and prevention of diabetes are lacking. Micro-RNAs (miRNAs) have been found at high concentrations in body fluids. Here in this studywesought to determine whetheranislet enrichedmiRNA, miR-375, is a suitable blood marker to detect beta-cell death and predict diabetes in mice. We measured miR-375 levels by quantitative RT-PCR in plasma samples of streptozotocin (STZ)-treated C57BL/6 mice and nonobese diabetic (NOD) mice. We also measured miR-375 levels in media samples of cytokine- or STZ-treated islets in the presence or absence of cell-death inhibitors. High-dose STZ administration dramatically increased circulating miR-375 levels, prior to the onset of hyperglycemia. Similarly, in the NOD mouse model of autoimmune diabetes, circulating miR-375 levels were significantly increased 2 weeks before diabetes onset. Moreover, cytokine-and STZ-induced cell death in isolated mouse islets produced a striking increase in extracellular miR-375 levels, which was reduced by cell death inhibitors. These data suggest that circulating miR-375 can be used as a marker of beta-cell death and potential predictor of diabetes. (Endocrinology 154: 603-608, 2013)
引用
收藏
页码:603 / 608
页数:6
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