共 23 条
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)
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页码:603 / 608
页数:6
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