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

Author:

Erener Suheda1,Mojibian Majid1,Fox Jessica K.1,Denroche Heather C.1,Kieffer Timothy J.2

Affiliation:

1. Departments of Cellular and Physiological Sciences (S.E., M.M., J.K.F., H.C.D., T.J.K.)Life Sciences Institute, University of British Columbia, V6T 1Z3 Vancouver, British Columbia, Canada

2. Surgery (T.J.K.), Life Sciences Institute, University of British Columbia, V6T 1Z3 Vancouver, British Columbia, Canada

Abstract

Type 1 diabetes is a progressive autoimmune disease that is largely silent in its initial stages. Yet, sensitive methods for detection of β-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 study we sought to determine whether an islet enriched miRNA, miR-375, is a suitable blood marker to detect β-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 β-cell death and potential predictor of diabetes.

Publisher

The Endocrine Society

Subject

Endocrinology

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