Circulating microRNA-375 as biomarker of pancreatic beta cell death and protection of beta cell mass by cytoprotective compounds

PLoS One. 2017 Oct 17;12(10):e0186480. doi: 10.1371/journal.pone.0186480. eCollection 2017.

Abstract

Objective: Previous studies demonstrated that circulating microRNA-375 (miR-375) is a suitable plasma biomarker for real-time detection of beta cell death. The present study evaluated the use of this biomarker to assess the beta cytoprotective effect of phenylpropenoic acid glucoside (PPAG), which was previously demonstrated to protect beta cells against various types of injury, and of exendin-4, which is an established antidiabetic drug.

Methods: PPAG or exendin-4 were administered in mice treated with streptozotocin (STZ) to acutely induce beta cell death. Beta cell mass and apoptotic death were measured in pancreatic tissue sections. Circulating miR-375 was measured in blood plasma by RT-qPCR. The release of miR-375 was also measured in vitro by MIN-6 beta cells.

Results: Administration of STZ resulted in measurable circulating levels of miR-375, a decrease in beta cell mass and increase in frequency of apoptotic beta cells. In vitro, there was a good correlation between miR-375 release and the extent of beta cell death. Treatment of mice with PPAG or exendin-4 significantly attenuated STZ-induced loss of beta cell mass and beta cell apoptosis, and normalized the blood level of miR-375.

Conclusions: These findings show the potential use of serological miR-375 measurements to evaluate the beta cytoprotective effect of (potential) antidiabetic drugs in vivo.

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Biomarkers / blood
  • Blood Glucose / drug effects
  • Blood Glucose / metabolism
  • Cell Line
  • Diabetes Mellitus, Experimental / blood*
  • Diabetes Mellitus, Experimental / chemically induced
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / genetics
  • Exenatide
  • Glucosides / pharmacology*
  • Hypoglycemic Agents / pharmacology*
  • Insulin-Secreting Cells / drug effects
  • Insulin-Secreting Cells / metabolism*
  • Insulin-Secreting Cells / pathology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • MicroRNAs / blood
  • MicroRNAs / genetics*
  • Pancreas / drug effects
  • Pancreas / metabolism
  • Pancreas / pathology
  • Peptides / pharmacology
  • Phenylpropionates / pharmacology*
  • Protective Agents / pharmacology
  • Streptozocin
  • Venoms / pharmacology

Substances

  • 2-(glucopyranosyloxy)-3-phenylpropenoic acid
  • Biomarkers
  • Blood Glucose
  • Glucosides
  • Hypoglycemic Agents
  • MicroRNAs
  • Mirn375 microRNA, mouse
  • Peptides
  • Phenylpropionates
  • Protective Agents
  • Venoms
  • Streptozocin
  • Exenatide

Grants and funding

This study was supported by research grants from the Research Foundation Flanders (FWO G.0492.12 project grant and Senior Clinical Investigator career support grant to G.A.M.), www.fwo.be; by the Agentschap voor Innovatie door Wetenschap en Technologie (IWT) with IWT-SB-141732 (to S.R and G.A.M.), https://www.iwt.be; by the Wetenschappelijk Fonds Willy Gepts from the Universitair Ziekenhuis Brussel (to G.A.M., S.R. and L.B.) and by the European Foundation for the Study of Diabetes (EFSD/JDRF/Lilly Programme 2015, to G.A.M.), www.europeandiabetesfoundation.org. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.