JACC Basic to Translational Science · 2018 · 57 citations · 40 references
MedicineCardiologyMolecular BiologyDiabetologyEpigeneticsGene ExpressionCardiovascular DiseaseDiabetes ManagementDiabetes MellitusIschemic Heart DiseaseMicrorna BiologyMicrorna-mediated RegulationCardiometabolic EpigeneticsExperimental ValidationMetabolic ModulationMicrorna Dysregulation In DiseaseMicrorna TherapeuticsMyocardial Ischemia-reperfusion InjuryMyocardial RepairO-glcnac Signaling
Management for patients with diabetes experiencing myocardial infarction remains a challenge. Here the authors show that hyperglycemia- and hyperinsulinemia-induced microRNA-24 (miR-24) reduction and O-GlcNAcylation in the diabetic heart contribute to poor survival and increased infarct size in diabetic myocardial ischemia/reperfusion (I/R). In a mouse model of myocardial I/R, pharmacological or genetic overexpression of miR-24 in hearts significantly reduced myocardial infarct size. Experimental validation revealed that miR-24 targets multiple key proteins, including O-GlcNac transferase, ATG4A, and BIM, to coordinately protect the myocardium from I/R injury. These results establish miR-24 as a promising therapeutic candidate for diabetic I/R injury.
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Medicine, Endocrinology, Physiology +14
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