Glucolipotoxicity-Inhibited Regulates Pancreatic β-Cell Function and Survival.

Inhibition of microRNAs (miRNAs) essential for pancreatic β-cell biology (e.g., ) results in β-cell failure and diabetes in rodent models. Whether the downregulation of miRNAs in pancreatic islets is involved in the development of human type 2 diabetes remains unclear. Here, utilizing a miRNA microarray, we identified a set of miRNAs that were differentially expressed in healthy human islets under glucolipotoxic conditions. A downregulated miRNA, , was preferentially studied since its inhibition caused dramatic β-cell dysfunction and apoptosis. Proteomic profiling and bioinformatics methods identified four target genes, including a Trp53 effector, , that were further confirmed by luciferase reporter assays. We narrowed down the effector of downregulation to PERP owing to its upregulation in islets from diabetic rodents. Indeed, inhibition prevented the β-cell impairment caused by either reduction or glucolipotoxicity. Further investigations confirmed the modulatory effect of PERP on insulin secretion. Collectively, appears to be an essential regulator of β-cell biology, and its downregulation links PERP enhancement to β-cell dysfunction and apoptosis in glucolipotoxic settings. Our work demonstrates a novel mechanism of glucolipotoxicity-induced β-cell failure mediated via downregulation.