Hyperglycemia-induced changes in miRNA expression patterns in epicardial adipose tissue of piglets

J Endocrinol. 2016 Jun;229(3):259-66. doi: 10.1530/JOE-15-0495. Epub 2016 Apr 4.

Abstract

MicroRNAs (miRNAs) are a class of molecular posttranscriptional regulators found to participate in numerous biological mechanisms, such as adipogenesis, fat deposition, or glucose metabolism. Additionally, a detailed analysis on the molecular and cellular mechanisms of miRNA-related effects on metabolism leads to developing novel diagnostic markers and therapeutic approaches. To identify miRNA whose activity changed in epicardial adipose tissue in piglets during hyperglycemia, we analyzed the different miRNA expression patterns between control and hyperglycemia groups. The microarray analysis selected three differentially expressed microRNAs as potential biomarkers: hsa-miR-675-5p, ssc-miR-193a-3p, and hsa-miR-144-3p. The validation of miRNA expression with real-time PCR indicated an increased expression levels of ssc-miR-193a-3p and miR-675-5p, whereas the expression level of hsa-miR-144-3p was lower in epicardial adipose tissue in response to hyperglycemia (P<0.01). The Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses suggested that these miRNAs differentially expressed between hyperglycemic and control piglets are involved in insulin, adipocytokine, and phosphatidylinositol 3-kinase-Akt signaling pathways, and development of type 2 diabetes as well. The results suggested that hyperglycemia can significantly affect the expression patterns of miRNA in porcine adipose tissue.

Keywords: epicardial adipose tissue; hyperglycemia; miRNA; piglets.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Gene Expression Profiling
  • Genetic Markers
  • Glucose / metabolism
  • Hyperglycemia / blood
  • Hyperglycemia / genetics*
  • Hyperglycemia / metabolism
  • Insulin / metabolism
  • Insulin Resistance / genetics
  • Intra-Abdominal Fat / metabolism*
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Pericardium / metabolism*
  • Signal Transduction
  • Sus scrofa

Substances

  • Genetic Markers
  • Insulin
  • MicroRNAs
  • Glucose