MiR-6869-5p Induces M2 Polarization by Regulating PTPRO in Gestational Diabetes Mellitus

Mediators Inflamm. 2021 Apr 30:2021:6696636. doi: 10.1155/2021/6696636. eCollection 2021.

Abstract

The role of microRNA (miRNA) in gestational diabetes mellitus has been widely investigated during the last decade. However, the altering effect of miR-6869-5p on immunity and placental microenvironment in gestational diabetes mellitus is largely unknown. In our study, the expression of miR-6869-5p was documented to be significantly decreased in placenta-derived mononuclear macrophages, which was also negatively related to PTPRO. Besides, PTPRO was negatively regulated by miR-6869-5p in placenta-derived mononuclear macrophages. In vitro, miR-6869-5p inhibited macrophage proliferation demonstrated by EdU and CCK-8 experiments. The inflammatory response in macrophages was also significantly inhibited by miR-6869-5p, which could regulate PTPRO as a target documented by luciferase reporter assay. Moreover, miR-6869-5p promoted M2 macrophage polarization and thus restrain inflammation. Accordingly, miR-6869-5p is involved in maintaining placental microenvironment balance by preventing from inflammation and inducing M2 macrophages in gestational diabetes mellitus.

MeSH terms

  • Diabetes, Gestational* / genetics
  • Diabetes, Gestational* / metabolism
  • Female
  • Humans
  • Macrophage Activation
  • Macrophages / metabolism
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Placenta / metabolism
  • Pregnancy
  • Receptor-Like Protein Tyrosine Phosphatases, Class 3 / metabolism

Substances

  • MIRN6869 microRNA, human
  • MicroRNAs
  • PTPRO protein, human
  • Receptor-Like Protein Tyrosine Phosphatases, Class 3