miR-27a attenuates adipogenesis and promotes osteogenesis in steroid-induced rat BMSCs by targeting PPARγ and GREM1

Sci Rep. 2016 Dec 2:6:38491. doi: 10.1038/srep38491.

Abstract

The imbalance between adipogenic and osteogenic differentiation in bone marrow mesenchymal stem cells (BMSCs) plays a significant role in the pathogenesis of steroid-induced osteonecrosis of the femoral head (ONFH). Several microRNAs (miRNAs) are involved in regulating adipogenesis and osteogenesis. In this study, we established a steroid-induced ONFH rat model to identify the potential relevant miRNAs. We identified 9 up-regulated and 28 down-regulated miRNAs in the ONFH rat model. Of these, miR-27a was down-regulated and negatively correlated with peroxisome proliferator-activated receptor gamma (PPARγ) and gremlin 1 (GREM1) expression. Further studies confirmed that PPARγ and GREM1 were direct targets of miRNA-27a. Additionally, adipogenic differentiation was enhanced by miR-27a down-regulation, whereas miRNA-27a up-regulation attenuated adipogenesis and promoted osteogenesis in steroid-induced rat BMSCs. Moreover, miRNA-27a up-regulation had a stronger effect on adipogenic and osteogenic differentiation in steroid-induced rat BMSCs than si-PPARγ and si-GREM1. In conclusion, we identified 37 differentially expressed miRNAs in the steroid-induced ONFH model, of which miR-27a was down-regulated. Our results showed that miR-27a up-regulation could inhibit adipogenesis and promote osteogenesis by directly targeting PPARγ and GREM1. Thus, miR-27a is likely a key regulator of adipogenesis in steroid-induced BMSCs and a potential therapeutic target for ONFH treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics
  • Adipogenesis / drug effects
  • Adipogenesis / genetics*
  • Animals
  • Base Sequence
  • Cytokines
  • Disease Models, Animal
  • Down-Regulation / genetics
  • Female
  • Femur Head Necrosis / chemically induced
  • Femur Head Necrosis / genetics
  • Gene Expression Profiling
  • Male
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism*
  • MicroRNAs / metabolism*
  • Osteogenesis / drug effects
  • Osteogenesis / genetics*
  • PPAR gamma / metabolism*
  • Proteins / metabolism*
  • RNA, Small Interfering / metabolism
  • Rats, Sprague-Dawley
  • Steroids / adverse effects
  • Steroids / pharmacology*
  • Up-Regulation / genetics

Substances

  • 3' Untranslated Regions
  • Cytokines
  • Grem1 protein, rat
  • MIRN27 microRNA, rat
  • MicroRNAs
  • PPAR gamma
  • Proteins
  • RNA, Small Interfering
  • Steroids