miR-381 modulates human bone mesenchymal stromal cells (BMSCs) osteogenesis via suppressing Wnt signaling pathway during atrophic nonunion development

Cell Death Dis. 2019 Jun 17;10(7):470. doi: 10.1038/s41419-019-1693-z.

Abstract

The osteogenic differentiation of human bone mesenchymal stromal cells (BMSCs) has been considered as a central issue in fracture healing. Wnt signaling could promote BMSC osteogenic differentiation through inhibiting PPARγ. During atrophic nonunion, Wnt signaling-related factors, WNT5A and FZD3 proteins, were significantly reduced, along with downregulation of Runx2, ALP, and Collagen I and upregulation of PPARγ. Here, we performed a microarray analysis to identify differentially expressed miRNAs in atrophic nonunion tissues that were associated with Wnt signaling through targeting related factors. Of upregulated miRNAs, miR-381 overexpression could significantly inhibit the osteogenic differentiation in primary human BMSCs while increase in PPARγ protein level. Through binding to the 3'UTR of WNT5A and FZD3, miR-381 modulated the osteogenic differentiation via regulating β-catenin nucleus translocation. Moreover, PPARγ, an essential transcription factor inhibiting osteogenic differentiation, could bind to the promoter region of miR-381 to activate its expression. Taken together, PPARγ-induced miR-381 upregulation inhibits the osteogenic differentiation in human BMSCs through miR-381 downstream targets, WNT5A and FZD3, and β-catenin nucleus translocation in Wnt signaling. The in vivo study also proved that inhibition of miR-381 promoted the fracture healing. Our finding may provide a novel direction for atrophic nonunion treatment.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Animals
  • Atrophy
  • Base Sequence
  • Cell Differentiation / genetics
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Down-Regulation / genetics
  • Femoral Fractures / genetics
  • Fracture Healing / genetics
  • Fractures, Ununited / genetics*
  • Fractures, Ununited / pathology*
  • Humans
  • Male
  • Mesenchymal Stem Cells / metabolism*
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Osteoblasts / metabolism
  • Osteogenesis* / genetics
  • PPAR gamma / metabolism
  • Promoter Regions, Genetic / genetics
  • Protein Binding
  • Protein Transport
  • Rats, Sprague-Dawley
  • Wnt Signaling Pathway* / genetics
  • beta Catenin / metabolism

Substances

  • MIRN381 microRNA, human
  • MicroRNAs
  • PPAR gamma
  • beta Catenin