By inhibiting ADCY5, miR-18a-3p promotes osteoporosis and possibly contributes to spinal fracture

Biochem Biophys Res Commun. 2021 Apr 23:550:49-55. doi: 10.1016/j.bbrc.2021.02.118. Epub 2021 Mar 5.

Abstract

To investigate the influence of miR-18a-3p and ADCY5 on OP and osteogenic differentiation of human Mesenchymal stem cell (hBMSCs) and its possible mechanism. Samples were collected from osteoporotic patients with or without vertebral compression fracture, and without OP volunteers. MiR-18a-3p and ADCY5 mRNA expression levels in the tissue samples and hBMSCs during osteogenic differentiation were detected。MiR-18a-3p mimic and OE-ADCY5 were introduced into hBMSCs to research the effects of miR-18a-3p and ADCY5 on osteogenesis differentiation of hBMSCs. Dual luciferase reporter system and RNA pull-down were applied to determine whether ADCY5 was a target gene of miR-18a-3p. Compared with the control group, ADCY5 expression level was down-regulated in patients with OP-no-Frx and OP-Frx, but that of miR-18a-3p was up-regulated. In addition, ADCY5 increased during osteogenesis differentiation of hBMSCs, whereas miR-18a-3p did not. OE-ADCY5 significantly facilitated calcium deposition, ALP activity, osteoblast protein expression (OSX, ALP and EUNX2), miR-18a-3p mimic inhibited osteogenic differentiation, and partially reversed the effect of OE-ADCY5 on osteogenic differentiation. In general, miR-18a-3p targets ADCY5 to promote OP and may be involved in spinal fracturs.

Keywords: ADCY5; Human mesenchymal stem cells; MiR-18a-3p; Osteogenic differentiation; Osteoporosis; Spinal fracture.

MeSH terms

  • Adenylyl Cyclases / deficiency*
  • Adenylyl Cyclases / genetics*
  • Base Sequence
  • Calcium / metabolism
  • Genes, Reporter
  • Humans
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism
  • MicroRNAs / genetics*
  • Osteoblasts / cytology
  • Osteoblasts / metabolism
  • Osteogenesis / genetics*
  • Osteoporosis / genetics*
  • Osteoporosis / pathology*
  • Spinal Fractures / genetics*
  • Spinal Fractures / pathology

Substances

  • MIRN18A microRNA, human
  • MicroRNAs
  • Adenylyl Cyclases
  • adenylyl cyclase type V
  • Calcium