MiR-5100 promotes osteogenic differentiation by targeting Tob2

J Bone Miner Metab. 2017 Nov;35(6):608-615. doi: 10.1007/s00774-016-0799-y. Epub 2016 Nov 21.

Abstract

MicroRNAs have emerged as pivotal regulators in various physiological and pathological processes, including osteogenesis. Here we discuss the contribution of miR-5100 to osteoblast differentiation and mineralization. We found that miR-5100 was upregulated during osteoblast differentiation in ST2 and MC3T3-E1 cells. Next, we verified that miR-5100 can promote osteogenic differentiation with gain-of-function and loss-of-function experiments. Target prediction analysis and experimental validation demonstrated that Tob2, which acts as a negative regulator of osteogenesis, was negatively regulated by miR-5100. Furthermore, we confirmed that the important bone-related transcription factor osterix, which can be degraded by binding to Tob2, was influenced by miR-5100 during osteoblast differentiation. Collectively, our results revealed a new molecular mechanism that fine-tunes osteoblast differentiation through miR-5100/Tob2/osterix networks.

Keywords: Mineralization; Osteoblast differentiation; Tob2; miR-5100.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Cycle Proteins / genetics*
  • Cell Cycle Proteins / metabolism
  • Cell Differentiation / genetics*
  • Cell Line
  • Gene Expression Regulation
  • Mice
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Osteoblasts / cytology
  • Osteoblasts / metabolism
  • Osteogenesis / genetics*
  • Sp7 Transcription Factor / genetics
  • Sp7 Transcription Factor / metabolism

Substances

  • Cell Cycle Proteins
  • MicroRNAs
  • Mirn5100 microRNA, mouse
  • Sp7 Transcription Factor
  • Sp7 protein, mouse
  • Tob2 protein, mouse