MiR-637 maintains the balance between adipocytes and osteoblasts by directly targeting Osterix

Mol Biol Cell. 2011 Nov;22(21):3955-61. doi: 10.1091/mbc.E11-04-0356. Epub 2011 Aug 31.

Abstract

Bone development is dynamically regulated by homeostasis, in which a balance between adipocytes and osteoblasts is maintained. Disruption of this differentiation balance leads to various bone-related metabolic diseases, including osteoporosis. In the present study, a primate-specific microRNA (miR-637) was found to be involved in the differentiation of human mesenchymal stem cells (hMSCs). Our preliminary data indicated that miR-637 suppressed the growth of hMSCs and induced S-phase arrest. Expression of miR-637 was increased during adipocyte differentiation (AD), whereas it was decreased during osteoblast differentiation (OS), which suggests miR-637 could act as a mediator of adipoosteogenic differentiation. Osterix (Osx), a significant transcription factor of osteoblasts, was shown to be a direct target of miR-637, which significantly enhanced AD and suppressed OS in hMSCs through direct suppression of Osx expression. Furthermore, miR-637 also significantly enhanced de novo adipogenesis in nude mice. In conclusion, our data indicated that the expression of miR-637 was indispensable for maintaining the balance of adipocytes and osteoblasts. Disruption of miR-637 expression patterns leads to irreversible damage to the balance of differentiation in bone marrow.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism
  • Adipocytes / physiology*
  • Adipogenesis / genetics
  • Adipose Tissue / anatomy & histology
  • Adipose Tissue / physiology
  • Adult
  • Alkaline Phosphatase / metabolism
  • Animals
  • Cell Cycle Checkpoints
  • Cell Proliferation
  • Cells, Cultured
  • Enzyme Assays
  • Female
  • Gene Expression
  • Gene Expression Regulation
  • Humans
  • Mesenchymal Stem Cells
  • Mice
  • Mice, Nude
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Middle Aged
  • Osteoblasts / metabolism
  • Osteoblasts / physiology*
  • Sp7 Transcription Factor
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • MIRN637 microRNA, human
  • MicroRNAs
  • Sp7 Transcription Factor
  • SP7 protein, human
  • Transcription Factors
  • Alkaline Phosphatase