Icariin stimulates osteogenic differentiation of rat bone marrow stromal stem cells by increasing TAZ expression

Biomed Pharmacother. 2017 Jul:91:581-589. doi: 10.1016/j.biopha.2017.04.019. Epub 2017 May 6.

Abstract

Icariin, the major ingredient of Herba Epimedii, promotes the osteogenic differentiation of rat bone marrow stromal cells (rBMSCs) and exerts protective effects against bone loss and increases bone regeneration, but the underlying signaling pathway by which icariin affects osteogenic differentiation remain unclear. Transcriptional coactivator with PDZ-binding motif (TAZ) is a transcriptional modulator of the Hippo signaling pathway, which plays an important role in the osteogenic differentiation of BMSCs by activating Runx2 gene during the terminal osteogenic differentiation. In this study, we found that 0.1μM icariin markedly promoted the proliferation, calcium depositions, and osteogenic genes expression of rBMSCs. Icariin (0.1μM) upregulated TAZ, Runx2, β-catenin, Osteopotin, and Dlx5 expression mainly at the early stage of osteogenic differentiation, and increased osteocalcin expression at the late stage. Our result further demonstrated that knockdown TAZ expression by lentivirus-mediated TAZ shRNA inhibited the icariin-induced osteogenic differentiation. Moreover, ICI 182780 (the estrogen receptor alpha inhibitor) or DKK1 (the Wnt/β-catenin pathway inhibitor), inhibited the icariin-induced increase in TAZ expression. Furthermore, icariin stimulated the activation of TAZ as evidenced by increased total TAZ protein and nuclear translocation, but these effects of icariin were blocked by ICI 182780 or DKK1. Taken together, our results demonstrate that icariin promotes the osteogenic differentiation of rBMSCs by increasing TAZ expression, and that the increased TAZ expression induced by icariin is mostly mediated by the ERα and Wnt/β-catenin pathway.

Keywords: Bone marrow stromal cells; Icariin; Osteogenic differentiation; Transcriptional coactivator with PDZ-binding motif.

MeSH terms

  • Animals
  • Cell Differentiation / drug effects*
  • Cell Differentiation / genetics
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Cell Proliferation / drug effects
  • Cell Shape / drug effects
  • Estradiol / analogs & derivatives
  • Estradiol / pharmacology
  • Estrogen Receptor alpha / metabolism
  • Flavonoids / pharmacology*
  • Fulvestrant
  • Gene Expression Regulation / drug effects
  • Gene Knockdown Techniques
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Lentivirus / metabolism
  • Male
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism*
  • Osteogenesis / drug effects*
  • Osteogenesis / genetics
  • Phenotype
  • Phosphorylation / drug effects
  • Protein Transport / drug effects
  • RNA, Small Interfering / metabolism
  • Rats, Sprague-Dawley
  • Transcriptional Coactivator with PDZ-Binding Motif Proteins
  • Wnt Signaling Pathway / drug effects

Substances

  • Dkk1 protein, rat
  • Estrogen Receptor alpha
  • Flavonoids
  • Intercellular Signaling Peptides and Proteins
  • Intracellular Signaling Peptides and Proteins
  • RNA, Small Interfering
  • Transcriptional Coactivator with PDZ-Binding Motif Proteins
  • WWTR1 protein, rat
  • Fulvestrant
  • Estradiol
  • icariin