CRTC2 suppresses BMP2-induced osteoblastic differentiation via Smurf1 expression in MC3T3-E1 cells

Life Sci. 2018 Dec 1:214:70-76. doi: 10.1016/j.lfs.2018.10.052. Epub 2018 Oct 26.

Abstract

Aims: CREB (cAMP response element-binding protein)-regulated transcription coactivator (CRTC2) has been reported to act as a coactivator of CREB during gluconeogenesis. The role of CRTC2 in osteoblastic differentiation has not yet been elucidated. The aim of this study is to identify the mechanism of CRTC2 in osteoblast differentiation.

Main methods: The mRNA expression was determined by RT-PCR and qPCR. Protein levels were measured using Western blot assay. Alkaline phosphatase (ALP) staining was performed to evaluate ALP activity. Alizarin red S (ARS) staining was performed to measure extracellular mineralization. Transcriptional activity was detected using a luciferase assay.

Key findings: In the present study, TNF-α was found to stimulate CRTC2 expression. However, TNF-α did not increase the gene expression of osteoblast differentiation markers and inhibited BMP2-induced osteoblastic differentiation. Overexpression of CRTC2 decreased the expression of osteogenic genes, ALP activity and extracellular matrix mineralization. Knockdown of CRTC2 restored BMP2-induced osteogenic gene expression and ALP activity. CRTC2 increased Smurf1 mRNA expression, Smurf 1 promoter activity, and protein level. Furthermore, Smurf 1 decreased Smad 1/5/9 protein levels. These results suggest that CRTC2 decreased BMP2-induced osteoblastic differentiation via Smurf 1 expression.

Significance: Our results indicate that CRTC2 regulates the expression of Smurf1 in osteoblast differentiation.

Keywords: BMP2; CRTC2; Osteoblast; Smad; Smurf1; TNF-α.

MeSH terms

  • Animals
  • Bone Morphogenetic Protein 2 / genetics
  • Bone Morphogenetic Protein 2 / pharmacology
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Cell Line
  • Gene Silencing
  • Mice
  • Osteoblasts / cytology*
  • Osteoblasts / drug effects
  • Osteoblasts / physiology
  • Recombinant Proteins / genetics
  • Recombinant Proteins / pharmacology
  • Smad1 Protein / genetics
  • Smad1 Protein / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Tumor Necrosis Factor-alpha / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism*

Substances

  • Bone Morphogenetic Protein 2
  • Crtc2 protein, mouse
  • Recombinant Proteins
  • Smad1 Protein
  • Smad1 protein, mouse
  • Transcription Factors
  • Tumor Necrosis Factor-alpha
  • Smurf1 protein, mouse
  • Ubiquitin-Protein Ligases