Effect of bone morphogenic protein-7 on the expression of epithelial-mesenchymal transition markers in silicosis model

Exp Mol Pathol. 2015 Jun;98(3):393-402. doi: 10.1016/j.yexmp.2015.03.013. Epub 2015 Mar 12.

Abstract

This study presented the effect of bone morphogenic protein-7 (BMP-7) inhibiting epithelial-mesenchymal transition (EMT) in silicosis model. In vivo, Wistar rats were exposed to silica by intratracheal instillation. Seven days later rats were treated with BMP-7. Rats were sacrificed at 15 and 30days after exposure of silica. The results demonstrated vimentin expression was down-regulated; and E-cadherin was up-regulated after intervention with BMP-7. The TGF-β expression and phosphorylation-p38 were lower in BMP-7 treated group than in silica group. In vitro, p38 MAPK/Snail signaling pathway was involved in the occurrence of EMT in A549 cells treated by silica. EMT was inhibited by BMP-7. The data showed BMP-7 inhibited EMT induced by silica associated with inhibition of p38 MAPK/Snail pathway.

Keywords: Bone morphogenic protein-7; Epithelial–mesenchymal transition; Silica; Snail; p38 MAPK.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Morphogenetic Protein 7 / genetics
  • Bone Morphogenetic Protein 7 / metabolism*
  • Cadherins / genetics
  • Cadherins / metabolism
  • Cell Line, Tumor
  • Epithelial-Mesenchymal Transition*
  • Humans
  • Male
  • Rats
  • Rats, Wistar
  • Silicosis / metabolism*
  • Snail Family Transcription Factors
  • Transcription Factors / metabolism
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / metabolism
  • Vimentin / genetics
  • Vimentin / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Bmp7 protein, rat
  • Bone Morphogenetic Protein 7
  • Cadherins
  • Snai2 protein, rat
  • Snail Family Transcription Factors
  • Transcription Factors
  • Transforming Growth Factor beta
  • Vimentin
  • p38 Mitogen-Activated Protein Kinases