TGF-β Induces Up-Regulation of Chondroitin Sulfate Synthase 1 (CHSY1) in Nucleus Pulposus Cells Through MAPK Signaling

Cell Physiol Biochem. 2015;37(2):793-804. doi: 10.1159/000430396. Epub 2015 Sep 11.

Abstract

Background/aims: Chondroitin sulfate synthase 1 (CHSY1) is a glycosyltransferases involved in the biosynthesis of chondroitin and dermatan sulfate glycosaminoglycan (GAG). TGF-β can stimulate sulfated GAG production in nucleus pulposus cells; however, the underlying mechanisms are poorly understood.

Methods: CHSY1 expression was examined in rat nucleus pulposus treated with TGF-β using real-time PCR and Western blot analysis. Lentiviral knockdown was performed to determine the downstream effectors of TGF-β and to measure the effect of c-Jun and Sp1 on TGF-β mediated CHSY1 promoter activity and CHSY1 expression.

Results: TGF-β increased CHSY1 expression and promoter activity in the nucleus pulposus partially through activation of canonical Smad signaling pathway. Knockdown of c-Jun and Sp1 decreased CHSY1 promoter activity, CHSY1 expression and sGAG accumulation induced by TGF-β. Furthermore, we found that TGF-β-induced expression of CHSY1 was mediated through the activation of MAPK signaling. Moreover, we showed that silencing CHSY1 decreased sGAG accumulation in nucleus pulposus cells induced by TGF-β.

Conclusion: Our results suggest that TGF-β induced CHSY1 expression in the nucleus pulposus through the activation of MAPK signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Glucuronosyltransferase / metabolism*
  • Intervertebral Disc / enzymology
  • Intervertebral Disc / metabolism*
  • MAP Kinase Signaling System
  • Multifunctional Enzymes / metabolism*
  • N-Acetylgalactosaminyltransferases / genetics*
  • N-Acetylgalactosaminyltransferases / metabolism*
  • Promoter Regions, Genetic / drug effects
  • Rats
  • Sp1 Transcription Factor / genetics
  • Sp1 Transcription Factor / metabolism
  • Transforming Growth Factor beta3 / metabolism*
  • Up-Regulation

Substances

  • Multifunctional Enzymes
  • Sp1 Transcription Factor
  • Transforming Growth Factor beta3
  • CHSY1 protein, rat
  • N-Acetylgalactosaminyltransferases
  • Glucuronosyltransferase