Activation of JNKs is essential for BMP9-induced osteogenic differentiation of mesenchymal stem cells

BMB Rep. 2013 Aug;46(8):422-7. doi: 10.5483/bmbrep.2013.46.8.266.

Abstract

Although BMP9 is highly capable of promoting osteogenic differentiation of mesenchymal stem cell (MSCs), the molecular mechanism involved remains to be fully elucidated. Here, we explore the possible involvement and detail role of JNKs (c-Jun N-terminal kinases) in BMP9-induced osteogenic differentiation of MSCs. It was found that BMP9 stimulated the activation of JNKs in MSCs. BMP9-induced osteogenic differentiation of MSCs was dramatically inhibited by JNKs inhibitor SP600125. Moreover, BMP9-activated Smads signaling was decreased by SP600125 treatment in MSCs. The effects of inhibitor are reproduced with adenoviruses expressing siRNA targeted JNKs. Taken together, our results revealed that JNKs was activated in BMP9-induced osteogenic differentiation of MSCs. What is most noteworthy, however, is that inhibition of JNKs activity resulted in reduction of BMP9-induced osteogenic differentiation of MSCs, implying that activation of JNKs is essential for BMP9 osteoinductive activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anthracenes / pharmacology
  • Cell Differentiation / drug effects*
  • Cells, Cultured
  • Growth Differentiation Factors / pharmacology*
  • HCT116 Cells
  • Humans
  • JNK Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • JNK Mitogen-Activated Protein Kinases / genetics
  • JNK Mitogen-Activated Protein Kinases / metabolism*
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • Osteogenesis / drug effects*
  • Phosphorylation / drug effects
  • RNA Interference
  • RNA, Small Interfering
  • Signal Transduction / drug effects
  • Smad Proteins / metabolism

Substances

  • Anthracenes
  • Growth Differentiation Factors
  • RNA, Small Interfering
  • Smad Proteins
  • pyrazolanthrone
  • JNK Mitogen-Activated Protein Kinases