Mechanism of TNF-α-induced migration and hepatocyte growth factor production in human mesenchymal stem cells

J Cell Biochem. 2010 Oct 1;111(2):469-75. doi: 10.1002/jcb.22729.

Abstract

Accumulating evidence suggests that mesenchymal stem cells (MSCs) may decrease destructive inflammation and reduce tissue loss. Tumor necrosis factor-α (TNF-α) plays a central role in induction of proinflammatory signaling and paradoxically activates intracellular anti-inflammatory survival pathways. In this study, we investigated whether TNF-α could induce a chemotactic effect on human MSCs and stimulate their production of anti-inflammatory factors in vitro, as well as determined mechanisms that mediated this effect. Migration assays demonstrated that TNF-α had a chemotactic effect on MSCs. TNF-α increased both hepatocyte growth factor (HGF) mRNA expression in MSCs and HGF secretion in conditioned medium. These effects were dependent on the p38 MAPK and PI3K/Akt, but not JNK and ERK signaling pathways. Furthermore, these effects were inhibited by a specific neutralizing antibody to TNF receptor II, but not TNF receptor I. We conclude that TNF-α can enhance human MSCs migration and stimulate their production of HGF. These effects are mediated via a specific TNF receptor and signaling pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Movement / drug effects
  • Cells, Cultured
  • Culture Media, Conditioned
  • Hepatocyte Growth Factor / biosynthesis*
  • Humans
  • Mesenchymal Stem Cells
  • RNA, Messenger / analysis
  • Receptors, Tumor Necrosis Factor
  • Signal Transduction
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Culture Media, Conditioned
  • RNA, Messenger
  • Receptors, Tumor Necrosis Factor
  • Tumor Necrosis Factor-alpha
  • Hepatocyte Growth Factor