NGF mediates protection of mesenchymal stem cells-conditioned medium against 2,5-hexanedione-induced apoptosis of VSC4.1 cells via Akt/Bad pathway

Mol Cell Biochem. 2020 Jun;469(1-2):53-64. doi: 10.1007/s11010-020-03727-5. Epub 2020 Apr 11.

Abstract

It has been shown that the conditioned medium of bone mesenchymal stem cells (BMSC-CM) can inhibit apoptosis of neural cells exposed to 2,5-hexanedione (HD), but its protective mechanism remains unclear. To investigate the underlying mechanism, VSC4.1 cells were given HD and 5, 10 and 15% BMSC-CM (v/v) in the current experiment. Our data showed that BMSC-CM concentration-dependently attenuated HD-induced cell apoptosis. Moreover, BMSC-CM remarkably decreased the mitochondrial cytochrome c (Cyt C) release and the caspase-3 activity in HD-given VSC4.1 cells. Given a relatively high expression of NGF in BMSCs and BMSC-CM, we hypothesized that NGF might be an important mediator of the protection of BMSC-CM against apoptosis induced by HD. To verify our hypothesis, the VSC4.1 cells were administrated with NGF and anti-NGF antibody in addition to HD. As expected, NGF could perfectly mimic BMSC-CM's protective role and these beneficial effects were abolished by anti-NGF antibody intervention. To further explore its mechanism, inhibitors of TrkA and Akt were given to the VSC4.1 cells and NGF/Akt/Bad pathway turned out to be involved in anti-apoptotic role of BMSC-CM. Based on these findings, it was revealed that BMSC-CM beneficial role was mediated by NGF and relied on the Akt/Bad pathway.

Keywords: 2,5-Hexanedione (HD); Akt/bad pathway; Apoptosis; Conditioned medium of bone mesenchymal stem cells (BMSC-CM); Nerve growth factor (NGF); VSC4.1 cells.

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Caspase 3 / metabolism
  • Culture Media, Conditioned / pharmacology*
  • Cytochromes c / metabolism
  • Hexanones / toxicity*
  • Mesenchymal Stem Cells / metabolism*
  • Microscopy, Electron, Transmission
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Nerve Growth Factor / metabolism
  • Nerve Growth Factor / pharmacology*
  • Neurons / drug effects*
  • Neurons / metabolism
  • Neurons / ultrastructure
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Rats
  • Receptor, trkA / antagonists & inhibitors
  • Signal Transduction / drug effects
  • bcl-Associated Death Protein / metabolism*

Substances

  • Bad protein, rat
  • Culture Media, Conditioned
  • Hexanones
  • bcl-Associated Death Protein
  • Cytochromes c
  • Nerve Growth Factor
  • 2,5-hexanedione
  • Receptor, trkA
  • Proto-Oncogene Proteins c-akt
  • Caspase 3