Lin28b and Sox2 regulate anesthesia-induced neural degeneration in neural stem cell derived neurons

Eur J Pharmacol. 2018 Feb 5:820:167-172. doi: 10.1016/j.ejphar.2017.12.031. Epub 2017 Dec 12.

Abstract

Ketamine, a commonly used anesthetic compound, may cause neurotoxicity in immature or developing brains. In this study, we indented to understand the molecular expression and functional role of Lin-28 Homolog B (lin28b) in regulating ketamine-induced neurotoxicity in neural stem cells (NSCs)-differentiated neurons. NSCs from embryonic rat brains were cultured in vitro, and induced toward neuronal differentiation. NSCs-differentiated neurons were treated with various concentrations of ketamine for 24h to evaluate the concentration-dependent effect of ketamine on endogenous lin28b mRNA level. QRT-PCR showed that lin28b was downregulated by ketamine in NSCs-differentiated neurons, in concentration-dependent manner. Neurons were then transfected with adenovirus to ectopically upregulate lin28b. We found that ketamine-induced apoptosis and neurite retraction in NSCs-differentiated neurons were significantly reduced by adenovirus-mediated lin28b upregulation. Expression of sex determining region Y box 2 (Sox2) mRNA was examined in ketamine-injured and lin28b-upregulated NSCs-differentiated neurons. It was found Sox2 was downregulated by ketamine, and overexpressed by lin28b upregulation. Finally, Sox2 was downregulated by siRNA in NSCs-differentiated neurons. And we discovered that Lin28b-upregulation-associated neural protection was severely hampered by Sox2 downregulation in ketamine-injured neurons. Thus, Lin28b and Sox2 are important molecular components in ketamine-induced neurotoxicity.

Keywords: Ketamine; Lin28b; Neural differentiation; Neural stem cell; Neurotoxicity; Sox2.

MeSH terms

  • Anesthetics / toxicity*
  • Animals
  • Cell Differentiation / drug effects
  • Female
  • Ketamine / toxicity
  • Nerve Degeneration / chemically induced*
  • Nerve Degeneration / metabolism
  • Nerve Degeneration / pathology
  • Neural Stem Cells / cytology*
  • Neurons / cytology
  • Neurons / drug effects*
  • Neurons / metabolism*
  • Pregnancy
  • RNA-Binding Proteins / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • SOXB1 Transcription Factors / metabolism*
  • Up-Regulation / drug effects

Substances

  • Anesthetics
  • Lin28A protein, rat
  • RNA-Binding Proteins
  • SOXB1 Transcription Factors
  • Sox2 protein, rat
  • Ketamine