Methylmercury induces caspase-dependent apoptosis and autophagy in human neural stem cells

J Toxicol Sci. 2013;38(6):823-31. doi: 10.2131/jts.38.823.

Abstract

Methylmercury (MeHg) is a well-known human neurotoxic agent whose exposure sources are mainly environmental and aquatic-derived food. MeHg is reported to induce central nervous system disability. However, the exact mechanism of MeHg-induced neurotoxicity is still unknown. In this study, to investigate which cell death signaling pathway is related with MeHg-induced cytotoxicity, the effects of MeHg on apoptosis and autophagy were evaluated in HB1.F3 human neural stem cells (NSCs). Human NSCs were treated with 1 μM of MeHg for 48 hr and the effect of MeHg on cell signaling pathway was elucidated. MeHg inhibited Akt1/mTOR signaling that led to induction of caspase-dependent apoptosis and autophagy in the NSCs. Furthermore, retinoic acid (RA)-induced neuronal differentiation was inhibited by MeHg. Taken together, these results suggest that MeHg inhibits the differentiation of human NSCs by induction of caspase-dependent apoptosis and autophagy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Apoptosis / genetics*
  • Autophagy / drug effects*
  • Autophagy / genetics*
  • Caspases / physiology*
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Humans
  • Methylmercury Compounds / toxicity*
  • Neural Stem Cells / cytology
  • Neural Stem Cells / drug effects*
  • Neural Stem Cells / pathology*
  • Signal Transduction / drug effects*
  • Signal Transduction / genetics*
  • Tretinoin / antagonists & inhibitors
  • Tretinoin / pharmacology

Substances

  • Methylmercury Compounds
  • Tretinoin
  • Caspases
  • methylmercuric chloride