L-Cysteine promotes the proliferation and differentiation of neural stem cells via the CBS/H₂S pathway

Neuroscience. 2013 May 1:237:106-17. doi: 10.1016/j.neuroscience.2012.12.057. Epub 2013 Jan 30.

Abstract

Growing evidence has suggested that hydrogen sulfide (H₂S) acts as a novel neuro-modulator and neuroprotective agent; however, it remains to be investigated whether H2S has a direct effect on neural stem cells (NSCs). We report here that NSCs expressed cystathionine β synthase (CBS) and addition of exogenous H2S donor, L-cysteine, stimulated proliferation and increased the differentiation potential of NSCs to neurons and astroglia. Moreover, pre-treatment with aminooxyacetic acid, the inhibitor of CBS or knockdown of CBS in using siRNA, significantly attenuated the effects of L-cysteine on elevated H₂S levels and the cell proliferation; it also effectively suppressed L-cysteine-induced neurogenesis and astrocytogenesis. Further analysis revealed that L-cysteine-induced proliferation was associated with phosphorylation of extracellular signal-regulated kinases 1/2 and differentiation with altered expression of differentiation-related genes. Taken together, the present data suggest that L-cysteine can enhance proliferation and differentiation of NSCs via the CBS/H2S pathway, which may serve as a useful inference for elucidating its role in regulating the fate of NSCs in physiological and pathological settings.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Bromodeoxyuridine / metabolism
  • Cell Differentiation / drug effects*
  • Cell Proliferation / drug effects*
  • Cell Survival / drug effects
  • Cystathionine beta-Synthase / metabolism*
  • Cysteine / pharmacology*
  • Dose-Response Relationship, Drug
  • Embryo, Mammalian
  • Flow Cytometry
  • Gene Expression Regulation / drug effects
  • Hydrogen Sulfide / metabolism*
  • Mice
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neural Stem Cells / drug effects*
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / pharmacology
  • Signal Transduction / drug effects
  • Tacrolimus / analogs & derivatives
  • Tacrolimus / pharmacology
  • Telencephalon / cytology
  • Time Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • 32-ascomycinyloxyacetic acid
  • Nerve Tissue Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • Transcription Factors
  • Cystathionine beta-Synthase
  • Bromodeoxyuridine
  • Cysteine
  • Tacrolimus
  • Hydrogen Sulfide