Phosphofructokinase-1 Negatively Regulates Neurogenesis from Neural Stem Cells

Neurosci Bull. 2016 Jun;32(3):205-16. doi: 10.1007/s12264-016-0032-y. Epub 2016 May 4.

Abstract

Phosphofructokinase-1 (PFK-1), a major regulatory glycolytic enzyme, has been implicated in the functions of astrocytes and neurons. Here, we report that PFK-1 negatively regulates neurogenesis from neural stem cells (NSCs) by targeting pro-neural transcriptional factors. Using in vitro assays, we found that PFK-1 knockdown enhanced, and PFK-1 overexpression inhibited the neuronal differentiation of NSCs, which was consistent with the findings from NSCs subjected to 5 h of hypoxia. Meanwhile, the neurogenesis induced by PFK-1 knockdown was attributed to the increased proliferation of neural progenitors and the commitment of NSCs to the neuronal lineage. Similarly, in vivo knockdown of PFK-1 also increased neurogenesis in the dentate gyrus of the hippocampus. Finally, we demonstrated that the neurogenesis mediated by PFK-1 was likely achieved by targeting mammalian achaete-scute homologue-1 (Mash 1), neuronal differentiation factor (NeuroD), and sex-determining region Y (SRY)-related HMG box 2 (Sox2). All together, our results reveal PFK-1 as an important regulator of neurogenesis.

Keywords: Hypoxia; Neural stem cell; Neurogenesis; Neuronal differentiation; Phosphofructokinase-1; Proliferation.

MeSH terms

  • Animals
  • Cell Differentiation / genetics*
  • Cell Hypoxia / physiology
  • Cells, Cultured
  • Cerebral Cortex / cytology
  • Embryo, Mammalian
  • Gene Expression Regulation / genetics
  • Gene Knockdown Techniques
  • Hippocampus / cytology
  • Hippocampus / metabolism
  • In Vitro Techniques
  • Mice
  • Mice, Inbred C57BL
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neural Stem Cells / cytology*
  • Neurogenesis / genetics*
  • Phosphofructokinase-1 / genetics*
  • Phosphofructokinase-1 / metabolism*
  • SOXB1 Transcription Factors / genetics
  • SOXB1 Transcription Factors / metabolism
  • Sex-Determining Region Y Protein / genetics
  • Sex-Determining Region Y Protein / metabolism
  • Time Factors

Substances

  • Nerve Tissue Proteins
  • SOXB1 Transcription Factors
  • Sex-Determining Region Y Protein
  • Sox2 protein, mouse
  • Phosphofructokinase-1