Substance P induced biosynthesis of the zinc finger transcription factor Egr-1 in human glioma cells requires activation of the epidermal growth factor receptor and of extracellular signal-regulated protein kinase

Neurosci Lett. 2002 Oct 31;332(2):111-4. doi: 10.1016/s0304-3940(02)00939-4.

Abstract

Substance P is a member of the tachykinin family of neuropeptides that plays an important role in pain transmission, neurogenic inflammatory diseases and the adaptive response to stress. Substance P exerts its biological activities via binding to a G-protein coupled receptor of the neurokinin (NK) receptor family. Here, we show by Western blot experiments that substance P induced a transient synthesis of the zinc finger transcriptional regulator Egr-1 in human glioma cells. Substance P-induced stimulation of Egr-1 biosynthesis was completely inhibited by the mitogen-activated protein kinase kinase inhibitor PD98059 and by AG1487, an epidermal growth factor (EGF) receptor-specific tyrosine kinase inhibitor. These results indicate that transactivation of the EGF receptor as well as stimulation of the mitogen activated/extracellular signal-regulated protein kinase (ERK) are essential for substance P/NK-1 receptor-induced activation of Egr-1 biosynthesis. Moreover, we show that the signaling cascade initiated by substance P or EGF are indistinguishable, including the activation of the EGF receptor, the activation of ERK, and the final stimulation of Egr-1 biosynthesis. The synthesis of Egr-1 in glioma cells as a result of substance P stimulation suggests that substance P exerts long-term effects in glioma cells via Egr-1-mediated gene transcription.

MeSH terms

  • Culture Media, Serum-Free
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / genetics*
  • Early Growth Response Protein 1
  • Enzyme Inhibitors / pharmacology
  • ErbB Receptors / drug effects*
  • ErbB Receptors / metabolism
  • Flavonoids / pharmacology
  • GTP-Binding Proteins / metabolism
  • Glioma / genetics*
  • Glioma / metabolism
  • Humans
  • Immediate-Early Proteins*
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinases / metabolism
  • Mitogen-Activated Protein Kinases / physiology*
  • Receptors, Neurokinin-1 / biosynthesis
  • Receptors, Neurokinin-1 / genetics
  • Substance P / pharmacology*
  • Transcription Factors / biosynthesis
  • Transcription Factors / genetics*
  • Tumor Cells, Cultured
  • Zinc Fingers / genetics*

Substances

  • Culture Media, Serum-Free
  • DNA-Binding Proteins
  • EGR1 protein, human
  • Early Growth Response Protein 1
  • Enzyme Inhibitors
  • Flavonoids
  • Immediate-Early Proteins
  • Receptors, Neurokinin-1
  • Transcription Factors
  • Substance P
  • ErbB Receptors
  • Mitogen-Activated Protein Kinases
  • GTP-Binding Proteins
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one