Cytokine-induced transcription of protein-tyrosine-phosphatases in human astrocytoma cells

Brain Res Mol Brain Res. 1998 Nov 12;62(1):56-64. doi: 10.1016/s0169-328x(98)00237-x.

Abstract

Interleukin-1 (IL-1) and Tumor Necrosis Factor-a (TNFalpha) are potent mediators of inflammatory reactions in the brain. Although much is known about the effects of IL-1 on expression of secretory proteins, few studies have addressed the question of a selective, IL-1-dependent expression of genes involved in neuromodulatory effects of inflammation. Protein-tyrosine-phosphatases (PTP's) have been shown to regulate signal transduction and adhesion processes in the developing nervous system. They are candidates for inflammation-induced neuromodulation. Therefore, we investigated if IL-1 regulates expression of PTP's. We applied a DNA-fingerprinting method based on the PCR-amplification of conserved domains of gene families and observed IL-1-dependent induction of two PTP's, cytoplasmic PTPvarepsilon and receptor-PTPgamma, RPTPgamma, in human U373-MG astrocytoma cells. Using Northern blot analysis, we confirmed this result and also show that in addition to IL-1, TNFalpha but not IL-6 induces the transcription of cytoplasmic PTPvarepsilon and RPTPgamma in human astrocytoma cells. Given the important role for PTP's in neuromodulatory aspects such as axonal guidance and neurite outgrowth, cytokine-induced induction of PTP's may play an important pathenogenic role in the development of chronic inflammatory diseases in the brain.

MeSH terms

  • Astrocytoma / enzymology*
  • Astrocytoma / genetics
  • Base Sequence
  • Blotting, Northern
  • Cytokines / pharmacology*
  • DNA, Complementary / analysis
  • Electrophoresis, Polyacrylamide Gel
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Interleukin-1 / pharmacology
  • Interleukin-6 / pharmacology
  • Molecular Sequence Data
  • Nerve Tissue Proteins / chemistry
  • Nerve Tissue Proteins / drug effects
  • Nerve Tissue Proteins / genetics
  • Polymerase Chain Reaction
  • Protein Tyrosine Phosphatases / biosynthesis*
  • Protein Tyrosine Phosphatases / chemistry
  • Protein Tyrosine Phosphatases / drug effects*
  • Protein Tyrosine Phosphatases / genetics
  • RNA, Messenger / analysis
  • RNA, Messenger / drug effects
  • Receptor-Like Protein Tyrosine Phosphatases, Class 4
  • Receptor-Like Protein Tyrosine Phosphatases, Class 5
  • Receptors, Cell Surface
  • Sequence Analysis, DNA
  • Transcription, Genetic / drug effects*
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Cytokines
  • DNA, Complementary
  • Interleukin-1
  • Interleukin-6
  • Nerve Tissue Proteins
  • RNA, Messenger
  • Receptors, Cell Surface
  • Tumor Necrosis Factor-alpha
  • PTPRE protein, human
  • PTPRG protein, human
  • Protein Tyrosine Phosphatases
  • Receptor-Like Protein Tyrosine Phosphatases, Class 4
  • Receptor-Like Protein Tyrosine Phosphatases, Class 5