Activation of mitogen-activated protein kinase and p70S6 kinase is not correlated with cerebellar granule cell survival.

FJ Gunn-Moore, AG Williams, NJ Toms, JM Tavaré

Research output: Contribution to journalArticlepeer-review

Abstract

We have investigated the role of mitogen-activated protein (MAP) kinase in the survival of cerebellar granule cells in primary culture. Brain-derived neurotrophic factor (BDNF) and insulin, but not epidermal growth factor (EGF), promoted the survival of P6 cerebellar granule neurons. BDNF promoted a sustained activation of MAP kinase, whereas that induced by EGF was only transient. Insulin promoted a small but transient activation of MAP kinase that was completely blocked by PD98059, an inhibitor of MAP kinase kinase activation. PD98059 had no effect on the insulin- or BDNF-induced survival of cerebellar granule cells. We also investigated the role of p70S6 kinase in survival. The activation of p70S6 kinase by EGF was transient, whereas BDNF and insulin promoted a sustained activation of p70S6 kinase. Rapamycin, which blocked p70S6 kinase activation, had no effect on the BDNF- or insulin-induced survival of cerebellar granule cells. We conclude that sustained activation of MAP kinase is not correlated with the survival response of cerebellar granule cells; indeed insulin-mediated survival is independent of MAP kinase. Survival of cerebellar granule cells is also independent of the activation of p70S6 kinase.
Original languageEnglish
Pages (from-to)365-369
Number of pages0
JournalBiochem J
Volume0
Issue number0
DOIs
Publication statusPublished - 1 Jun 1997

Keywords

  • Amino Acid Sequence
  • Animals
  • Apoptosis
  • Brain-Derived Neurotrophic Factor
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Cell Survival
  • Cells
  • Cultured
  • Cerebellum
  • Culture Media
  • Serum-Free
  • Enzyme Activation
  • Enzyme Inhibitors
  • Epidermal Growth Factor
  • Flavonoids
  • Insulin
  • Molecular Sequence Data
  • Nerve Tissue Proteins
  • Neurons
  • Polyenes
  • Protein Serine-Threonine Kinases
  • Protein-Tyrosine Kinases
  • Rats
  • Ribosomal Protein S6 Kinases
  • Sirolimus

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