h-sgk serine-threonine protein kinase as transcriptional target of p38/MAP kinase pathway in HepG2 human hepatoma cells

Cell Physiol Biochem. 2000;10(4):203-8. doi: 10.1159/000016351.

Abstract

The human serum and glucocorticoid dependent serine/threonine kinase h-sgk has previously been discovered as cell volume regulated gene. The present study has been performed to elucidate the involvement of p38-kinase in the transcriptional control of h-sgk by osmotic cell shrinkage. The p38-kinase has previously been cloned as the mammalian homologue of HOG1 kinase, which constitutes a part of the osmosensor in the yeast Saccharomyces cerevisiae. Phosphorylated (active) p38-kinase has been estimated with Western blotting, transcription of hsgk using Northern blotting. Both, increase of extracellular NaCl concentration by 50 mmol/l and addition of 10 micromol/l anisomycin increase phosphorylation of the p38-kinase within 5 to 10 minutes. h-sgk transcription is upregulated by addition of 50 mmol/l NaCl and by anisomycin (10 micromol/l), effects completely inhibited by the specific p38-kinase inhibitor, SB 203580 (10 micromol/l). In conclusion, the stimulation of h-sgk transcription by osmotic cell shrinkage is mediated by p38-kinase.

MeSH terms

  • Anisomycin / pharmacology
  • Cell Size / drug effects
  • Enzyme Activation / drug effects
  • Gene Expression Regulation, Enzymologic* / drug effects
  • Humans
  • Imidazoles / pharmacology
  • Immediate-Early Proteins
  • MAP Kinase Signaling System* / drug effects
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinases / metabolism*
  • Nuclear Proteins*
  • Osmotic Pressure
  • Phosphorylation / drug effects
  • Protein Serine-Threonine Kinases / genetics*
  • Protein Serine-Threonine Kinases / metabolism
  • Pyridines / pharmacology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Sodium Chloride / pharmacology
  • Transcription, Genetic / drug effects
  • Transcription, Genetic / genetics*
  • Tumor Cells, Cultured
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Imidazoles
  • Immediate-Early Proteins
  • Nuclear Proteins
  • Pyridines
  • RNA, Messenger
  • Sodium Chloride
  • Anisomycin
  • Protein Serine-Threonine Kinases
  • serum-glucocorticoid regulated kinase
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • SB 203580