Oncostatin M activates stat DNA binding and transcriptional activity in primary human fetal astrocytes: low- and high-passage cells have distinct patterns of stat activation

Cytokine. 2000 Nov;12(11):1647-55. doi: 10.1006/cyto.2000.0774.

Abstract

In this study we explored the activation of the JAK/Stat pathway by gp 130 family cytokines in primary human astrocytes. We report that of four gp 130 cytokines tested, only oncostatin M (OnM) resulted in the activation of Stat molecules. To test that the induced molecules were transcriptionally active, transcription from a Stat-responsive reporter plasmid (from the acute-phase gene alpha-2 macroglobulin) transiently transfected into astrocytes was assessed after activation by OnM and was blocked by cotransfection with dominant-negative Stat3 encoding plasmids strongly suggesting that the activation was Stat-mediated. While DNA binding complexes comprised of both Stat1 and Stat3 were induced in low-passage cells, only those containing Stat3 were formed by extracts from high-passage cells. Stat1 protein was detected in the cytoplasm of high-passage cells indicating that the inability to form SIF-B and -C complexes was due to a lack of activation of Stat1 rather than a lack of expression. These results indicate a fundamental difference between low- and high-passage astrocytes in response to cytokine treatment that might result in distinct patterns of gene expression through altered ratios of activated Stat3 and Stat1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Astrocytes / metabolism*
  • Cell Culture Techniques
  • Cell Line
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Chloramphenicol O-Acetyltransferase / metabolism
  • Cytoplasm / metabolism
  • DNA / metabolism*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Embryo, Mammalian / metabolism*
  • Enzyme Activation
  • Genes, Dominant
  • Genes, Reporter
  • Growth Inhibitors / pharmacology
  • Humans
  • Immunoblotting
  • Oncostatin M
  • Peptides / pharmacology*
  • Peptides / physiology*
  • Plasmids / metabolism
  • Protein Binding
  • Proto-Oncogene Proteins c-sis / metabolism
  • STAT1 Transcription Factor
  • STAT3 Transcription Factor
  • Time Factors
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Transcription, Genetic*
  • Transcriptional Activation
  • Transfection
  • alpha-Macroglobulins / metabolism
  • beta-Galactosidase / metabolism

Substances

  • DNA-Binding Proteins
  • Growth Inhibitors
  • OSM protein, human
  • Peptides
  • Proto-Oncogene Proteins c-sis
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Trans-Activators
  • alpha-Macroglobulins
  • Oncostatin M
  • DNA
  • Chloramphenicol O-Acetyltransferase
  • beta-Galactosidase