Intracellular signal transduction of interferon on the suppression of haematopoietic progenitor cell growth

Br J Haematol. 2003 Nov;123(3):528-35. doi: 10.1046/j.1365-2141.2003.04650.x.

Abstract

Interferon (IFN)-alpha and IFN-gamma suppress the growth of haematopoietic progenitor cells. IFN-alpha activates Janus kinase-1 (Jak1) and Tyrosine kinase-2 (Tyk2), followed by the phosphorylation of the signal transducers and activators of transcription, Stat1 and Stat2. IFN-gamma activates Jak1 and Jak2, followed by the activation of Stat1. Activated Stats bind the promoter regions of IFN-inducible genes. We evaluated the role of Tyk2 and Stat1 in the IFN-mediated inhibition of haematopoietic progenitor cell growth. While IFN-alpha (1000 U/ml) suppressed the number of granulocyte-macrophage colony-forming units (CFU-GM) or erythroid burst-forming units (BFU-E) from wild-type mouse bone marrow cells, this suppression was partially inhibited by a deficiency in Tyk2 and completely inhibited by a deficiency in Stat1. High levels of IFN-alpha (10,000 U/ml) suppressed the CFU-GM or BFU-E obtained from Stat1-deficient mice, but did not suppress this growth in cells from Tyk2-deficient mice. Stat1 was phosphorylated by IFN-alpha in Tyk2-deficient cells, although the level of phosphorylation was weaker than that observed in wild type mice. Thus, the inhibitory signal on haematopoietic progenitor cells mediated by IFN-alpha may be transduced by two signalling pathways, one regulated by Tyk2 and the other dependent on Stat1. IFN-gamma also suppressed the number of CFU-GM or BFU-E, and this pathway was mediated by IFN-gamma in a Stat1-dependent manner, independently of Tyk2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division / physiology
  • Colony-Forming Units Assay
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Depression, Chemical
  • Hematopoietic Stem Cells / physiology*
  • Interferon-alpha / pharmacology
  • Interferon-gamma / pharmacology
  • Interferons / pharmacology*
  • Intracellular Fluid / immunology*
  • Mice
  • Mice, Knockout
  • Phosphorylation
  • Protein-Tyrosine Kinases*
  • Proteins / genetics
  • Proteins / metabolism*
  • STAT1 Transcription Factor
  • Signal Transduction / physiology*
  • TYK2 Kinase
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*

Substances

  • DNA-Binding Proteins
  • Interferon-alpha
  • Proteins
  • STAT1 Transcription Factor
  • Stat1 protein, mouse
  • Trans-Activators
  • Interferon-gamma
  • Interferons
  • Protein-Tyrosine Kinases
  • TYK2 Kinase
  • Tyk2 protein, mouse