Interferon-alpha inhibits cell cycle progression by Ba/F3 cells through the antagonisation of interleukin-3 effects on key regulators of G(1)/S transition

Cell Signal. 2002 Sep;14(9):751-9. doi: 10.1016/s0898-6568(02)00023-2.

Abstract

The molecular mechanisms of interferon-alpha (IFN-alpha)-mediated cell growth inhibition are incompletely understood. Here, we have analysed how IFN-alpha interferes with the interleukin-3 (IL-3)-stimulated cell cycle progression by Ba/F3 cells. The antiproliferative cytokine caused a delay in cell cycle progression, which correlated with a diminished activation of the cyclin-dependent kinases 2 and 4 in IL-3-stimulated cells. While IFN-alpha did not affect the expression of p27(Kip1) and p21(Waf1), it efficiently inhibited the IL-3-induced expression of D-type cyclin and cyclin E proteins. No IL-3-antagonistic effects of the IFN, however, were observed at the mRNA level of cyclin expression. Furthermore, IFN-alpha suppressed the IL-3-induced release of E2F transcription factors from the retinoblastoma protein (pRb) and enhanced pRb-mediated transcriptional repression. The growth factor-antagonistic action of IFN-alpha correlated with a strong stimulation of protein kinase R expression, suggesting that inhibition of protein synthesis plays a pivotal role in IFN-alpha-mediated inhibition of cell cycle progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle Proteins / metabolism*
  • Cell Cycle* / drug effects
  • Cell Line
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinases / metabolism
  • Cyclins / biosynthesis
  • Cyclins / genetics
  • Cyclins / metabolism
  • DNA-Binding Proteins / metabolism
  • E2F Transcription Factors
  • G1 Phase / drug effects
  • Interferon-alpha / pharmacology*
  • Interleukin-3 / antagonists & inhibitors*
  • Mice
  • RNA, Messenger / biosynthesis
  • Repressor Proteins / antagonists & inhibitors
  • Retinoblastoma Protein / antagonists & inhibitors
  • S Phase
  • Transcription Factors / metabolism
  • Tumor Suppressor Proteins / metabolism
  • eIF-2 Kinase / metabolism

Substances

  • Cdkn1a protein, mouse
  • Cdkn1b protein, mouse
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • DNA-Binding Proteins
  • E2F Transcription Factors
  • Interferon-alpha
  • Interleukin-3
  • RNA, Messenger
  • Repressor Proteins
  • Retinoblastoma Protein
  • Transcription Factors
  • Tumor Suppressor Proteins
  • Cyclin-Dependent Kinase Inhibitor p27
  • eIF-2 Kinase
  • Cyclin-Dependent Kinases