Interferon-alpha inhibits proliferation in human T lymphocytes by abrogation of interleukin 2-induced changes in cell cycle-regulatory proteins

Cell Growth Differ. 1999 Aug;10(8):575-82.

Abstract

IFN-alpha exerts prominent regulatory functions on the immune system. One such effect is the inhibition of proliferation of in vitro stimulated T lymphocytes. The exact physiological function of this activity is not known, but it has been implicated in the antiviral effects of IFN, its antitumor action in T-cell malignancies, and the regulation of the in vivo T-cell response. Here, we have investigated the mechanism underlying the IFN-alpha-mediated growth inhibition of normal human PHA- and IL-2-stimulated T lymphocytes by an analysis of how IFN-alpha treatment influences known molecular events that normally accompany the transition from quiescence to proliferation in these cells. IFN-alpha treatment was found to profoundly block S-phase entry of stimulated T lymphocytes. This correlated with a strong inhibition of IL-2-induced changes in G1-regulatory proteins, including the prevented up-regulation of G1 cyclins and cyclin-dependent kinases as well as an abrogation of mitogen-induced reduction of p27Kip1 levels. This latter effect was due to a maintained stability of the p27Kip1 protein in the IFN-alpha-treated cells. In line with these findings, phosphorylation of the pocket proteins was abrogated in IFN-alpha-treated cells. Furthermore, our data indicate that IFN-alpha has selective effects on the pathways that emerge from the IL-2 receptor because IFN-alpha treatment does not block IL-2-induced up-regulation of c-myc or Cdc25A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Northern
  • Cell Cycle / drug effects
  • Cell Cycle Proteins / metabolism*
  • Cells, Cultured
  • Cyclin G
  • Cyclin G1
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinases / metabolism
  • Cyclins / metabolism
  • Humans
  • Interferon-alpha / pharmacology*
  • Interleukin-2 / pharmacology*
  • Lymphocyte Activation / drug effects
  • Microtubule-Associated Proteins / metabolism
  • Phytohemagglutinins / pharmacology
  • Protein Processing, Post-Translational / drug effects
  • Proto-Oncogene Proteins c-myc / biosynthesis
  • RNA, Messenger / metabolism
  • T-Lymphocytes / cytology
  • T-Lymphocytes / drug effects*
  • T-Lymphocytes / metabolism
  • Time Factors
  • Tumor Suppressor Proteins*
  • Up-Regulation / drug effects
  • cdc25 Phosphatases / biosynthesis

Substances

  • CCNG1 protein, human
  • Cell Cycle Proteins
  • Cyclin G
  • Cyclin G1
  • Cyclins
  • Interferon-alpha
  • Interleukin-2
  • Microtubule-Associated Proteins
  • Phytohemagglutinins
  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • Tumor Suppressor Proteins
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinases
  • CDC25A protein, human
  • cdc25 Phosphatases