Deregulated c-myc expression overrides IFN gamma-induced macrophage growth arrest

Oncogene. 1995 May 18;10(10):1969-76.

Abstract

Induction of c-myc gene expression is an essential response to growth promoting agents, including colony-stimulating factor 1 (CSF-1). Down regulation of c-myc expression occurs in response to a variety of negative growth regulators in many cell types. However, for many of these systems the causal link between c-myc down regulation and growth arrest remains to be established. Here we show for CSF-1-dependent BAC1.2F5 mouse macrophages that interferon-gamma (IFN gamma) results in a midlate G1 phase decrease of CSF-1-dependent c-myc mRNA and subsequent cell cycle arrest. Introduction of a deregulated c-myc gene into these cells, which prevents the IFN gamma-mediated decrease in c-myc expression, overrides the cell cycle arrest and restores CSF-1-dependent growth in the presence of the cytokine. This result contrasts with the macrophage growth arrest induced by cAMP elevation, which also suppresses c-myc expression, but is not overcome by a deregulated c-myc gene. These results show that inhibition of c-myc expression is an essential component in IFN gamma-mediated cell cycle arrest and demonstrates that distinct mechanisms contribute to IFN gamma- and cAMP-mediated growth arrest in macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division / drug effects
  • Cell Division / genetics
  • Cell Line
  • Cyclic AMP / metabolism
  • DNA / biosynthesis
  • Down-Regulation
  • Gene Expression Regulation
  • Genes, myc / drug effects
  • Genes, myc / physiology*
  • Interferon-gamma / pharmacology
  • Interferon-gamma / physiology*
  • Macrophage Colony-Stimulating Factor / physiology
  • Macrophages / cytology*
  • Mice
  • Proto-Oncogene Proteins c-myc / metabolism*
  • RNA, Messenger / metabolism

Substances

  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • Macrophage Colony-Stimulating Factor
  • Interferon-gamma
  • DNA
  • Cyclic AMP