Ras is not required for the interleukin 3-induced proliferation of a mouse pro-B cell line, BaF3

J Biol Chem. 1995 Nov 17;270(46):27880-6. doi: 10.1074/jbc.270.46.27880.

Abstract

It has been demonstrated that Ras is involved in interleukin 3 (IL-3)-stimulated signal transduction in various hematopoietic cultured cells (Satoh, T., Nakafuku, M., Miyajima, A., and Kaziro, Y. (1991) Proc. Natl. Acad. Sci. U.S.A. 88, 3314-3318; Duronio, V., Welham, M. J., Abraham, S., Dryden, P., and Schrader, J. W. (1992) Proc. Natl. Acad. Sci. U.S.A. 89, 1587-1591). However, it has not been fully understood which of IL-3-promoted cellular responses, i.e. proliferation, survival, and differentiation, requires Ras function. We employed a system of inducible expression of the dominant-negative (S17N) or dominant-active (G12V) mutant of Ras in BaF3 mouse pro-B cell line to analyze the role of Ras in IL-3-stimulated signal transduction. Induction of the dominant-negative Ras(S17N) effectively inhibited the IL-3-induced activation of c-Raf-1 and mitogen-activated protein kinase (MAPK). Furthermore, the activation of fos gene promoter following IL-3 stimulation was almost completely abolished when Ras(S17N) was induced. Under these conditions, Ras(S17N) exhibited no inhibitory effect on IL-3-dependent proliferation assessed by the increase of cell numbers and a mitochondrial enzyme activity. The results indicate that Ras-dependent pathways, including the Raf/MAPK/Fos pathway, are dispensable for IL-3-induced growth stimulation. When BaF3 cells were treated with a tyrosine kinase inhibitor, herbimycin A, IL-3-dependent proliferation of the cells was impaired, suggesting that tyrosine kinase-mediated pathways are critical for growth promotion. On the other hand, apoptotic cell death caused by deprivation of IL-3 was prevented by the induction of the activated mutant Ras(G12V), although the rate of cell number increase was markedly reduced. Thus, it is likely that Ras-independent pathways play important roles to facilitate the proliferation although they may not be essential for IL-3-stimulated antiapoptotic signal transduction.

MeSH terms

  • Animals
  • B-Lymphocytes
  • Benzoquinones
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Cell Division / drug effects*
  • Cell Line
  • Cloning, Molecular
  • Enzyme Inhibitors / pharmacology
  • Genes, fos
  • Genes, ras*
  • Guanine Nucleotides / metabolism
  • Humans
  • Immune Sera
  • Interleukin-3 / pharmacology*
  • Lactams, Macrocyclic
  • MAP Kinase Kinase Kinase 1*
  • Mice
  • Promoter Regions, Genetic
  • Protein Serine-Threonine Kinases / metabolism*
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-raf
  • Proto-Oncogene Proteins p21(ras) / biosynthesis
  • Proto-Oncogene Proteins p21(ras) / immunology
  • Proto-Oncogene Proteins p21(ras) / physiology*
  • Quinones / pharmacology
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / metabolism
  • Rifabutin / analogs & derivatives
  • Signal Transduction*
  • Transfection
  • ras Proteins / metabolism*

Substances

  • Benzoquinones
  • Enzyme Inhibitors
  • Guanine Nucleotides
  • Immune Sera
  • Interleukin-3
  • Lactams, Macrocyclic
  • Proto-Oncogene Proteins
  • Quinones
  • Recombinant Fusion Proteins
  • Rifabutin
  • herbimycin
  • Protein-Tyrosine Kinases
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-raf
  • Calcium-Calmodulin-Dependent Protein Kinases
  • MAP Kinase Kinase Kinase 1
  • MAP3K1 protein, human
  • Map3k1 protein, mouse
  • HRAS protein, human
  • Proto-Oncogene Proteins p21(ras)
  • ras Proteins