Raf-1 is a necessary component of the mitogenic response of the human megakaryoblastic leukemia cell line MO7 to human stem cell factor, granulocyte-macrophage colony-stimulating factor, interleukin 3, and interleukin 9

Cell Growth Differ. 1994 Apr;5(4):367-72.

Abstract

We have examined the role of Raf-1 in the mitogenic response of the factor-deprived human megakaryoblastic leukemia cell line MO7 to recombinant human granulocyte-macrophage colony-stimulating factor, interleukin 3, interleukin 9, and stem cell factor by using c-raf antisense oligodeoxyribonucleotides. Uptake of oligodeoxyribonucleotides by MO7 cells was maximal at 5-10 h in culture, and oligomers remained stable in these cells for at least 24 h. Treatment of MO7 cells with the antisense oligomer resulted in intracellular oligomer/mRNA duplex formation followed by efficient translation blockade of c-raf-1. In contrast, sense and non-sense oligodeoxyribonucleotides failed to form intracellular duplexes and did not interfere with translation of c-raf-1, suggesting specific elimination of c-raf-1 by the antisense oligodeoxyribonucleotide. Furthermore, exposure of MO7 cells to c-raf-1 antisense prevented factor-induced nuclear translocation of Raf-1. Most importantly, proliferation of MO7 cells ([3H]thymidine incorporation) enabled by these growth factors was significantly reduced when the c-raf-1 antisense oligodeoxyribonucleotide was added to cultures, whereas the mitogenic response to these factors remained almost unaffected in the presence of sense and non-sense oligodeoxyribonucleotides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cell Division / drug effects
  • Codon / genetics
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Growth Substances / pharmacology*
  • Hematopoietic Cell Growth Factors / pharmacology
  • Humans
  • Interleukin-3 / pharmacology
  • Interleukin-9 / pharmacology
  • Leukemia, Megakaryoblastic, Acute / pathology
  • Leukemia, Megakaryoblastic, Acute / physiopathology*
  • Mitogens / pharmacology*
  • Molecular Sequence Data
  • Oligonucleotides, Antisense
  • Protein Serine-Threonine Kinases / physiology*
  • Proto-Oncogene Proteins / physiology*
  • Proto-Oncogene Proteins c-raf
  • Recombinant Proteins / pharmacology
  • Stem Cell Factor
  • Tumor Cells, Cultured

Substances

  • Codon
  • Growth Substances
  • Hematopoietic Cell Growth Factors
  • Interleukin-3
  • Interleukin-9
  • Mitogens
  • Oligonucleotides, Antisense
  • Proto-Oncogene Proteins
  • Recombinant Proteins
  • Stem Cell Factor
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-raf