Enhancement of interleukin-3-dependent mast cell proliferation by suppression of c-jun expression

J Biol Chem. 1994 Mar 18;269(11):8498-503.

Abstract

We have previously shown that protein kinase C (PKC) depletion is associated with an increase in the proliferation of interleukin 3 (IL-3)-induced mast cells. Here we show that the AP-1 components c-Jun and c-Fos are induced by IL-3. While c-Jun's induction by IL-3 is totally dependent on PKC, c-Fos induction by IL-3 is only attenuated by PKC depletion. AP-1 binding activity was also induced by IL-3 but this induction was PKC independent. These results indicated a possible involvement of c-Jun in the inhibition of IL-3-induced growth regulation. A support for this assumption came from experiments in which an increase in thymidine incorporation into mast cells was noted when c-jun antisense oligomers were administered to IL-3-treated cells. Since the only known effect of direct inhibition of c-Jun on proliferation rates in several cellular systems was a reduction of proliferation, we verified that our c-jun antisense oligomer could also inhibit proliferation rates in fibroblasts where such a repression was previously reported. Thus c-Jun has an inhibitory effect on IL-3 induction of mast cells proliferation that is distinct from its role in several other cellular environments. These observations reveal the involvement of AP-1 and its components in IL-3-induced signal transduction and the importance of the mast cell environment in determining their specific cellular function.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Division / drug effects
  • Cell Line
  • DNA / biosynthesis
  • DNA Primers
  • DNA Probes
  • Gene Expression / drug effects*
  • Genes, jun / drug effects
  • Interleukin-3 / pharmacology*
  • Kinetics
  • Liver / metabolism
  • Mast Cells / cytology*
  • Mast Cells / drug effects
  • Mast Cells / metabolism*
  • Mice
  • Molecular Sequence Data
  • Oligonucleotides, Antisense / pharmacology
  • Protein Kinase C / metabolism*
  • Proto-Oncogene Proteins c-fos / biosynthesis
  • Proto-Oncogene Proteins c-fos / isolation & purification
  • Proto-Oncogene Proteins c-jun / antagonists & inhibitors
  • Proto-Oncogene Proteins c-jun / biosynthesis*
  • Proto-Oncogene Proteins c-jun / isolation & purification
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / metabolism
  • Thymidine / metabolism

Substances

  • DNA Primers
  • DNA Probes
  • Interleukin-3
  • Oligonucleotides, Antisense
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • RNA, Messenger
  • DNA
  • Protein Kinase C
  • Thymidine