Protein kinase C and c-myc gene activation pathways in thrombopoietin signal transduction

Biochem Biophys Res Commun. 1997 Feb 13;231(2):290-4. doi: 10.1006/bbrc.1996.5969.

Abstract

Thrombopoietin (TPO) is the major regulator of the proliferation and differentiation of megakaryocyte precursors through interaction with its receptor encoded by the c-mpl protooncogene. We established the human TPO-dependent leukemia cell line, UT-7/TPO (Blood 87, 4552, 1996). In these cells, TPO activated protein kinase C (PKC) in a time dependent manner. Subsequently, the c-myc gene was transiently induced to a maximal level 60-90 minutes after TPO exposure. In addition, we found that stimulating UT-7/TPO cells with TPO rapidly induces the significant accumulation of inositol 1, 4, 5-trisphosphate (Ins-P3), leading to the mobilization of calcium from intracellular stores. Taken together, the activation of PKC and subsequent c-myc gene induction are involved in the TPO-induced cellular response(s), presumably through the activation of PLC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / metabolism
  • Cell Line
  • Enzyme Activation
  • Gene Expression Regulation*
  • Genes, myc*
  • Humans
  • Inositol 1,4,5-Trisphosphate / biosynthesis
  • Isoenzymes / metabolism
  • Phospholipase C gamma
  • Phosphorylation
  • Protein Kinase C / metabolism*
  • Recombinant Proteins / metabolism
  • Signal Transduction*
  • Thrombopoietin / metabolism*
  • Transcriptional Activation
  • Type C Phospholipases / metabolism
  • Tyrosine / metabolism

Substances

  • Isoenzymes
  • Recombinant Proteins
  • Tyrosine
  • Inositol 1,4,5-Trisphosphate
  • Thrombopoietin
  • Protein Kinase C
  • Type C Phospholipases
  • Phospholipase C gamma
  • Calcium