G-CSF signaling can differentiate promyelocytes expressing a defective retinoic acid receptor: evidence for divergent pathways regulating neutrophil differentiation

Blood. 2004 Mar 1;103(5):1693-701. doi: 10.1182/blood-2002-10-3247. Epub 2003 Nov 6.

Abstract

Several lines of investigation suggest that granulocyte colony-stimulating factor (G-CSF) augments all-trans retinoic acid (ATRA)-induced neutrophil differentiation in acute promyelocytic leukemia (APL). We sought to characterize the relationship between G-CSF- and ATRA-mediated neutrophil differentiation. We established a G-CSF receptor-transduced promyelocytic cell line, EPRO-Gr, derived from the granulocyte-macrophage colony-stimulating factor (GM-CSF)-dependent EPRO cell line harboring a dominant-negative retinoic acid receptor alpha (RARalpha). In EPRO-Gr, neutrophil differentiation occurs either in GM-CSF upon addition of ATRA or upon induction with G-CSF alone. Transient transfection of EPRO-Gr cells with a RARE-containing reporter plasmid demonstrates increased activity in the presence of ATRA, but not G-CSF, while STAT3 phosphorylation occurs only in response to G-CSF. This suggests that ATRA-mediated differentiation of EPRO-Gr cells occurs via a RARE-dependent, STAT3-independent pathway, while G-CSF-mediated differentiation occurs via a RARE-independent, STAT3-dependent pathway. ATRA and G-CSF thus regulate differentiation by divergent pathways. We characterized these pathways in the APL cell line, NB4. ATRA induction of NB4 cells resulted in morphologic differentiation and up-regulation of C/EBPepsilon and G-CSFR, but not in STAT3 phosphorylation. The addition of G-CSF with ATRA during NB4 induction resulted in STAT3 phosphorylation but did not enhance differentiation. These results may elucidate how G-CSF and ATRA affect the differentiation of primary and ATRA-resistant APL cells.

Publication types

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

MeSH terms

  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Cell Differentiation
  • Cell Division
  • Cell Line
  • Cell Line, Tumor
  • Cell Survival
  • Chromatin / metabolism
  • DNA-Binding Proteins / metabolism
  • Genes, Reporter
  • Granulocyte Colony-Stimulating Factor / metabolism*
  • Granulocyte Precursor Cells / cytology*
  • Granulocyte-Macrophage Colony-Stimulating Factor / metabolism
  • Humans
  • Luciferases / metabolism
  • Mice
  • Neutrophils / cytology*
  • Neutrophils / metabolism
  • Phosphorylation
  • Plasmids / metabolism
  • Precipitin Tests
  • Receptors, Retinoic Acid / genetics*
  • Receptors, Retinoic Acid / metabolism
  • Receptors, Retinoic Acid / physiology
  • Response Elements
  • Retinoic Acid Receptor alpha
  • Retroviridae / genetics
  • STAT3 Transcription Factor
  • Signal Transduction*
  • Time Factors
  • Trans-Activators / metabolism
  • Transfection
  • Up-Regulation

Substances

  • Chromatin
  • DNA-Binding Proteins
  • RARA protein, human
  • Rara protein, mouse
  • Receptors, Retinoic Acid
  • Retinoic Acid Receptor alpha
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Stat3 protein, mouse
  • Trans-Activators
  • Granulocyte Colony-Stimulating Factor
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Luciferases