IL-3 withdrawal activates a CrmA-insensitive poly(ADP-ribose) polymerase cleavage enzyme in factor-dependent myeloid progenitor cells

Leukemia. 1998 May;12(5):682-9. doi: 10.1038/sj.leu.2400992.

Abstract

Murine myeloid progenitor cells that are dependent on interleukin-3 (IL-3) undergo apoptosis when this essential cytokine is withdrawn. To determine whether IL-3 withdrawal leads to the activation of caspase proteases, known mediators of apoptosis, we studied proteolytic cleavage of the caspase substrate protein poly(ADP-ribose) polymerase (PARP) in two IL3-dependent myeloid progenitor cell lines, 32D and FDCP-1. We observed that IL-3 withdrawal leads to PARP cleavage in both cell lines, with complete cleavage occurring by 24 h after cytokine removal. The induced PARP cleavage activities were blocked by the caspase inhibitors z-DEVD-fluoromethyl ketone (z-DEVD-FMK) and z-VAD-fluoromethyl ketone (z-VAD-FMK), or by overexpression in 32D cells of Bcl-2 or BCR/ABL. By contrast, overexpression in 32D cells of cowpox virus CrmA protein, an inhibitor of Fas-mediated PARP cleavage, failed to inhibit PARP cleavage following IL-3 withdrawal. CrmA also failed to block DNA fragmentation and loss of cell viability. We propose that a CrmA-insensitive caspase protease is activated in the IL-3-deprived myeloid precursors, and that activation of this protease may direct the cells on a path towards commitment to death.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Cells, Cultured
  • DNA / drug effects
  • DNA / metabolism
  • Enzyme Activation
  • Hematopoietic Stem Cells / enzymology*
  • Interleukin-3 / pharmacology*
  • Mice
  • Poly(ADP-ribose) Polymerase Inhibitors
  • Poly(ADP-ribose) Polymerases / metabolism*
  • Protease Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / physiology
  • Sensitivity and Specificity
  • Serpins / biosynthesis
  • Serpins / genetics
  • Serpins / physiology*
  • Substance Withdrawal Syndrome / enzymology*
  • Substance Withdrawal Syndrome / etiology
  • Transfection
  • Viral Proteins*

Substances

  • Interleukin-3
  • Poly(ADP-ribose) Polymerase Inhibitors
  • Protease Inhibitors
  • Proto-Oncogene Proteins c-bcl-2
  • Serpins
  • Viral Proteins
  • DNA
  • interleukin-1beta-converting enzyme inhibitor
  • Poly(ADP-ribose) Polymerases