In vivo treatment with granulocyte colony-stimulating factor does not delay apoptosis in human neutrophils by increasing the expression of the vacuolar proton ATPase

J Investig Med. 2002 Jan;50(1):33-7. doi: 10.2310/6650.2002.33515.

Abstract

Background: Neutrophils die by apoptosis, and in vivo administration of granulocyte colony-stimulating factor (G-CSF) delays this apoptotic cell death. G-CSF administered in vitro correlates delayed apoptosis with upregulation of the vacuolar proton ATPase (v-ATPase). Because this enzyme requires assembly of membrane and cytosolic domains to function, we hypothesized that in vivo G-CSF would increase synthesis and assembly of v-ATPase components to delay apoptosis.

Methods: Volunteers received G-CSF for 5 days, and each had a paired control. Neutrophils were isolated from subjects before the first and after the fifth injection. Proteins from cytosol or plasma membrane or from whole cell lysates were resolved by SDS-polyacrylamide gel electrophoresis and immunoblotted with antibody to the 33kDa v-ATPase E subunit. Densitometry quantified immunoreactivity.

Results: No significant increase on the E subunit occurred between treated and control groups.

Conclusion: In vivo G-CSF does not increase the amount of v-ATPase in neutrophils. Although G-CSF in vivo delays apoptosis, the mechanism(s) by which this occurs is not known.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apoptosis / drug effects
  • Granulocyte Colony-Stimulating Factor / pharmacology*
  • Humans
  • Middle Aged
  • Neutrophils / cytology
  • Neutrophils / drug effects*
  • Neutrophils / enzymology
  • Recombinant Proteins
  • Vacuolar Proton-Translocating ATPases / blood

Substances

  • Recombinant Proteins
  • Granulocyte Colony-Stimulating Factor
  • Vacuolar Proton-Translocating ATPases