Anti-Fas antibody induces different types of cell death in the human histiocytic cell line, U937, and the human B cell line, B104: the role of single-strand DNA breaks and poly (ADP-ribosyl)ation in cell death

Cell Immunol. 1994 Jan;153(1):184-93. doi: 10.1006/cimm.1994.1016.

Abstract

We investigated the anti-Fas antibody-induced cell death in two different types of human cell lines, U937 and B104. IFN-gamma increased the surface expression of Fas antigen and susceptibility to anti-Fas Ab-induced cell death of B104 and U937 cells. Anti-Fas Ab-induced death of U937 and B104 cells required neither a Ca2+ influx nor macromolecular synthesis. U937 cells treated with anti-Fas Ab represented apoptosis with DNA fragmentation, whereas anti-Fas Ab-treated B104 cells did not. Single-strand DNA breaks, however, appeared in the B104 cells. Zinc ions prevented DNA fragmentation and the morphological features of apoptosis in anti-Fas Ab-treated U937 cells, but did not inhibit cell death. However, zinc ions, when used in combination with the poly(ADP-ribosyl)ation inhibitors, inhibited anti-Fas Ab-induced U937 cell death. The inhibitors by themselves did not inhibit anti-Fas Ab-induced U937 cell death, but did inhibit anti-Fas Ab-induced B104 cell death. A substantial decrease in NAD pools was observed in anti-Fas Ab-treated B104 and U937 cells in parallel with the increase of DNA strand breaks before cell death became apparent. These results suggest the involvement of single-strand DNA breaks and poly(ADP-ribosyl)ation in the mechanisms of anti-Fas Ab-induced U937 and B104 cell death.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Surface / physiology*
  • Apoptosis* / drug effects
  • B-Lymphocytes / cytology*
  • Calcium / metabolism
  • Cell Line
  • DNA Damage* / drug effects
  • Histiocytes / cytology*
  • Humans
  • Interferon-gamma / pharmacology
  • NAD / metabolism
  • Poly Adenosine Diphosphate Ribose / metabolism*
  • Zinc / pharmacology
  • fas Receptor

Substances

  • Antigens, Surface
  • fas Receptor
  • NAD
  • Poly Adenosine Diphosphate Ribose
  • Interferon-gamma
  • Zinc
  • Calcium