APO-1 mediated apoptosis or proliferation in human chronic B lymphocytic leukemia: correlation with bcl-2 oncogene expression

Eur J Immunol. 1993 Mar;23(3):702-8. doi: 10.1002/eji.1830230320.

Abstract

We studied induction of apoptosis in several human malignant B cells from chronic lymphocytic leukemias (BCLL) by triggering the APO-1 antigen. The APO-1 antigen was found to be expressed on the surface of malignant B cells. In BCLL cells from most patients, APO-1 antigen expression increased following in vitro activation by Staphylococcus aureus Cowan I (SAC) or interleukin-2 (IL-2). In certain cases of BCLL co-stimulation with SAC plus IL-2 resulted in a synergistic up-regulation of the APO-1 antigen on the cell surface and prepared BCLL cells for monoclonal antibody anti-APO-1 mediated apoptosis. Interestingly, bcl-2 mRNA expression decreased upon stimulation with SAC plus IL-2, whereas SAC or IL-2 alone did not affect the level of bcl-2 expression. Thus, in these BCLL cells induction of anti-APO-1-mediated apoptosis appeared to be correlated with bcl-2 mRNA down-regulation. One informative BCLL, however, with a similar pattern of APO-1-antigen expression, did not show SAC plus IL-2-dependent bcl-2 down-regulation. Surprisingly, these cells proliferated in response to anti-APO-1 only when cells were co-stimulated with SAC plus IL-2. Our data suggest that down-regulation of bcl-2 prepares BCLL cells for induction of APO-1-mediated apoptosis. In addition they demonstrate that triggering of the APO-1 antigen may also lead to the induction of proliferation in special cases of BCLL.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Surface / physiology*
  • Apoptosis*
  • Base Sequence
  • Cell Division*
  • Gene Expression Regulation, Leukemic
  • Humans
  • In Vitro Techniques
  • Interleukin-2 / pharmacology
  • Leukemia, Lymphocytic, Chronic, B-Cell / physiopathology*
  • Lymphocyte Activation
  • Molecular Sequence Data
  • Oligodeoxyribonucleotides / chemistry
  • Oncogenes
  • Proto-Oncogene Proteins / physiology*
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger / genetics
  • Receptors, Cell Surface / physiology
  • Staphylococcus aureus / immunology
  • Tumor Cells, Cultured
  • Up-Regulation
  • fas Receptor

Substances

  • Antigens, Surface
  • Interleukin-2
  • Oligodeoxyribonucleotides
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger
  • Receptors, Cell Surface
  • fas Receptor