A comparison of signaling requirements for apoptosis of human B lymphocytes induced by the B cell receptor and CD95/Fas

J Immunol. 1998 Jul 1;161(1):168-74.

Abstract

To define how the signaling pathways that mediate the B cell receptor (BCR) death pathway differ from those responsible for CD95/Fas-mediated death, we compared the BCR and Fas death pathways in two human B cell lines, B104 and BJAB. Both BCR- and Fas-induced apoptosis are blocked by the peptide cysteine protease inhibitor benzyloxycarbonyl-Val-Ala-Asp-fluoromethylketone (ZVAD (mlz)), demonstrating a common requirement caspase activity. Despite this common characteristic, the ability of actinomycin D and cycloheximide to block BCR-induced apoptosis, but not apoptosis induced by Fas cross-linking, suggests that a major difference between these two pathways is their differential requirements for new gene and protein synthesis. BCR- and Fas-mediated apoptosis are both accompanied by activation of stress-activated protein kinase and p38 mitogen-activated protein kinase (MAPK). Activation of both stress-activated protein kinase and p38 MAPK was inhibited by ZVAD (mlz), suggesting the involvement of caspases. To determine the role of p38 MAPK activation in BCR- and Fas-induced apoptosis, we employed SB203580, a specific inhibitor of p38 MAPK. SB203580 inhibited BCR-induced apoptosis, but not apoptosis induced by cross-linking Fas. Furthermore, both actinomycin D and SB203580 inhibited BCR-induced, but not Fas-induced, activation of caspase. Collectively, these findings establish a role for p38 MAPK in BCR-induced apoptosis both upstream and downstream of caspase activity. The p38 MAPK pathway may function to regulate transcriptional or translational events that are critical for BCR-induced apoptosis.

Publication types

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

MeSH terms

  • Annexin A5 / metabolism
  • Antibodies, Anti-Idiotypic / pharmacology
  • Antibodies, Monoclonal / metabolism
  • Antibodies, Monoclonal / pharmacology
  • Apoptosis / immunology*
  • B-Lymphocyte Subsets / enzymology
  • B-Lymphocyte Subsets / immunology*
  • B-Lymphocyte Subsets / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinases / physiology
  • Cysteine Endopeptidases / drug effects
  • Cysteine Endopeptidases / metabolism
  • Cysteine Proteinase Inhibitors / pharmacology
  • Enzyme Activation / drug effects
  • Enzyme Activation / immunology
  • Humans
  • Immunoglobulin M / immunology
  • Immunoglobulin M / metabolism
  • Kinetics
  • Lymphoma, B-Cell
  • Mitogen-Activated Protein Kinases*
  • Protein Binding / immunology
  • Receptors, Antigen, B-Cell / physiology*
  • Signal Transduction / immunology*
  • Tumor Cells, Cultured
  • fas Receptor / immunology
  • fas Receptor / physiology*
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Annexin A5
  • Antibodies, Anti-Idiotypic
  • Antibodies, Monoclonal
  • Cysteine Proteinase Inhibitors
  • Immunoglobulin M
  • Receptors, Antigen, B-Cell
  • anti-IgM
  • fas Receptor
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Cysteine Endopeptidases