Differential sensitivity of Jurkat and primary T cells to caspase-independent cell death triggered upon Fas stimulation

Eur J Immunol. 2002 Aug;32(8):2376-84. doi: 10.1002/1521-4141(200208)32:8<2376::AID-IMMU2376>3.0.CO;2-V.

Abstract

Fas-induced apoptosis, a key event in the regulation of lymphocyte homeostasis, is mainly mediated by the activation of a cascade of caspases. Using caspase- and Fas-associated death domain protein-deficient Jurkat cell lines as well as a pan-caspase inhibitor (Z-VAD-fmk), we observed a second Fas-induced cell death event, independent of any known caspase activation. This pathway is of slow kinetics and displays some features of necrosis. However, this caspase-independent pathway does not seem to play a significant role in the Fas-mediated death of primary activated T cell blasts. Indeed, in this setting, Fas-induced cell death was always substantially inhibited by Z-VAD-fmk, suggesting that caspase activation is an absolute requirement in the Fas-induced death of primary human T lymphocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis*
  • Caspases / physiology*
  • Humans
  • Jurkat Cells
  • Kinetics
  • Lymphocyte Activation
  • T-Lymphocytes / physiology*
  • fas Receptor / physiology*

Substances

  • fas Receptor
  • Caspases