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      Requirement of an ICE/CED-3 protease for Fas/APO-1-mediated apoptosis.

      Nature
      Amino Acid Sequence, Animals, Antigens, CD95, Antigens, Surface, physiology, Apoptosis, Base Sequence, Caenorhabditis elegans Proteins, Caspase 1, Caspases, Cell Line, Cysteine Endopeptidases, DNA, Antisense, metabolism, Enzyme Activation, Helminth Proteins, Mice, Molecular Sequence Data, Serpins, Transfection, Viral Proteins

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          Abstract

          The Fas/APO-1 receptor is one of the major regulators of apoptosis. We report here that Fas/APO-1-mediated apoptosis requires the activation of a new class of cysteine proteases, including interleukin-1 beta-converting enzyme (ICE), which are homologous to the product of the Caenorhabditis elegans cell-death gene ced-3 (refs 11, 12). Triggering of Fas/APO-1 rapidly stimulated the proteolytic activity of ICE. Overexpression of ICE, achieved by electroporation and microinjection, strongly potentiated Fas/APO-1-mediated cell death. In addition, inhibition of ICE activity by protease inhibitors, as well as by transient expression of the pox virus-derived serpin inhibitor CrmA or an antisense ICE construct, substantially suppressed Fas/APO-1-triggered cell death. We conclude that activation of ICE or an ICE-related protease is a critical event in Fas/APO-1-mediated cell death.

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