Alternative Fas-mediated cell death pathway is dependent on the different cleavage patterns of procaspase-8

Mol Cell Biochem. 2009 Nov;331(1-2):231-8. doi: 10.1007/s11010-009-0164-8. Epub 2009 Jun 12.

Abstract

It has been reported that mitochondria-independent or mitochondria-dependent (type I/II) Fas signaling pathways in leukemia cells depend on the amount of active caspase-8. However, Bid molecules, which could not be cleaved in type I cells, could be effectively cleaved by recombinant active caspase-8 in vitro. The cleavage of recombinant Bid by recombinant active caspase-8 could be blocked by anti-p10 and anti-p18 specific antibodies. Fas receptors could be similarly internalized into cytoplasm in type I and type II cells. Interestingly, p10 subunit of active caspase-8 could be detected in both type I and II cells, while p18 subunit of active caspase-8 could be detected only in type II cells but not in type I cells. These results demonstrated that p18 subunit was necessary for Bid cleavage and the mitochondria pathway might be dependent on the release of p18 subunit from active caspase-8.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / pharmacology
  • BH3 Interacting Domain Death Agonist Protein / metabolism
  • Caspase 8 / chemistry
  • Caspase 8 / metabolism*
  • Cell Death / drug effects
  • Cell Line, Tumor
  • Endocytosis / drug effects
  • Enzyme Activation / drug effects
  • Humans
  • Leukemia / metabolism
  • Leukemia / pathology
  • Protein Subunits / metabolism
  • Recombinant Proteins / metabolism
  • Signal Transduction* / drug effects
  • fas Receptor / metabolism*

Substances

  • Antibodies
  • BH3 Interacting Domain Death Agonist Protein
  • FAS protein, human
  • Protein Subunits
  • Recombinant Proteins
  • fas Receptor
  • Caspase 8