Programmed cell death mediated by ced-3 and ced-4 protects Caenorhabditis elegans from Salmonella typhimurium-mediated killing

Proc Natl Acad Sci U S A. 2001 Feb 27;98(5):2735-9. doi: 10.1073/pnas.041613098. Epub 2001 Feb 13.

Abstract

Programmed cell death (PCD) in mammals has been implicated in several disease states including cancer, autoimmune disease, and neurodegenerative disease. In Caenorhabditis elegans, PCD is a normal component of development. We find that Salmonella typhimurium colonization of the C. elegans intestine leads to an increased level of cell death in the worm gonad. S. typhimurium-mediated germ-line cell death is not observed in C. elegans ced-3 and ced-4 mutants in which developmentally regulated cell death is blocked, and ced-3 and ced-4 mutants are hypersensitive to S. typhimurium-mediated killing. These results suggest that PCD may be involved in the C. elegans defense response to pathogen attack.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Apoptosis / genetics*
  • Caenorhabditis elegans / cytology
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans Proteins*
  • Calcium-Binding Proteins / genetics
  • Calcium-Binding Proteins / physiology*
  • Caspases / genetics
  • Caspases / physiology*
  • Germ Cells
  • Helminth Proteins / genetics
  • Helminth Proteins / physiology*
  • Mutation
  • Repressor Proteins / genetics
  • Salmonella typhimurium / pathogenicity*

Substances

  • Caenorhabditis elegans Proteins
  • Calcium-Binding Proteins
  • Ced-4 protein, C elegans
  • EGL-1 protein, C elegans
  • Helminth Proteins
  • Repressor Proteins
  • Caspases
  • ced-3 protein, C elegans