The protein kinase PKR is required for macrophage apoptosis after activation of Toll-like receptor 4

Nature. 2004 Mar 18;428(6980):341-5. doi: 10.1038/nature02405.


Macrophages are pivotal constituents of the innate immune system, vital for recognition and elimination of microbial pathogens. Macrophages use Toll-like receptors (TLRs) to detect pathogen-associated molecular patterns--including bacterial cell wall components, such as lipopolysaccharide or lipoteichoic acid, and viral nucleic acids, such as double-stranded (ds)RNA--and in turn activate effector functions, including anti-apoptotic signalling pathways. Certain pathogens, however, such as Salmonella spp., Shigellae spp. and Yersiniae spp., use specialized virulence factors to overcome these protective responses and induce macrophage apoptosis. We found that the anthrax bacterium, Bacillus anthracis, selectively induces apoptosis of activated macrophages through its lethal toxin, which prevents activation of the anti-apoptotic p38 mitogen-activated protein kinase. We now demonstrate that macrophage apoptosis by three different bacterial pathogens depends on activation of TLR4. Dissection of anti- and pro-apoptotic signalling events triggered by TLR4 identified the dsRNA responsive protein kinase PKR as a critical mediator of pathogen-induced macrophage apoptosis. The pro-apoptotic actions of PKR are mediated both through inhibition of protein synthesis and activation of interferon response factor 3.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis* / drug effects
  • Bacillus anthracis / physiology
  • Cells, Cultured
  • DNA-Binding Proteins / metabolism
  • Gene Deletion
  • Interferon Regulatory Factor-3
  • Lipopolysaccharides / pharmacology
  • Macrophages / cytology*
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Macrophages / microbiology
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Receptors, Cell Surface / metabolism*
  • Salmonella typhimurium / physiology
  • Signal Transduction / drug effects
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • Transcription Factors / metabolism
  • Yersinia pseudotuberculosis / physiology
  • eIF-2 Kinase / deficiency
  • eIF-2 Kinase / genetics
  • eIF-2 Kinase / metabolism*


  • DNA-Binding Proteins
  • Interferon Regulatory Factor-3
  • Irf3 protein, mouse
  • Lipopolysaccharides
  • Membrane Glycoproteins
  • Receptors, Cell Surface
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • Transcription Factors
  • eIF-2 Kinase