NLRP3 inflammasome activation downstream of cytoplasmic LPS recognition by both caspase-4 and caspase-5

Eur J Immunol. 2015 Oct;45(10):2918-26. doi: 10.1002/eji.201545655. Epub 2015 Aug 24.

Abstract

Humans encode two inflammatory caspases that detect cytoplasmic LPS, caspase-4 and caspase-5. When activated, these trigger pyroptotic cell death and caspase-1-dependent IL-1β production; however the mechanism underlying this process is not yet confirmed. We now show that a specific NLRP3 inhibitor, MCC950, prevents caspase-4/5-dependent IL-1β production elicited by transfected LPS. Given that both caspase-4 and caspase-5 can detect cytoplasmic LPS, it is possible that these proteins exhibit some degree of redundancy. Therefore, we generated human monocytic cell lines in which caspase-4 and caspase-5 were genetically deleted either individually or together. We found that the deletion of caspase-4 suppressed cell death and IL-1β production following transfection of LPS into the cytoplasm, or in response to infection with Salmonella typhimurium. Although deletion of caspase-5 did not confer protection against transfected LPS, cell death and IL-1β production were reduced after infection with Salmonella. Furthermore, double deletion of caspase-4 and caspase-5 had a synergistic effect in the context of Salmonella infection. Our results identify the NLRP3 inflammasome as the specific platform for IL-1β maturation, downstream of cytoplasmic LPS detection by caspase-4/5. We also show that both caspase-4 and caspase-5 are functionally important for appropriate responses to intracellular Gram-negative bacteria.

Keywords: Caspase-4; Caspase-5; LPS; NLRP3 inflammasome; Pyroptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / immunology*
  • Caspases / immunology*
  • Caspases, Initiator / immunology*
  • Cell Line, Tumor
  • Humans
  • Interleukin-1beta / immunology
  • Lipopolysaccharides / immunology*
  • Monocytes / immunology*
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Salmonella Infections / immunology*
  • Salmonella typhimurium / immunology*

Substances

  • Carrier Proteins
  • IL1B protein, human
  • Interleukin-1beta
  • Lipopolysaccharides
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • NLRP3 protein, human
  • CASP4 protein, human
  • CASP5 protein, human
  • Caspases
  • Caspases, Initiator