1. Academic Validation
  2. The NLRP1 and CARD8 inflammasomes

The NLRP1 and CARD8 inflammasomes

  • Immunol Rev. 2020 Sep;297(1):13-25. doi: 10.1111/imr.12884.
Cornelius Y Taabazuing 1 Andrew R Griswold 2 3 Daniel A Bachovchin 1 4 3
Affiliations

Affiliations

  • 1 Chemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • 2 Weill Cornell, Rockefeller, Sloan Kettering Tri-Institutional MD-PhD Program, New York, NY, USA.
  • 3 Pharmacology Program of the Weill Cornell Graduate School of Medical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • 4 Tri-Institutional PhD Program in Chemical Biology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Abstract

Inflammasomes are multiprotein complexes that activate inflammatory cytokines and induce Pyroptosis in response to intracellular danger-associated signals. NLRP1 and CARD8 are related germline-encoded Pattern Recognition Receptors that form inflammasomes, but their activation mechanisms and biological purposes have not yet been fully established. Both NLRP1 and CARD8 undergo post-translational autoproteolysis to generate two non-covalently associated polypeptide chains. NLRP1 and CARD8 activators induce the proteasome-mediated destruction of the N-terminal fragment, liberating the C-terminal fragment to form an inflammasome. Here, we review the danger-associated stimuli that have been reported to activate NLRP1 and/or CARD8, including anthrax lethal toxin, Toxoplasma gondii, Shigella flexneri and the small molecule DPP8/9 inhibitor Val-boroPro, focusing on recent mechanistic insights and highlighting unresolved questions. In addition, we discuss the recently identified disease-associated mutations in NLRP1 and CARD8, the potential role that DPP9's protein structure plays in inflammasome regulation, and the emerging link between NLRP1 and metabolism. Finally, we summarize all of this latest research and consider the possible biological purposes of these enigmatic inflammasomes.

Keywords

CARD8; DPP8/9; NLRP1; Val-boroPro; anthrax lethal toxin; inflammasome; proteasome; pyroptosis.

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