NLRP1- A CINDERELLA STORY: a perspective of recent advances in NLRP1 and the questions they raise.

Kristian Barry, Christopher Murphy, Ashley Mansell
Author Information
  1. Kristian Barry: Centre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Clayton, VIC, Australia.
  2. Christopher Murphy: 7 Warren St., Upton, MA, 01568, USA.
  3. Ashley Mansell: Centre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Clayton, VIC, Australia. ashley.mansell@hudson.org.au. ORCID

Abstract

NLRP1, while the first inflammasome described, has only recently begun to gain significant attention in disease pathology, inflammation research, and potentially, as a therapeutic target. Recently identified human variants provide key insights into NLRP1 biology while its unique expression in barrier cells such as keratinocytes and airway epithelial cells has aligned with new, human specific agonists. This differentiates NLRP1 from other inflammasomes such as NLRP3 and identifies it as a key therapeutic target in inflammatory diseases. Indeed, recent discoveries highlight that NLRP1 may be the predominant inflammasome in human barrier cells, its primary role akin to NLRP3, to respond to cellular stress. This review focuses on recent studies identifying new human-specific NLRP1 mechanisms of activation of, gain-of-function human variants and disease, its role in responding to cellular stress, and discuss potential advances and the therapeutic potential for NLRP1.

References

  1. Proc Natl Acad Sci U S A. 2023 Jan 31;120(5):e2213777120 [PMID: 36693106]
  2. Cell. 2016 Sep 22;167(1):187-202.e17 [PMID: 27662089]
  3. J Exp Med. 2023 Jan 2;220(1): [PMID: 36315050]
  4. J Histochem Cytochem. 2007 May;55(5):443-52 [PMID: 17164409]
  5. Cell Rep. 2023 Jan 31;42(1):111965 [PMID: 36649711]
  6. Sci Rep. 2017 Jun 16;7(1):3715 [PMID: 28623311]
  7. J Biol Chem. 2022 Dec;298(12):102645 [PMID: 36309085]
  8. Science. 2019 Apr 5;364(6435): [PMID: 30872533]
  9. Science. 2021 Jan 29;371(6528): [PMID: 33243852]
  10. Nat Med. 2018 Aug;24(8):1151-1156 [PMID: 29967349]
  11. Curr Biol. 2007 Jul 3;17(13):1140-5 [PMID: 17600714]
  12. Cell Rep. 2023 Jan 31;42(1):111966 [PMID: 36649710]
  13. Br J Dermatol. 2023 Feb 10;188(2):259-267 [PMID: 36763876]
  14. Nature. 2021 Apr;592(7856):778-783 [PMID: 33731932]
  15. Proc Natl Acad Sci U S A. 2019 Sep 17;116(38):19055-19063 [PMID: 31484767]
  16. Cell Death Dis. 2019 Aug 5;10(8):587 [PMID: 31383852]
  17. Sci Immunol. 2022 Sep 16;7(75):eabi4611 [PMID: 36112693]
  18. PLoS One. 2011;6(11):e27396 [PMID: 22087307]
  19. J Invest Dermatol. 2018 Dec;138(12):2644-2652 [PMID: 30096351]
  20. Cell Death Dis. 2020 Aug 14;11(8):628 [PMID: 32796818]
  21. J Exp Med. 2023 Oct 2;220(10): [PMID: 37642996]
  22. Nat Commun. 2021 Jan 8;12(1):188 [PMID: 33420028]
  23. Cell Microbiol. 2008 Jun;10(6):1352-62 [PMID: 18266992]
  24. Elife. 2021 Jan 07;10: [PMID: 33410748]
  25. Clin Transl Immunology. 2023 Jun 22;12(6):e1455 [PMID: 37360982]
  26. Br J Dermatol. 2014 Dec;171(6):1517-20 [PMID: 24909542]
  27. EMBO J. 2020 Oct 1;39(19):e105071 [PMID: 32840892]
  28. Cell Death Dis. 2021 Jan 11;12(1):57 [PMID: 33431827]
  29. Rheumatology (Oxford). 2020 Sep 1;59(9):2334-2339 [PMID: 31873740]
  30. Nucleic Acids Res. 2020 Nov 4;48(19):10648-10661 [PMID: 32941609]
  31. Cell Stress. 2021 May 03;5(6):86-88 [PMID: 34124583]
  32. Immunity. 2011 May 27;34(5):629-36 [PMID: 21616433]
  33. N Engl J Med. 2007 Mar 22;356(12):1216-25 [PMID: 17377159]
  34. Science. 2022 Jul 15;377(6603):328-335 [PMID: 35857590]
  35. Immunity. 2011 May 27;34(5):637-50 [PMID: 21616434]
  36. Cell Death Dis. 2018 Jan 18;9(2):24 [PMID: 29348630]
  37. Nature. 2023 Oct;622(7981):188-194 [PMID: 37704723]
  38. PLoS Pathog. 2013;9(6):e1003452 [PMID: 23818853]
  39. J Allergy Clin Immunol. 2023 Nov;152(5):1336-1344.e5 [PMID: 37544411]
  40. J Allergy Clin Immunol. 2021 Jun;147(6):2134-2145.e20 [PMID: 33378691]
  41. Nat Commun. 2021 Mar 5;12(1):1461 [PMID: 33674575]
  42. Nat Genet. 2006 Feb;38(2):240-4 [PMID: 16429160]
  43. Nat Chem Biol. 2017 Jan;13(1):46-53 [PMID: 27820798]
  44. Nat Genet. 2018 Nov;50(11):1574-1583 [PMID: 30275530]
  45. J Biol Chem. 2007 Nov 23;282(47):34260-7 [PMID: 17878154]
  46. Ann Rheum Dis. 2017 Jul;76(7):1191-1198 [PMID: 27965258]
  47. Cell. 2020 Jul 23;182(2):404-416.e14 [PMID: 32610081]
  48. Mol Cell. 2002 Aug;10(2):417-26 [PMID: 12191486]
  49. J Exp Med. 2022 Oct 3;219(10): [PMID: 36129453]
  50. Curr Opin Immunol. 2023 Aug;83:102354 [PMID: 37311351]
  51. Pharmacol Rev. 2021 Jul;73(3):968-1000 [PMID: 34117094]
  52. Mol Cell. 2020 May 21;78(4):700-713.e7 [PMID: 32289254]
  53. Science. 2021 Mar 19;371(6535): [PMID: 33542150]
  54. J Exp Med. 2023 Oct 2;220(10): [PMID: 37642997]
  55. Immunol Rev. 2020 Sep;297(1):13-25 [PMID: 32558991]
  56. Sci Immunol. 2022 Nov 11;7(77):eabm7200 [PMID: 36332009]

MeSH Term

Humans
NLR Family, Pyrin Domain-Containing 3 Protein
Inflammasomes
Adaptor Proteins, Signal Transducing
NLR Proteins
Apoptosis Regulatory Proteins

Chemicals

NLR Family, Pyrin Domain-Containing 3 Protein
Inflammasomes
Adaptor Proteins, Signal Transducing
NLR Proteins
Apoptosis Regulatory Proteins
NLRP1 protein, human

Word Cloud

Created with Highcharts 10.0.0NLRP1humantherapeuticcellsrecentinflammasomediseasetargetvariantskeybarriernewNLRP3rolecellularstresspotentialadvancesfirstdescribedrecentlybegungainsignificantattentionpathologyinflammationresearchpotentiallyRecentlyidentifiedprovideinsightsbiologyuniqueexpressionkeratinocytesairwayepithelialalignedspecificagonistsdifferentiatesinflammasomesidentifiesinflammatorydiseasesIndeeddiscoverieshighlightmaypredominantprimaryakinrespondreviewfocusesstudiesidentifyinghuman-specificmechanismsactivationgain-of-functionrespondingdiscussNLRP1-CINDERELLASTORY:perspectivequestionsraise

Similar Articles

Cited By