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Bacterial RNA and small antiviral compounds activate caspase-1 through cryopyrin/Nalp3

Author

Listed:
  • Thirumala-Devi Kanneganti

    (University of Michigan Medical School)

  • Nesrin Özören

    (University of Michigan Medical School)

  • Mathilde Body-Malapel

    (University of Michigan Medical School)

  • Amal Amer

    (University of Michigan Medical School)

  • Jong-Hwan Park

    (University of Michigan Medical School)

  • Luigi Franchi

    (University of Michigan Medical School)

  • Joel Whitfield

    (University of Michigan Medical School)

  • Winfried Barchet

    (Washington University School of Medicine)

  • Marco Colonna

    (Washington University School of Medicine)

  • Peter Vandenabeele

    (Ghent University)

  • John Bertin

    (Millennium Pharmaceuticals Inc.
    Synta Pharmaceuticals)

  • Anthony Coyle

    (Millennium Pharmaceuticals Inc.
    MedImmune Inc.)

  • Ethan P. Grant

    (Millennium Pharmaceuticals Inc.
    Synta Pharmaceuticals)

  • Shizuo Akira

    (Osaka University)

  • Gabriel Núñez

    (University of Michigan Medical School)

Abstract

The first line of defence The inflammasome is a complex of proteins involved in the activation of the innate immune system, an evolutionarily ancient antimicrobial defence found in most multicelled animals. When activated the inflammasome sets in motion a cascade of events that leads to the production of active molecules including interleukins. Three papers in this issue report the identification of endogenous danger signals and bacterial components that activate inflammasomes containing cryopyrin (also known as NALP3). Mariathasan et al. show that cryopyrin activates the inflammasome in response to bacterial toxins and to ATP. Kanneganti et al. show that cryopyrin is activated by bacterial RNA and by the immune response modifiers R837 and R848. And Martinon et al. show that gout-associated uric acid crystals have a similar effect. In sum these results show that cryopyrin has a vital role in host antibacterial defences and may act as a sensor of cellular stress. In addition, this work provides insight into the mechanisms of autoinflammatory disorders in which abnormalities in the innate immune system have been implicated.

Suggested Citation

  • Thirumala-Devi Kanneganti & Nesrin Özören & Mathilde Body-Malapel & Amal Amer & Jong-Hwan Park & Luigi Franchi & Joel Whitfield & Winfried Barchet & Marco Colonna & Peter Vandenabeele & John Bertin & , 2006. "Bacterial RNA and small antiviral compounds activate caspase-1 through cryopyrin/Nalp3," Nature, Nature, vol. 440(7081), pages 233-236, March.
  • Handle: RePEc:nat:nature:v:440:y:2006:i:7081:d:10.1038_nature04517
    DOI: 10.1038/nature04517
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    Cited by:

    1. Joo-Hui Han & Rajendra Karki & R. K. Subbarao Malireddi & Raghvendra Mall & Roman Sarkar & Bhesh Raj Sharma & Jonathon Klein & Harmut Berns & Harshan Pisharath & Shondra M. Pruett-Miller & Sung-Jin Ba, 2024. "NINJ1 mediates inflammatory cell death, PANoptosis, and lethality during infection conditions and heat stress," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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