The adaptor ASC has extracellular and 'prionoid' activities that propagate inflammation

Bernardo S. Franklin, Lukas Bossaller, Dominic De Nardo, Jacqueline M. Ratter, Andrea Stutz, Gudrun Engels, Christoph Brenker, Mark Nordhoff, Sandra R. Mirandola, Ashraf Al-Amoudi, Matthew S. Mangan, Sebastian Zimmer, Brian G. Monks, Martin Fricke, Reinhold E. Schmidt, Terje Espevik, Bernadette Jones, Andrew G. Jarnicki, Philip M. Hansbro, Patricia BustoAnn Marshak-Rothstein, Simone Hornemann, Adriano Aguzzi, Wolfgang Kastenmüller, Eicke Latz

Research output: Contribution to journalArticleResearchpeer-review

390 Citations (Scopus)

Abstract

Microbes or danger signals trigger inflammasome sensors, which induce polymerization of the adaptor ASC and the assembly of ASC specks. ASC specks recruit and activate caspase-1, which induces maturation of the cytokine interleukin 1β (IL-1β) and pyroptotic cell death. Here we found that after pyroptosis, ASC specks accumulated in the extracellular space, where they promoted further maturation of IL-1β. In addition, phagocytosis of ASC specks by macrophages induced lysosomal damage and nucleation of soluble ASC, as well as activation of IL-1β in recipient cells. ASC specks appeared in bodily fluids from inflamed tissues, and autoantibodies to ASC specks developed in patients and mice with autoimmune pathologies. Together these findings reveal extracellular functions of ASC specks and a previously unknown form of cell-to-cell communication.

Original languageEnglish
Pages (from-to)727-737
Number of pages11
JournalNature Immunology
Volume15
Issue number8
DOIs
Publication statusPublished - 22 Jun 2014
Externally publishedYes

Keywords

  • innate immunity

Cite this