Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization

• DOI: 10.1038/ni.1631
• Publication Date: 2008-07-06T19:16:23Z
• Authors: Veit Hornung; Franz Bauernfeind; Annett Halle; Eivind O Samstad; Hajime Kono; Kenneth L Rock; Katherine A Fitzg...; Eicke Latz
• Keywords: Inflammation; 0303 health sciences; Macrophages; Silicosis; 610; Inbred C57BL; 540; Silicon Dioxide; Mice, Inbred C57BL; Mice; 03 medical and health sciences; NLR Family, Pyrin Domain-Containing 3 Protein; Animals; Inflammation Mediators; Aluminum Compounds; Carrier Proteins; Immunology and Infectious Disease

Inhalation of silica crystals causes inflammation in the alveolar space. Prolonged exposure to silica can lead to the development of silicosis, an irreversible, fibrotic pulmonary disease. The mechanisms by which silica and other crystals activate immune cells are not well understood. Here we demonstrate that silica and aluminum salt crystals activated inflammasomes formed by the cytoplasmic receptor NALP3. NALP3 activation required phagocytosis of crystals, and this uptake subsequently led to lysosomal damage and rupture. 'Sterile' lysosomal damage (without crystals) also induced NALP3 activation, and inhibition of either phagosomal acidification or cathepsin B activity impaired NALP3 activation. Our results indicate that the NALP3 inflammasome senses lysosomal damage as an endogenous 'danger' signal.