4.7 Article

Activation of caspase-1 by the NLRP3 inflammasome regulates the NADPH oxidase NOX2 to control phagosome function

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NATURE IMMUNOLOGY
卷 14, 期 6, 页码 543-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/ni.2595

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资金

  1. US National Institutes of Health
  2. National Institute of Allergy and Infectious Diseases [RO1 AI079198, RO1 AI093752]
  3. National Institutes of Health National Institute on Aging [RO1 AG020255]
  4. Crohns' and Colitis and Hood foundations
  5. National Institutes of Health National Institute of Diabetes and Digestive and Kidney Diseases [RO1 DK093695]
  6. Massachusetts General Hospital Executive Committee on Research
  7. New England Regional Center of Excellence-Biodefense and Emerging Infectious Diseases [U54 AI057159]
  8. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [U54AI057159, R01AI093752, R01AI079198] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK093695, P30DK043351] Funding Source: NIH RePORTER
  10. NATIONAL INSTITUTE ON AGING [R01AG020255] Funding Source: NIH RePORTER

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Phagocytosis is a fundamental cellular process that is pivotal for immunity as it coordinates microbial killing, innate immune activation and antigen presentation. An essential step in this process is phagosome acidification, which regulates many functions of these organelles that allow phagosomes to participate in processes that are essential to both innate and adaptive immunity. Here we report that acidification of phagosomes containing Gram-positive bacteria is regulated by the NLRP3 inflammasome and caspase-1. Active caspase-1 accumulates on phagosomes and acts locally to control the pH by modulating buffering by the NADPH oxidase NOX2. These data provide insight into a mechanism by which innate immune signals can modify cellular defenses and establish a new function for the NLRP3 inflammasome and caspase-1 in host defense.

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