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Novel cell death program leads to neutrophil extracellular traps

The Journal of Cell Biology · 2007 · Vol. 176(2) · pp. 231–241
Tobias A. FuchsUlrike Abu AbedChristian GoosmannRobert HurwitzIlka SchulzeV. WahnYvette WeinrauchVolker BrinkmannArturo Zychlinsky

Abstract

Neutrophil extracellular traps (NETs) are extracellular structures composed of chromatin and granule proteins that bind and kill microorganisms. We show that upon stimulation, the nuclei of neutrophils lose their shape, and the eu- and heterochromatin homogenize. Later, the nuclear envelope and the granule membranes disintegrate, allowing the mixing of NET components. Finally, the NETs are released as the cell membrane breaks. This cell death process is distinct from apoptosis and necrosis and depends on the generation of reactive oxygen species (ROS) by NADPH oxidase. Patients with chronic granulomatous disease carry mutations in NADPH oxidase and cannot activate this cell-death pathway or make NETs. This novel ROS-dependent death allows neutrophils to fulfill their antimicrobial function, even beyond their lifespan.

Neutrophil, Myeloperoxidase and Oxidative MechanismsImmune cells in cancerImmune Response and InflammationBiologyChronic granulomatous diseaseNADPH oxidaseCell biologyExtracellularProgrammed cell deathNeutrophil extracellular trapsReactive oxygen speciesChromatinApoptosis

MeSH terms

AntibodiesCatalaseCell SurvivalChromatinCytoplasmic GranulesEnzyme InhibitorsGranulomatous Disease, ChronicHumansHydrogen PeroxideImmunity, InnateMicroscopy, ElectronNeutrophilsNuclear EnvelopeOnium CompoundsPhagocytosis
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