Novel cell death program leads to neutrophil extracellular traps

J Cell Biol. 2007 Jan 15;176(2):231-41. doi: 10.1083/jcb.200606027. Epub 2007 Jan 8.

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.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antibodies / pharmacology
  • Apoptosis / drug effects
  • Apoptosis / immunology
  • Apoptosis / physiology*
  • Catalase / antagonists & inhibitors
  • Catalase / pharmacology
  • Cell Death / drug effects
  • Cell Death / immunology
  • Cell Death / physiology
  • Cell Survival / drug effects
  • Cell Survival / immunology
  • Cell Survival / physiology
  • Chromatin / metabolism
  • Cytoplasmic Granules / metabolism
  • Cytoplasmic Granules / ultrastructure
  • Enzyme Inhibitors / pharmacology
  • Granulomatous Disease, Chronic / metabolism
  • Granulomatous Disease, Chronic / pathology
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Immunity, Innate / physiology*
  • Leukocyte Elastase / metabolism
  • Microscopy, Electron
  • NADPH Oxidases / antagonists & inhibitors
  • Neutrophil Activation / drug effects
  • Neutrophil Activation / physiology*
  • Neutrophils / cytology
  • Neutrophils / microbiology
  • Neutrophils / physiology*
  • Nuclear Envelope / metabolism
  • Nuclear Envelope / ultrastructure
  • Onium Compounds / pharmacology
  • Phagocytosis / immunology
  • Reactive Oxygen Species / metabolism
  • Staphylococcus aureus / physiology
  • Tetradecanoylphorbol Acetate / pharmacology
  • Vacuoles / metabolism
  • Vacuoles / ultrastructure
  • fas Receptor / immunology

Substances

  • Antibodies
  • Chromatin
  • Enzyme Inhibitors
  • Onium Compounds
  • Reactive Oxygen Species
  • fas Receptor
  • diphenyleneiodonium
  • Hydrogen Peroxide
  • Catalase
  • NADPH Oxidases
  • Leukocyte Elastase
  • Tetradecanoylphorbol Acetate