Novel cell death program leads to neutrophil extracellular traps

Tobias A. Fuchs(New York University), Ulrike Abu Abed(Core Laboratories (United States)), Christian Goosmann(Core Laboratories (United States)), Robert Hurwitz(Max Planck Institute for Infection Biology), Ilka Schulze(Charité - Universitätsmedizin Berlin), V. Wahn(Charité - Universitätsmedizin Berlin), Yvette Weinrauch(New York University), Volker Brinkmann(Core Laboratories (United States)), Arturo Zychlinsky
The Journal of Cell Biology
January 8, 2007
Cited by 3,126Open Access
Full Text

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.


Related Papers

No related papers found

Powered by citation graph analysis