Novel cell death program leads to neutrophil extracellular traps

Author:

Fuchs Tobias A.12,Abed Ulrike13,Goosmann Christian13,Hurwitz Robert4,Schulze Ilka5,Wahn Volker5,Weinrauch Yvette2,Brinkmann Volker3,Zychlinsky Arturo1

Affiliation:

1. Department for Cellular Microbiology

2. Department of Microbiology, New York University School of Medicine, New York, NY 10016

3. Microscopy Core Facility,

4. Protein Purification Core Facility, Max-Planck Institute for Infection Biology, 10117 Berlin, Germany

5. Department for Paediatric Pneumology and Immunology, Charité Universitätsmedizin Berlin, 13353 Berlin, Germany

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.

Publisher

Rockefeller University Press

Subject

Cell Biology

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