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Related Experiment Video

Updated: Jun 9, 2026

High Throughput Measurement of Extracellular DNA Release and Quantitative NET Formation in Human Neutrophils In Vitro
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Extracellular DNA traps promote thrombosis.

Tobias A Fuchs1, Alexander Brill, Daniel Duerschmied

  • 1Immune Disease Institute, Boston, MA 02115, USA.

Proceedings of the National Academy of Sciences of the United States of America
|August 28, 2010
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Neutrophil extracellular traps (NETs) form a scaffold that promotes blood clot (thrombus) formation. Inhibiting NETs or histones prevents this, revealing a link between inflammation and thrombosis.

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Area of Science:

  • Immunology
  • Vascular Biology
  • Hematology

Background:

  • Neutrophil extracellular traps (NETs) are DNA-based structures involved in innate immunity.
  • NETs are increasingly recognized in non-infectious diseases and within the vasculature.

Purpose of the Study:

  • To investigate the role of NETs in thrombus formation.
  • To explore the mechanisms by which NETs contribute to thrombosis.

Main Methods:

  • Perfusing blood over NETs.
  • Using DNase and heparin to dismantle NETs.
  • Stimulating platelets with purified histones.
  • Analyzing thrombus composition and markers in vivo.

Main Results:

  • NETs induced platelet adhesion, activation, and aggregation.
  • DNase and heparin inhibited NET-induced thrombus formation.
  • Histones alone were sufficient to aggregate platelets.
  • NETs promoted red blood cell recruitment and fibrin deposition, forming red thrombi.
  • NET markers were detected in deep vein thrombosis models.

Conclusions:

  • NETs serve as a scaffold and stimulus for thrombus formation.
  • NETs represent a novel link between inflammation and thrombosis.
  • This finding may explain the association between infection and thrombosis.