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Updated: Jun 21, 2025

Bioparticle Microarrays for Chemotactic and Molecular Analysis of Human Neutrophil Swarming in vitro
Published on: February 16, 2020
Neutrophil-derived migrasomes are an essential part of the coagulation system
Dong Jiang1, Lin Jiao2, Qing Li3
1State Key Laboratory of Membrane Biology, Tsinghua University-Peking University Joint Center for Life Sciences, Beijing Frontier Research Center for Biological Structure, School of Life Sciences, Tsinghua University, Beijing, China.
Abstract:
Migrasomes are organelles that are generated by migrating cells. Here we report the key role of neutrophil-derived migrasomes in haemostasis. We found that a large number of neutrophil-derived migrasomes exist in the blood of mice and humans. Compared with neutrophil cell bodies and platelets, these migrasomes adsorb and enrich coagulation factors on the surface. Moreover, they are highly enriched with adhesion molecules, which enable them to preferentially accumulate at sites of injury, where they trigger platelet activation and clot formation. Depletion of neutrophils, or genetic reduction of the number of these migrasomes, significantly decreases platelet plug formation and impairs coagulation. These defects can be rescued by intravenous injection of purified neutrophil-derived migrasomes. Our study reveals neutrophil-derived migrasomes as a previously unrecognized essential component of the haemostasis system, which may shed light on the cause of various coagulation disorders and open therapeutic possibilities.
Insights
Neutrophil-derived migrasomes play a crucial role in blood clotting (haemostasis). These tiny structures, found in blood, help form clots by attracting platelets and coagulation factors to injury sites.
Area of Science:
- Cell Biology
- Haematology
- Immunology
Background:
- Migrasomes are novel organelles produced by migrating cells.
- Their specific function in physiological processes remains largely unexplored.
- The role of neutrophils beyond immunity is an area of active investigation.
Purpose of the Study:
- To investigate the function of neutrophil-derived migrasomes in haemostasis.
- To determine if migrasomes contribute to blood clot formation.
- To explore the therapeutic potential of neutrophil migrasomes.
Main Methods:
- Detection and quantification of neutrophil-derived migrasomes in mouse and human blood.
- Biochemical analysis of migrasome composition, focusing on coagulation factors and adhesion molecules.
- In vivo studies involving neutrophil depletion and genetic reduction of migrasomes.
- Assessment of platelet plug formation and coagulation in vivo.
- Rescue experiments using purified neutrophil-derived migrasomes.
Main Results:
- Neutrophil-derived migrasomes are abundant in circulating blood.
- Migrasomes adsorb and enrich coagulation factors and adhesion molecules on their surface.
- Migrasomes accumulate at sites of vascular injury, promoting platelet activation and clot formation.
- Depletion of neutrophils or reduction of migrasomes impairs haemostasis.
- Administration of purified migrasomes rescues defective coagulation.
Conclusions:
- Neutrophil-derived migrasomes are essential, previously unrecognized components of the haemostasis system.
- These migrasomes actively participate in initiating and stabilizing blood clots.
- Understanding migrasome function may reveal causes of coagulation disorders and suggest new therapeutic strategies.
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