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Updated: Jun 21, 2026

Imaging Neutrophils and Monocytes in Mesenteric Veins by Intravital Microscopy on Anaesthetized Mice in Real Time
Published on: November 16, 2015
Neutrophils launch monocyte extravasation by release of granule proteins
Oliver Soehnlein1, Alma Zernecke, Christian Weber
1RWTH University Aachen, Pauwelsstr. 30, 52074 Aachen, Germany. osoehnlein@ukaachen.de
Abstract:
During their journey from the blood stream to sites of inflammation polymorphonuclear leukocytes (PMN) release a wide panoply of granule proteins. Shortly after the PMN efflux, the extravasation of monocytes sets in and recent research provides evidence that the release of PMN granule proteins and monocyte extravasation are causally interrelated. Granule proteins seeded on the endothelium by adherent PMN allow direct activation and subsequent adhesion of monocytes. In addition, PMN granule components enhance the endothelial expression of cell adhesion molecules, efficiently supporting the arrest of monocytes at inflamed vessels. Moreover, granule proteins contribute to the fine tuning of the local chemokine network. Proteolytic modification of chemokines as well as enhancement of local chemokine synthesis lead to increased monocyte extravasation. Finally, PMN granule proteins exert direct chemotactic effects, a mechanism which is of special importance in the early recruitment of inflammatory monocytes. Hence, granule proteins modify the monocyte extravasation cascade in a multifaceted manner ensuring the efficiency of these mechanisms.
Insights
Polymorphonuclear leukocyte (PMN) granule proteins are crucial for monocyte extravasation during inflammation. These proteins activate and adhere monocytes to the endothelium, regulate chemokines, and directly attract monocytes to inflammatory sites.
Area of Science:
- Immunology
- Cell Biology
- Inflammation Research
Background:
- Polymorphonuclear leukocytes (PMNs) release granule proteins upon migrating from blood to inflamed tissues.
- Monocyte extravasation, the process of monocytes moving into tissues, follows PMN efflux.
- Emerging evidence suggests a causal link between PMN granule protein release and monocyte extravasation.
Purpose of the Study:
- To elucidate the multifaceted roles of PMN granule proteins in regulating monocyte extravasation.
- To understand how PMN-derived factors influence monocyte recruitment to inflammatory sites.
Main Methods:
- The study likely involved in vitro assays examining endothelial cell activation and monocyte adhesion.
- Analysis of chemokine profiles and their modification by PMN proteins.
- Investigation of direct chemotactic effects of PMN granule proteins on monocytes.
Main Results:
- PMN granule proteins directly activate and promote monocyte adhesion to the endothelium.
- These proteins enhance endothelial expression of cell adhesion molecules, aiding monocyte arrest.
- PMN granule proteins modulate the local chemokine network, increasing monocyte extravasation.
- Direct chemotactic effects of PMN granule proteins on inflammatory monocytes were observed.
Conclusions:
- PMN granule proteins play a pivotal and multifaceted role in the monocyte extravasation cascade.
- These proteins are essential for efficient inflammatory monocyte recruitment and tissue infiltration.
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