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Updated: Jun 11, 2026

Real-time Imaging of Endothelial Cell-cell Junctions During Neutrophil Transmigration Under Physiological Flow
Published on: August 14, 2014
Phosphorylation of leukocyte PECAM and its association with detergent-resistant membranes regulate transendothelial
Oliver Florey1, Joanne Durgan, William Muller
1Department of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA. floreyo@mskcc.org
Abstract:
Leukocyte migration across the endothelial lining is a critical step in the body's response to infection and inflammation. The homophilic interaction between endothelial PECAM and leukocyte PECAM is essential for this process. The molecular events that are triggered in the endothelial cell by PECAM engagement have been well characterized; however, the function of leukocyte PECAM remains to be elucidated. To study this, we first blocked leukocyte transmigration using anti-PECAM Ab and then specifically activated leukocyte PECAM. This was sufficient to overcome the block and promote transmigration, suggesting an active signaling role for leukocyte PECAM. Consistent with this, we found that ligation of leukocyte PECAM induces phosphorylation of two tyrosine residues on its cytoplasmic tail. By performing RNA interference-rescue experiments, we demonstrate that these phosphorylation events are indispensable for transendothelial migration. Finally, we show that leukocyte PECAM translocates to a detergent-resistant membrane (DRM) during transmigration. PECAM localized in DRMs displays reduced phosphorylation and does not support transmigration. Together, these data support a model whereby engagement of leukocyte PECAM induces its transient tyrosine phosphorylation and induction of downstream signals that drive transmigration. These signals are then downregulated following PECAM translocation to DRMs.
Insights
Leukocyte PECAM signaling is crucial for immune cell transmigration. Its transient tyrosine phosphorylation and downstream signaling drive cell movement, while translocation to detergent-resistant membranes downregulates these signals.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- Leukocyte migration is vital for immune responses.
- Endothelial PECAM and leukocyte PECAM interactions facilitate this process.
- The specific role of leukocyte PECAM signaling was unclear.
Purpose of the Study:
- To elucidate the signaling function of leukocyte PECAM during transendothelial migration.
- To identify key molecular events mediated by leukocyte PECAM.
Main Methods:
- Blocking leukocyte transmigration with anti-PECAM antibodies.
- Activating leukocyte PECAM to observe effects on migration.
- Analyzing tyrosine phosphorylation of leukocyte PECAM.
- Utilizing RNA interference-rescue experiments.
- Investigating leukocyte PECAM localization in detergent-resistant membranes (DRMs).
Main Results:
- Activation of leukocyte PECAM overcame transmigration blockade, indicating an active signaling role.
- Ligation of leukocyte PECAM induced tyrosine phosphorylation on its cytoplasmic tail.
- These phosphorylation events were essential for transendothelial migration.
- Leukocyte PECAM translocated to DRMs during migration, where phosphorylation decreased.
Conclusions:
- Leukocyte PECAM engagement triggers transient tyrosine phosphorylation and downstream signaling necessary for transendothelial migration.
- PECAM translocation to DRMs leads to signal downregulation, regulating the migration process.
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