ESAM supports neutrophil extravasation, activation of Rho, and VEGF-induced vascular permeability

J Exp Med. 2006 Jul 10;203(7):1671-7. doi: 10.1084/jem.20060565. Epub 2006 Jul 3.

Abstract

Endothelial cell-selective adhesion molecule (ESAM) is specifically expressed at endothelial tight junctions and on platelets. To test whether ESAM is involved in leukocyte extravasation, we have generated mice carrying a disrupted ESAM gene and analyzed them in three different inflammation models. We found that recruitment of lymphocytes into inflamed skin was unaffected by the gene disruption. However, the migration of neutrophils into chemically inflamed peritoneum was inhibited by 70% at 2 h after stimulation, recovering at later time points. Analyzing neutrophil extravasation directly by intravital microscopy in the cremaster muscle revealed that leukocyte extravasation was reduced (50%) in ESAM(-/-) mice without affecting leukocyte rolling and adhesion. Depletion of >98% of circulating platelets did not abolish the ESAM deficiency-related inhibitory effect on neutrophil extravasation, indicating that it is only ESAM at endothelial tight junctions that is relevant for the extravasation process. Knocking down ESAM expression in endothelial cells resulted in reduced levels of activated Rho, a GTPase implicated in the destabilization of tight junctions. Indeed, vascular permeability stimulated by vascular endothelial growth factor was reduced in ESAM(-/-) mice. Collectively, ESAM at endothelial tight junctions participates in the migration of neutrophils through the vessel wall, possibly by influencing endothelial cell contacts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Capillary Permeability / genetics
  • Capillary Permeability / immunology*
  • Cell Adhesion Molecules / deficiency
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / physiology*
  • Cell Communication / genetics
  • Cell Communication / immunology
  • Cell Movement / genetics
  • Cell Movement / immunology*
  • Enzyme Activation / genetics
  • Enzyme Activation / immunology
  • Female
  • Male
  • Mice
  • Mice, Knockout
  • Neutrophils / immunology
  • Neutrophils / pathology*
  • Vascular Endothelial Growth Factor A / physiology*
  • rho GTP-Binding Proteins / metabolism*

Substances

  • Cell Adhesion Molecules
  • Esam protein, mouse
  • Vascular Endothelial Growth Factor A
  • vascular endothelial growth factor A, mouse
  • rho GTP-Binding Proteins