Gas6 promotes inflammation by enhancing interactions between endothelial cells, platelets, and leukocytes

Blood. 2008 Apr 15;111(8):4096-105. doi: 10.1182/blood-2007-05-089565. Epub 2007 Dec 21.

Abstract

The role of Gas6 in endothelial cell (EC) function remains incompletely characterized. Here we report that Gas6 amplifies EC activation in response to inflammatory stimuli in vitro. In vivo, Gas6 promotes and accelerates the sequestration of circulating platelets and leukocytes on activated endothelium as well as the formation and endothelial sequestration of circulating platelet-leukocyte conjugates. In addition, Gas6 promotes leukocyte extravasation, inflammation, and thrombosis in mouse models of inflammation (endotoxinemia, vasculitis, heart transplantation). Thus, Gas6 amplifies EC activation, thereby playing a key role in enhancing the interactions between ECs, platelets, and leukocytes during inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axl Receptor Tyrosine Kinase
  • Blood Platelets / metabolism
  • Blood Platelets / pathology*
  • Cell Communication*
  • Cell Line
  • Endothelial Cells / enzymology
  • Endothelial Cells / pathology*
  • Endothelium / metabolism
  • Heart Transplantation
  • Humans
  • Inflammation / metabolism*
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Leukocytes / metabolism
  • Leukocytes / pathology*
  • Mice
  • Mice, Inbred C57BL
  • Myocardial Ischemia / metabolism
  • Myocardial Ischemia / pathology
  • Oncogene Proteins / metabolism
  • P-Selectin / metabolism
  • Proto-Oncogene Proteins
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Vasculitis / metabolism
  • Vasculitis / pathology

Substances

  • Intercellular Signaling Peptides and Proteins
  • Oncogene Proteins
  • P-Selectin
  • Proto-Oncogene Proteins
  • growth arrest-specific protein 6
  • Receptor Protein-Tyrosine Kinases
  • Axl Receptor Tyrosine Kinase