Protein tyrosine kinases in neutrophil activation and recruitment

Arch Biochem Biophys. 2011 Jun 15;510(2):112-9. doi: 10.1016/j.abb.2011.02.009. Epub 2011 Feb 19.

Abstract

Migration of leukocytes into tissue is a key element of innate and adaptive immunity. The first contact of leukocytes with endothelial cells is mediated by engagement of selectins with their counter-receptors which results in leukocyte rolling. During rolling, leukocytes collect different inflammatory signals that activate intracellular signaling pathways. Integration of these signals induces leukocyte activation, firm arrest, post-adhesion strengthening, intravascular crawling, and transmigration. In neutrophils, like in T-cells and platelets, both G-protein-coupled receptor-dependent and -independent activation pathways exist that lead to integrin activation. Accumulating evidence suggests that different protein tyrosine kinases play key roles in signal transduction pathways regulating neutrophil activation and recruitment to inflammatory sites. This review focuses on the role of protein tyrosine kinases of the Src, Syk, and Tec families for neutrophil activation and recruitment.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Humans
  • Neutrophil Activation*
  • Neutrophil Infiltration*
  • Neutrophils / cytology
  • Neutrophils / enzymology
  • Neutrophils / immunology
  • Protein-Tyrosine Kinases / metabolism*
  • Signal Transduction

Substances

  • Protein-Tyrosine Kinases