Signals regulating L-selectin-dependent leucocyte adhesion and transmigration

Int J Biochem Cell Biol. 2013 Mar;45(3):550-5. doi: 10.1016/j.biocel.2012.12.023. Epub 2013 Jan 5.

Abstract

L-selectin is a type I transmembrane cell adhesion molecule that is expressed on the surface of most circulating leukocytes. Studies in L-selectin knockout mice reveal a prominent role for this glycoprotein in health and disease, regulating leucocyte recruitment to peripheral lymph nodes (e.g. naïve T-cells) and sites of acute and chronic inflammation (e.g. monocytes and neutrophils). Clinical trials have revealed L-selectin as a promising target in some acute and chronic inflammatory diseases. Unearthing the intracellular signals that act directly downstream of L-selectin may also expose novel therapeutic targets in a cell type/disease-specific manner. This review will focus on L-selectin-dependent signalling - exploring the different signals that potentially arise from distinct phases of the multi-step adhesion cascade and the contribution of known binding partners of L-selectin in this response.

Publication types

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

MeSH terms

  • Animals
  • Calmodulin / genetics
  • Calmodulin / metabolism*
  • Cell Adhesion / genetics*
  • Cell Movement / genetics
  • Humans
  • Inflammation / metabolism*
  • L-Selectin / genetics
  • L-Selectin / metabolism*
  • Leukocytes* / cytology
  • Leukocytes* / metabolism
  • Mice
  • Protein Kinase C / metabolism
  • Signal Transduction

Substances

  • Calmodulin
  • L-Selectin
  • Protein Kinase C