Leukocyte polarization in cell migration and immune interactions

EMBO J. 1999 Feb 1;18(3):501-11. doi: 10.1093/emboj/18.3.501.

Abstract

Cell migration plays a key role in a wide variety of biological phenomena. This process is particularly important for leukocyte function and the inflammatory response. Prior to migration leukocytes undergo polarization, with the formation of a lamellipodium at the leading edge and a uropod at the trailing edge. This cell shape allows them to convert cytoskeletal forces into net cell-body displacement. Leukocyte chemoattractants, including chemokines, provide directional cues for leukocyte motility, and concomitantly induce polarization. Chemoattractant receptors, integrins and other adhesion molecules, cytoskeletal proteins and intracellular regulatory molecules change their cellular localization during cell polarization. A complex system of signal transduction molecules, including tyrosine kinases, lipid kinases, second messengers and members of the Rho family of small GTPases is thought to regulate the cytoskeletal rearrangements underlying leukocyte polarization and migration. The elucidation of the mechanisms and signals that control this complex reorganization will lead to a better understanding of critical questions in cell biology of leukocyte migration and polarity.

Publication types

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

MeSH terms

  • Animals
  • Calcium / metabolism
  • Cell Communication
  • Cell Movement / immunology*
  • Cell Movement / physiology*
  • Cell Polarity / immunology*
  • Cell Polarity / physiology*
  • Chemokines / physiology
  • Cyclic AMP / metabolism
  • Cytoskeleton / physiology
  • GTP Phosphohydrolases / metabolism
  • Humans
  • Leukocytes / cytology
  • Leukocytes / immunology*
  • Leukocytes / physiology*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Protein Kinases / metabolism
  • Receptors, Cell Surface / metabolism
  • Signal Transduction

Substances

  • Chemokines
  • Receptors, Cell Surface
  • Cyclic AMP
  • Protein Kinases
  • Phosphatidylinositol 3-Kinases
  • GTP Phosphohydrolases
  • Calcium