Shear stress affects migration behavior of polymorphonuclear cells arrested on endothelium

Cell Immunol. 2000 Jul 10;203(1):39-46. doi: 10.1006/cimm.2000.1671.

Abstract

Polymorphonuclear cell (PMN) transmigration across the TNF-alpha-stimulated endothelial cell (HUVEC) monolayer in the presence of shear flow was monitored with time-lapse videotapes. More than half of the PMN that arrested on HUVEC transmigrated through endothelial cell junctions within the following 15 min. The kinetics of transmigration was significantly faster than that of PMN placed under static conditions. Once PMN crept into the subendothelial space, they showed random migration beneath the HUVEC monolayer. PMN that did not transmigrate moved on the apical surface of HUVEC in the direction of flow downstream. Anti-beta1 integrin mAb (4B4) and RGD peptide inhibited the transmigration more effectively than anti-beta2 integrin mAb (TS1/18) and almost totally abrogated transmigration. When HUVEC were cultured on fibronectin or laminin, the transmigration was significantly inhibited by anti-alpha5 or alpha6 integrin mAbs, respectively. Our data clearly indicate that shear stress affects the migration behavior of PMN arrested on endothelium and suggest that binding to subendothelial extracellular matrix via beta1 integrins is another essential step in leukocyte extravasation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / metabolism
  • Biomechanical Phenomena
  • CD18 Antigens / metabolism
  • Cell Movement*
  • Cells, Cultured
  • Chemotaxis, Leukocyte
  • Coculture Techniques
  • Endothelium, Vascular / cytology*
  • Endothelium, Vascular / drug effects
  • Hemodynamics
  • Humans
  • Integrin alpha5
  • Integrin alpha6
  • Integrin beta1 / metabolism
  • Integrins / metabolism*
  • Neutrophils / cytology*
  • Stress, Physiological*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Antigens, CD
  • CD18 Antigens
  • Integrin alpha5
  • Integrin alpha6
  • Integrin beta1
  • Integrins
  • Tumor Necrosis Factor-alpha