A central role for microvillous receptor presentation in leukocyte adhesion under flow

Cell. 1995 Sep 22;82(6):989-99. doi: 10.1016/0092-8674(95)90278-3.


Leukocyte adhesion to endothelium requires specialized mechanisms for contact initiation under flow. L-selectin (CD62L), an efficient initiator of adhesion, is clustered on the tips of leukocyte microvilli. To test whether microvillous presentation is critical for contact formation ("tethering"), we transfected lymphoid cells with chimeras of L-selectin and CD44, an adhesion molecule that is excluded from microvilli. CD44 transmembrane and intracellular (TM-IC) domains targeted the L-selectin ectodomain to the planar body, whereas L-selectin TM-IC segments conferred CD44 ectodomain clustering on microvilli. Wild-type and chimeric transfectants bound similarly to anti-ectodomain MAbs in static assays, but MAb binding under flow was much more efficient in the context of microvillous presentation. Similarly, wild-type and chimeric L-selectin possessed equivalent lectin activity, but microvillous presentation dramatically enhanced contact initiation on a native ligand. These findings demonstrate a critical role for receptor topography in leukocyte adhesion and suggest a novel regulatory mechanism of leukocyte trafficking.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • B-Lymphocytes / ultrastructure*
  • Cell Adhesion / immunology*
  • Endothelium / cytology
  • Humans
  • Hyaluronan Receptors / immunology
  • Hyaluronan Receptors / metabolism
  • L-Selectin / immunology
  • Lymphoma, B-Cell / pathology
  • Lymphoma, B-Cell / ultrastructure
  • Mice
  • Microscopy, Immunoelectron
  • Microvilli / immunology
  • Microvilli / ultrastructure*
  • Protein Binding / immunology
  • Recombinant Fusion Proteins / immunology
  • Rheology
  • Transfection / immunology
  • Tumor Cells, Cultured / immunology
  • Tumor Cells, Cultured / metabolism


  • Hyaluronan Receptors
  • Recombinant Fusion Proteins
  • L-Selectin