Endothelial cells proactively form microvilli-like membrane projections upon intercellular adhesion molecule 1

Christopher V Carman1, Chang-Duk Jun, Azucena Salas

  • 1Department of Pathology, CBR Institute for Biomedical Research, Inc., Harvard Medical School, Boston, MA 02115, USA.

Insights

Endothelial cells form ICAM-1-enriched cups around leukocytes upon LFA-1 binding. These structures, crucial for immune cell interaction, do not affect firm adhesion but may aid transendothelial migration.

Area of Science:

  • Cellular biology
  • Immunology
  • Biophysics

Background:

  • Leukocyte-endothelial interactions are vital for immunity and inflammation.
  • The molecular mechanisms governing these interactions are not fully understood.
  • Adhesion molecules like ICAM-1 and LFA-1 play key roles.

Purpose of the Study:

  • To investigate the dynamic distribution of ICAM-1 and LFA-1 during leukocyte-endothelial cell interactions.
  • To elucidate the structural and signaling pathways involved in these dynamic changes.
  • To determine the role of these structures in firm adhesion and potential transendothelial migration.

Main Methods:

  • Confocal microscopy was used to visualize ICAM-1 and LFA-1 dynamics.
  • Experiments involved activated human umbilical vein endothelial cells (HUVECs) and various LFA-1-bearing cells.
  • Inhibitors of cytoskeletal components and intracellular calcium were employed.

Main Results:

  • ICAM-1 rapidly relocalized to microvilli-like projections upon LFA-1 engagement, forming cup-like structures around leukocytes.
  • These projections clustered LFA-1 into linear tracks and were enriched in actin.
  • Projection formation was independent of VCAM-1/VLA-4, shear, Rho/ROCK signaling, but required intracellular calcium and intact cytoskeletons.
  • Disrupting these structures did not affect firm adhesion.

Conclusions:

  • The endothelium proactively forms ICAM-1-enriched cup-like structures in response to LFA-1 engagement.
  • These structures are not essential for firm leukocyte adhesion.
  • The findings suggest a potential role for these structures in leukocyte transendothelial migration.

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