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Published on: June 13, 2014
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.
Abstract:
Specific leukocyte/endothelial interactions are critical for immunity and inflammation, yet the molecular details of this interaction interface remain poorly understood. Thus, we investigated, with confocal microscopy, the distribution dynamics of the central adhesion molecules ICAM-1 and LFA-1 in this context. Monolayers of activated HUVECs stained with fluorescent anti-ICAM-1 Fabs or Chinese hamster ovary-K1 cells expressing ICAM-1-green fluorescent protein were allowed to bind LFA-1-bearing monocytes, neutrophils, or K562 LFA-1 transfectants. ICAM-1 was rapidly relocalized to newly formed microvilli-like membrane projections in response to binding LFA-1 on leukocytes. These ICAM-1-enriched projections encircled the leukocytes extending up their sides and clustered LFA-1 underneath into linear tracks. Projections formed independently of VCAM-1/very late Ag 4 interactions, shear, and proactive contributions from the LFA-1-bearing cells. In the ICAM-1-bearing endothelial cells, projections were enriched in actin but not microtubules, required intracellular calcium, and intact microfilament and microtubule cytoskeletons and were independent of Rho/Rho kinase signaling. Disruption of these projections with cytochalasin D, colchicine, or BAPTA-AM had no affect on firm adhesion. These data show that in response to LFA-1 engagement the endothelium proactively forms an ICAM-1-enriched cup-like structure that surrounds adherent leukocytes but is not important for firm adhesion. This finding leaves open a possible role in leukocyte transendothelial migration, which would be consistent with the geometry and kinetics of formation of the cup-like structure.
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