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PMID: 14634129 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Endothelial cells proactively form microvilli-like membrane projections upon intercellular adhesion molecule 1 engagement of leukocyte LFA-1.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 171 ·No. 11 ·2003-12-01 ·Pages 6135-44

Carman CV, Jun CD, Salas A, Springer TA

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.

MeSH Terms
Actin Cytoskeleton/physiology Actins/metabolism Animals CHO Cells Calcium Signaling/physiology Cell Adhesion/physiology Cell Aggregation/physiology Cell Communication/physiology Cell Line Cell Membrane/metabolism,physiology Cell Movement/physiology Cells, Cultured Cricetinae Endothelium, Vascular/cytology,metabolism,physiology Humans Intercellular Adhesion Molecule-1/metabolism,physiology Intracellular Signaling Peptides and Proteins K562 Cells Leukocytes/cytology,metabolism,physiology Lymphocyte Function-Associated Antigen-1/metabolism,physiology Microscopy, Confocal Microtubules/physiology Microvilli/metabolism,physiology Protein Binding/physiology Protein Serine-Threonine Kinases/metabolism Stress, Mechanical rho-Associated Kinases
Chemicals
Actins Intracellular Signaling Peptides and Proteins Lymphocyte Function-Associated Antigen-1 Intercellular Adhesion Molecule-1 Protein Serine-Threonine Kinases rho-Associated Kinases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Carman Christopher V
Department of Pathology, CBR Institute for Biomedical Research, Inc., Harvard Medical School, Boston, MA 02115, USA.
Jun Chang-Duk
Salas Azucena
Springer Timothy A
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
2003-12-01
Pages
6135-44
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NCI NIH HHS · CA31798 · United States
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