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VASCULAR BIOLOGY
Departments of 1Genomics and Pathobiology and 3Pathology, University of Alabama at Birmingham, Birmingham, Alabama 35294; 2Department of Pathology, Louisiana State University Health Sciences Center, Shreveport, Louisiana 71130; and4 Research Service, Birmingham Department of Veterans Affairs Medical Center, Birmingham, Alabama 35233
Submitted 18 July 2002 ; accepted in final form 3 March 2003
Leukocyte rolling, adhesion, and migration on vascular endothelium involve
several sets of adhesion molecules that interact simultaneously. Each of these
receptor-ligand pairs may play multiple roles. We examined the role of ICAM-1
in adhesive interactions with mouse aortic endothelial cells (MAECs) in an in
vitro flow system. Average rolling velocity of the monocytic cell line WEHI
274.1 was increased on ICAM-1-deficient MAECs compared with wild-type MAECs,
both with and without TNF-
stimulation. High-temporal-resolution
analysis provided insights into the underlying basis for these differences.
Without TNF-
stimulation, average rolling velocity was slower on
wild-type than on ICAM-1-deficient endothelium because of brief (<1 s)
pauses. On TNF-
-stimulated ICAM-1-deficient endothelium, cells rolled
faster because of transient accelerations, producing "jerky"
rolling. Firm adhesion to ICAM-1-deficient MAECs was significantly reduced
compared with wild-type MAECs, although the number of rolling cells was
similar. These results demonstrate directly that ICAM-1 affects rolling
velocity by stabilizing leukocyte rolling.
intercellular adhesion molecule-1; cell adhesion; leukocytes; vascular endothelium; videomicroscopy
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