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Regulation of Leukocyte Recruitment on Inflamed Endothelium
Sponsored by the Biomedical Engineering Society
Mon. April 3 — 3:15-5:15 PM
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| Chaired: |
Scott I. Simon, Univ. of California, Davis |
Discovery of new genes and proteins directly supporting leukocyte adhesion
is waning, whereas there is heightened interest in the cell mechanics and
receptor dynamics that lead from transient tethering via selectins to
affinity shifts and adhesion strengthening through integrins. New optical
tools enable real-time imaging of leukocyte rolling and arrest in parallel
plate flow channels (PPFCs), and detection of single-molecule force
spectroscopy provides an inner view of the intercellular adhesive contact
region. Leukocyte recruitment during acute inflammation is triggered by
ligation of G protein-coupled chemotactic receptors (GPCRs) and clustering
of selectins. This, in turn, activates β2-integrin (CD18),
which facilitates cell capture and arrest in shear flow. This symposium
will focus on the molecular events linking selectins, integrins and GPCRs
in leukocyte recruitment.
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3:15 PM |
Dynamic
shifts in LFA-1 affinity regulate neutrophil rolling, arrest, and
transmigration on inflamed endothelium.
Scott Simon, Univ. of California, Davis
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3:35 PM |
Deficiency of Wiskott-Aldrich Syndrome protein results in impaired
integrin-mediated neutrophil arrest and transmigration.
Clifford Lowell, UCSF
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4:00 PM |
Characterization of E-selectin ligands on neutrophils.
Paul Frenette, Mt. Sinai Sch. of Med.
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4:25 PM |
Role of
PI3kinase gamma in neutrophil arrest under flow.
Klaus Ley, Univ. of Virginia
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4:50 PM |
Adhesion-induced Mechanotransduction: a novel mechanism for
endothelial cell activation.
Kamala Patel, Univ. of Calgary
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