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Mechano-Sensing at the Vessel Wall in Regulation of
Atherogenesis
Sponsored by
The Biomedical Engineering Society
Cell Physiology Track
Tuesday, April 8 — 3:15 PM-5:15 PM
San Diego Convention Center — Room 27
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| Chaired: |
Scott I. Simon, Univ. of California,
Davis
Tzung K. Hsiai, Univ. of Southern California |
Endothelial cells transmit mechanical stimuli from
flowing blood into intracellular signaling through a process called
mechanotransduction. It is well established that fluid shear stress of
blood flow under laminar conditions in arteries is anti-inflammatory.
However, disturbed flow, including low and oscillatory shear that occur
under geometries of vessel bifurcation and bends in the wall promotes
oxidative stress and inflammatory responses with relevance to
atherogenesis. This symposium will present computational, optical and
molecular approaches to elucidate the role of shear force and
concomitant endothelial and adventitial cell stress and strain in
atherogenesis. The objective is to present a synopsis of the intricate
mechanosensing processes and signaling pathways employed by the
endothelium to transduce force into biological events affecting vascular
health and progression to disease.
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3:15 PM |
Shear
stress regulates mitochondria membrane potential via NO signaling.
Tzung Hsiai, Univ. of Southern California
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3:35 PM |
Spatial
regulation of adhesion molecule expression and monocyte recruitment
to human aortic endothelial cells under shear flow.
Michael Gower, Univ. of California, Davis
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3:55 PM |
Modulation of EC-SMC interaction by shear stress.
Shu Chien, UCSD
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4:15 PM |
Regulation of angiogenic responses by shear stress in endothelial
cells.
Hanjoong Jo, Georgia Tech/Emory Univ.
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4:35 PM |
Mitochondria, NO and endothelial mechanosignaling.
Rita Aleviradou, The Ohio State Univ.
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4:55 PM |
General discussion
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