Fluid shear stress increases the intra-cellular storage pool of tissue-type plasminogen activator in intact human conduit vessels
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Updated: Oct 13, 2026

Electrophysiological Recordings of Single-cell Ion Currents Under Well-defined Shear Stress
Published on: August 2, 2019
L S Sjögren1, L Gan, R Doroudi
1Clinical Experimental Research Laboratory, Heart and Lung Insitute, Sahlgrenska University Hospital/Ostra, Göteborg University, Sweden.
Abstract:
We investigated the effect of shear stress on the expression of tissue-type plasminogen activator (t-PA) in intact human conduit vessels. Human umbilical veins were exposed to high or low shear stress (25 vs < 4 dyn/cm2) at identical intraluminal pressure (20 mmHg) for 1.5, 3, and 6 h in a new computerized biomechanical perfusion system. High shear perfusion induced a marked, time-dependent increase in t-PA immunostaining in both the endothelium and the media. t-PA relative to GAPDH gene expression increased by 54 +/- 14% in high- compared to low-sheared vessels (p = 0.002). By contrast, t-PA release into the perfusion medium was similar in vessels perfused under high or low shear stress conditions. The results show that shear stress independently of pressure is a potent fluid mechanical stimulus for up-regulation of the intracellular storage pool of t-PA in the vascular wall of fresh human conduit vessels. The shear effect is associated with an increased t-PA gene expression.
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