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channels
1 Department of Human Physiology, School of Medicine, and 2 Department of Mechanical and Aeronautical Engineering, University of California, Davis, California 95616
Steady laminar
shear stress has been shown previously to markedly increase Na-K-Cl
cotransporter mRNA and protein in human umbilical vein endothelial
cells and also to rapidly increase endothelial K+ and
Cl
channel conductances. The present study was done to
evaluate the effects of shear stress on Na-K-Cl cotransporter activity and protein expression in bovine aortic endothelial cells (BAEC) and to
determine whether changes in cotransporter expression may be dependent
on early changes in K+ and Cl
channel
conductances. Confluent BAEC monolayers were exposed in a
parallel-plate flow chamber to either steady shear stress (19 dyn/cm2) or purely oscillatory shear stress (0 ± 19 dyn/cm2) for 6-48 h. After shearing, BAEC monolayers
were assessed for Na-K-Cl cotransporter activity or were subjected to
Western blot analysis of cotransporter protein. Steady shear stress led
to a 2- to 4-fold increase in BAEC cotransporter protein levels and a
1.5- to 1.8-fold increase in cotransporter activity, increases that
were sustained over the longest time periods studied. Oscillatory flow,
in contrast, had no effect on cotransporter protein levels. In the
presence of flow-sensitive K+ and Cl
channel
pharmacological blockers, the steady shear stress-induced increase in
cotransporter protein was virtually abolished. These results suggest
that shear stress modulates the expression of the BAEC Na-K-Cl
cotransporter by mechanisms that are dependent on flow-activated ion channels.
endothelium; mechanotransduction; ion channels
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