Key result
Hydrostatic pressure and shear stress applied to endothelial cells decreased ET-1 production, whereas NO synthesis was up-regulated by shear stress but not modulated by hydrostatic pressure.
Hydrostatic pressure and shear stress exert distinct effects on endothelial cell function, with shear stress up-regulating NO synthesis while both forces decrease ET-1 production.
No change to clinical management indicated; leaves open in vivo translation of differential endothelial mechanotransduction.
Abundant experimental evidence demonstrates that endothelial cells are sensitive to flow; however, the effect of fluid pressure or pressure gradients that are used to drive viscous flow is not well understood. There are two principal physical forces exerted on the blood vessel wall by the passage of intra‐luminal blood: pressure and shear. To analyze the effects of pressure and shear independently, these two stresses were applied to cultured cells in two different types of bioreactors: a pressure‐controlled bioreactor and a laminar flow bioreactor, in which controlled levels of pressure or shear stress, respectively, can be generated. Using these bioreactor systems, endothelin‐1 (ET‐1) and nitric oxide (NO) release from human umbilical vein endothelial cells were measured under various shear stress and pressure conditions. Compared to the controls, a decrease of ET‐1 production by the cells cultured in both bioreactors was observed, whereas NO synthesis was up‐regulated in cells under shear stress, but was not modulated by hydrostatic pressure. These results show that the two hemodynamic forces acting on blood vessels affect endothelial cell function in different ways, and that both should be considered when planning in vitro experiments in the presence of flow. Understanding the individual and synergic effects of the two forces could provide important insights into physiological and pathological processes involved in vascular remodeling and adaptation.
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Vozzi et al. (2013) studied this question. Hydrostatic pressure and shear stress vs. Controls was evaluated on Endothelin-1 (ET-1) and nitric oxide (NO) release. Hydrostatic pressure and shear stress applied to endothelial cells decreased ET-1 production, whereas NO synthesis was up-regulated by shear stress but not modulated by hydrostatic pressure.
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