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1 Department of Chemical Engineering, The Pennsylvania State University, University Park, PA, USA
2 Department of Chemical Engineering, The Pennsylvania State University, University Park, PA, USA; Deparment of Biomedical Engineering, The City College of New York / CUNY, New York, NY, USA
3 Department of Anesthesiology, The University of Utah, Salt Lake City, UT, USA
4 Deparment of Biomedical Engineering, The City College of New York / CUNY, New York, NY, USA
* To whom correspondence should be addressed. E-mail: kma169{at}psu.edu.
This study addressed the influence of the rate of shear stress application on aortic smooth muscle cell contraction and the role of specific glycosaminoglycans in this mechanotransduction. Rat aortic smooth muscle cells (SMCs) were exposed to either a step increase in shear stress (0 to 25 dynes/cm2) or a ramp increase in shear stress (0 to 25 dynes/cm2 over 5 minutes) in a parallel plate flow chamber, and cell contraction was characterized by cell area reduction. SMCs contracted at levels similar to those reported previously and equally in response to both a step and ramp increase in shear stress. When the cells were pre-treated with heparinase III or chondroitinase ABC to remove glycosaminoglycans (GAGs), heparan sulfate and chondroitin sulfate, respectively, from the glycocalyx, the contraction response to increases in shear stress was significantly inhibited. These studies indicate that specific components of the SMC glycocalyx play an important role in the mechanotransduction of shear stress into a contractile response and that the rate of application of shear stress does not affect the SMC contraction.
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