Role of Glycocalyx in Flow-Induced Production of Nitric Oxide and Reactive Oxygen Species

Abstract

Although the glycocalyx has been implicated in wall shear stress (WSS) mechanotransduction, the role of glycocalyx components in nitric oxide (NO*) and reactive oxygen species (ROS) production remains unclear. Here, we tested the hypothesis that glycocalyx is implicated in both endothelial NO* and O2- production. Specifically, we evaluated the role of hyaluronic acid (HA), heparan sulfate (HS), and sialic acid (SA) in NO* and O2- mechanotransduction. Twenty-seven ex-vivo porcine superficial femoral arteries were incubated with either heparinase III, hyaluronidase, or neuraminidase, to remove HS, HA, or SA, respectively, from the glycocalyx. The arteries were then subjected to steady state flow and the effluent solution was measured for nitrites and the vessel diameter was tracked to quantify the degree of vasodilation. Our results show that removal of HA decreased both nitrites and vasodilation, and tempol treatment had no reversing effect. Degradation of HS proteoglycans decreased NO* bioavailability through an increase in O2- production as indicated by fluorescent signals of dihydroethidium (DHE) and its area fraction (209±24% increase) and also removed extracellular O2- dismutase (ecSOD) (67±9% decrease). The removal of SA also increased O2- production as indicated by DHE fluorescent signals (86±17% increase) and the addition of tempol, a mimic O2- scavenger, restored both NO* availability and vasodilation in both heparinase and neuraminidase treated vessels. This implies that HS and SA are not directly involved in WSS mediated NO* production. This study implicates HA in WSS-mediated NO* mechanotransduction and underscores the role of HS and SA in ROS regulation in vessel wall in response to WSS stimulation.