Elastic moduli of polyelectrolyte multilayer films regulate endothelium-blood interaction under dynamic conditions

A broad spectrum of biomaterials has been explored in order to design cardiovascular implants of sufficient hemocompatibility. Most of them were extensively tested for the ability to facilitate repopulation by patient cells. It was shown that stiffness, surface roughness, or hydrophilicity of polyelectrolyte films have an impact on adhesion, proliferation, and differentiation of cells. At the same time, it is still unknown how these properties influence cell functionality and as a consequence interactions with blood components under dynamic conditions. In this study, we aimed to determine the impact of chemical cross-linking of Chitosan (Chi) and Chrondroitin Sulphate (CS) on endothelium-blood cross-talk. We have found that the morphology of the endothelium monolayer was not altered by changes in coating properties. However, free radical generation by endothelial cells varied depending on the elastic properties of the coating. Simultaneously, we have observed a significant decrease in the level of adhering and circulating active platelets as well as aggregates when the endothelium monolayer was formed on stiffer films than on the other coating variants. Moreover, the same type of films has promoted significantly higher adhesion of blood morphotic elements when they were not functionalized by endothelium. The observed changes in hemocompatibility indicate the importance of a design of coatings that will promote cellularization in vivo in a relatively short time and which will regulate cell function.

Automated summary

The impact of chemical cross-linking of Chitosan and Chrondroitin Sulfate on the interaction between endothelial cells and blood was studied. The elasticity of the coating was found to significantly affect free radical generation by endothelial cells and platelet adhesion. Endothelium monolayers formed on stiffer films showed decreased adhesion and circulating active platelets, but promoted higher adhesion of blood morphotic elements. These observations highlight the importance of coating design in promoting cellularization and regulating cell function in vivo.