Key result
Stiff gelatin/CBMA hydrogel tubes exhibited higher velocity magnitude and wall shear stress, leading to lower endothelial cell vascular functions compared to soft tubes.
A novel in vitro vascular model using tunable hydrogel tubes demonstrates that increased vascular stiffness impairs endothelial function and increases sensitivity to injury.
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Endothelial stiffness sensitivity in tunable models extends in vitro vascular research; leaves open clinical translation pending in vivo validation.
Stiffness of blood vessels is one of the most important parameters involving in vascular diseases. However, no vascular model well mimics the stiffness of native blood vessels, and thus, the effects of vascular stiffness on endothelial cells cannot be studied in vitro. For this purpose, we fabricated the gelatin/carboxybetaine (CBMA) interpenetrating network (IPN) hydrogel tubes to exactly present the stiffness of soft (i.e., physical) and stiff (i.e., pathological) arteries in human. The vascular models are then constructed via endothelial cell culture inside the gel tubes under a cardiac-like pulsatile perfusion. As found, the velocity magnitude and wall shear stress in the stiff gel tube are much higher than those in the soft one. Correspondingly, the endothelial cells in the soft gel tube (i.e., physical model) express higher vascular functions than those in the stiff one (i.e., pathological model). Moreover, a pathological model was more sensitive to ethanol-induced vascular injury than the physical model. Thus, the new vascular models with a tunable stiffness provide a useful tool to investigate the stiffness involved mechanism in vascular diseases under in vivo mimicked microenvironments.
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Meng et al. (2018) studied Vascular diseases. Stiff gelatin/carboxybetaine (CBMA) interpenetrating network hydrogel tubes vs. Soft gelatin/CBMA hydrogel tubes was evaluated on Velocity magnitude, wall shear stress, and endothelial cell vascular functions. Stiff gelatin/CBMA hydrogel tubes exhibited higher velocity magnitude and wall shear stress, leading to lower endothelial cell vascular functions compared to soft tubes.
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