Key result
Novel 3D-printed microfluidic stenosis model successfully replicates atherogenic shear stresses to study endothelial dysfunction.
Why the study?
Atherosclerosis involves complex interactions of disturbed hemodynamics, endothelial dysfunction, and inflammation that require in vitro modeling to study flow disturbances and vascular inflammation.
A novel 3D-printed microfluidic stenosis model successfully recapitulates atherogenic flow disturbances and vascular inflammation, offering a platform for testing cardiovascular drugs and risk stratification.
Blood vessel narrowing and arterial occlusion are pathological hallmarks of atherosclerosis, which involves a complex interplay of perturbed hemodynamics, endothelial dysfunction and inflammatory cascade. Herein, we report a novel circular microfluidic stenosis model that recapitulates atherogenic flow-mediated endothelial dysfunction and blood-endothelial cell (EC) interactions in vitro . 2D and 3D stenosis microchannels with different constriction geometries were fabricated using 3D printing to study flow disturbances under varying severity of occlusion and wall shear stresses (100 to 2000 dynecm −2 ). Experimental and fluid simulation results confirmed the presence of pathological shear stresses in the stenosis region, and recirculation flow post stenosis. The resultant pathological flow profile induced pro-inflammatory and pro-thrombotic EC state as demonstrated by orthogonal EC alignment, enhanced platelet adhesion at the stenosis, and aberrant leukocyte-EC interactions post stenosis. Clinical utility of the vascular model was further investigated by testing anti-thrombotic and immunomodulatory efficacy of aspirin and metformin, respectively. Overall, the platform enables multi-factorial analysis of critical atherogenic events including endothelial dysfunction, platelets and leukocyte adhesion, and can be further developed into a liquid biopsy tool for cardiovascular risk stratification.
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Menon et al. (2020) studied Atherosclerosis. 3D stenosis microfluidic model was evaluated on Atherogenic flow-mediated endothelial dysfunction and blood-endothelial cell interactions. A novel 3D printed microfluidic stenosis model successfully recapitulated atherogenic flow disturbances and pathological shear stresses (100 to 2000 dyne/cm2) to study endothelial dysfunction.
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