Three-dimensional(3D)bioprinting,an effective technique for building cell-laden structures providing native extracellular matrix environments,presents challenges,including inadequate cellular interactions.To address t...Three-dimensional(3D)bioprinting,an effective technique for building cell-laden structures providing native extracellular matrix environments,presents challenges,including inadequate cellular interactions.To address these issues,cell spheroids offer a promising solution for improving their biological functions.Particularly,minispheroids with 50-100μm diameters exhibit enhanced cellular maturation.We propose a one-step minispheroid-forming bioprinting process incorporating electrical stimulation(E-MS-printing).By stimulating the cells,minispheroids with controlled diameters were generated by manipulating the bioink viscosity and stimulation intensity.To validate its feasibility,E-MS-printing process was applied to fabricate an engineered liver model designed to mimic the hepatic lobule unit.E-MS-printing was employed to print the hepatocyte region,followed by bioprinting the central vein using a core-shell nozzle.The resulting constructs displayed native liver-mimetic structures containing minispheroids,which facilitated improved hepatic cell maturation,functional attributes,and vessel formation.Our results demonstrate a new potential 3D liver model that can replicate native liver tissues.展开更多
基金supported by a grant from the Ministry of Trade,Industry&Energy(MOTIE,Korea)under Industrial Technology Innovation Program(20009652:Technology on commercialization and materials of Bioabsorbable Hydroxyapatite less than 1μm in size)supported by the“Korea National Institute of Health”research project(2022ER130501).
文摘Three-dimensional(3D)bioprinting,an effective technique for building cell-laden structures providing native extracellular matrix environments,presents challenges,including inadequate cellular interactions.To address these issues,cell spheroids offer a promising solution for improving their biological functions.Particularly,minispheroids with 50-100μm diameters exhibit enhanced cellular maturation.We propose a one-step minispheroid-forming bioprinting process incorporating electrical stimulation(E-MS-printing).By stimulating the cells,minispheroids with controlled diameters were generated by manipulating the bioink viscosity and stimulation intensity.To validate its feasibility,E-MS-printing process was applied to fabricate an engineered liver model designed to mimic the hepatic lobule unit.E-MS-printing was employed to print the hepatocyte region,followed by bioprinting the central vein using a core-shell nozzle.The resulting constructs displayed native liver-mimetic structures containing minispheroids,which facilitated improved hepatic cell maturation,functional attributes,and vessel formation.Our results demonstrate a new potential 3D liver model that can replicate native liver tissues.