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Rapid casting of patterned vascular networks for perfusable engineered 3D tissues

In the absence of perfusable vascular networks, three-dimensional (3D) engineered tissues densely populated with cells quickly develop a necrotic core [1]. Yet the lack of a general approach to rapidly construct such networks remains a major challenge for 3D tissue culture [2–4]. Here, we 3D printed...

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Detalles Bibliográficos
Autores principales: Miller, Jordan S., Stevens, Kelly R., Yang, Michael T., Baker, Brendon M., Nguyen, Duc-Huy T., Cohen, Daniel M., Toro, Esteban, Chen, Alice A., Galie, Peter A., Yu, Xiang, Chaturvedi, Ritika, Bhatia, Sangeeta N., Chen, Christopher S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586565/
https://www.ncbi.nlm.nih.gov/pubmed/22751181
http://dx.doi.org/10.1038/nmat3357
Descripción
Sumario:In the absence of perfusable vascular networks, three-dimensional (3D) engineered tissues densely populated with cells quickly develop a necrotic core [1]. Yet the lack of a general approach to rapidly construct such networks remains a major challenge for 3D tissue culture [2–4]. Here, we 3D printed rigid filament networks of carbohydrate glass, and used them as a cytocompatible sacrificial template in engineered tissues containing living cells to generate cylindrical networks which could be lined with endothelial cells and perfused with blood under high-pressure pulsatile flow. Because this simple vascular casting approach allows independent control of network geometry, endothelialization, and extravascular tissue, it is compatible with a wide variety of cell types, synthetic and natural extracellular matrices (ECMs), and crosslinking strategies. We also demonstrated that the perfused vascular channels sustained the metabolic function of primary rat hepatocytes in engineered tissue constructs that otherwise exhibited suppressed function in their core.