Facile Engineering of Long‐Term Culturable Ex Vivo Vascularized Tissues Using Biologically Derived Matrices
Year: 2018
Type: article
Abstract: Recent advances in tissue engineering and 3D bioprinting have enabled construction of cell-laden scaffolds containing perfusable vascular networks. Although these methods partially address the nutrient-diffusion limitations present in engineered tissues, they are still restricted in both their viable vascular geometries and matrix material compatibility. To address this, tissue constructs are engineered via encapsulation of 3D printed, evacuable, free standing scaffolds of poly(vinyl alcohol) (PVA) in biologically derived matrices. The ease of printability and water-soluble nature of PVA grant compatibility with biologically relevant matrix materials and allow for easily repeatable generation of complex vascular patterns. This study confirms the ability of this approach to produce perfusable vascularized matrices capable of sustaining both cocultures of multiple cell types and excised tumor fragments ex vivo over multiple weeks. The study further demonstrates the ability of the approach to produce hybrid patterns allowing for coculture of vasculature and epithelial cell-lined lumens in close proximity, thereby enabling ex vivo recapitulation of gut-like systems. Taken together, the methodology is versatile, broadly applicable, and importantly, simple to use, enabling ready applicability in many research settings. It is believed that this technique has the potential to significantly accelerate progress in engineering and study of ex vivo organotypic tissue constructs.
Source: Advanced Healthcare Materials
Institution: University of California San Diego
Language: English
Subfield: Biomedical Engineering
Field: Engineering
Domain: Physical Sciences
Open Access status: green
Funders: National Science Foundation, Burroughs Wellcome Fund, March of Dimes Foundation, Sidney Kimmel Foundation, National Institutes of Health, University of California, San Diego, National Heart, Lung, and Blood Institute, National Human Genome Research Institute, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke
Awards: G1405814600, G1638026032, G1928110987, Systematic mapping of genetic vulnerabilities in head and neck cancer, Biomaterial Mimicry of Dynamic Matrix Stiffening During Tumor Progression, Developing Adhesome Technology as a Physical Marker of Highly Metastatic Cells, University of California San Diego Neuroscience Microscopy Imaging Core, Strain-Activated Signaling within Cell Adhesions Dictates Cell Fate, Dissecting the interplay of gene regulatory networks and cellular niche on cell fate determination, Next-generation Functional Genetic Screening of Un-screenable Traits, Integrative Bioengineering of Heart, Vessels, and Blood
OpenAlex ID: W2898170191
