| Literature DB >> 26950595 |
Boyang Zhang1,2, Miles Montgomery1,2, M Dean Chamberlain2, Shinichiro Ogawa3, Anastasia Korolj1,2, Aric Pahnke1,2, Laura A Wells2, Stéphane Massé4, Jihye Kim5, Lewis Reis2, Abdul Momen6, Sara S Nunes2,6,7, Aaron R Wheeler2,5, Kumaraswamy Nanthakumar4, Gordon Keller3, Michael V Sefton1,2, Milica Radisic1,2,6,7.
Abstract
We report the fabrication of a scaffold (hereafter referred to as AngioChip) that supports the assembly of parenchymal cells on a mechanically tunable matrix surrounding a perfusable, branched, three-dimensional microchannel network coated with endothelial cells. The design of AngioChip decouples the material choices for the engineered vessel network and for cell seeding in the parenchyma, enabling extensive remodelling while maintaining an open-vessel lumen. The incorporation of nanopores and micro-holes in the vessel walls enhances permeability, and permits intercellular crosstalk and extravasation of monocytes and endothelial cells on biomolecular stimulation. We also show that vascularized hepatic tissues and cardiac tissues engineered by using AngioChips process clinically relevant drugs delivered through the vasculature, and that millimetre-thick cardiac tissues can be engineered in a scalable manner. Moreover, we demonstrate that AngioChip cardiac tissues implanted with direct surgical anastomosis to the femoral vessels of rat hindlimbs establish immediate blood perfusion.Entities:
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Year: 2016 PMID: 26950595 PMCID: PMC4879054 DOI: 10.1038/nmat4570
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 43.841