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Transport-mediated angiogenesis in 3D epithelial coculture

Authors
Sudo, R.Chung, S.Zervantonakis, I.K.Vickerman, V.Toshimitsu, Y.Griffith, L.G.Kamm, R.D.
Issue Date
2009
Keywords
Microfluidics; Tissue engineering; Vascularization
Citation
FASEB Journal, v.23, no.7, pp.2155 - 2164
Indexed
SCOPUS
Journal Title
FASEB Journal
Volume
23
Number
7
Start Page
2155
End Page
2164
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/121855
DOI
10.1096/fj.08-122820
ISSN
0892-6638
Abstract
Increasing interest has focused on capturing the complexity of tissues and organs in vitro as models of human pathophysiological processes. In particular, a need exists for a model that can investigate the interactions in three dimensions (3D) between epithelial tissues and a microvascular network since vascularization is vital for reconstructing functional tissues in vitro. Here, we implement a microfluidic platform to analyze angiogenesis in 3D cultures of rat primary hepatocytes and rat/human microvascular endothelial cells (rMVECs/hMVECs). Liver and vascular cells were cultured on each sidewall of a collagen gel scaffold between two microfluidic channels under static or flow conditions. Morphogenesis of 3D hepatocyte cultures was found to depend on diffusion and convection across the nascent tissue. Furthermore, rMVECs formed 3D capillary-like structures that extended across an intervening gel to the hepatocyte tissues in hepatocyter-MVEC coculture while they formed 2D sheet-like structures in rMVEC monoculture. In addition, diffusion of fluorescent dextran across the gel scaffold was analyzed, demonstrating that secreted proteins from the hepatocytes and MVECs can be exchanged across the gel scaffold by diffusional transport. The experimental approach described here is useful more generally for investigating microvascular networks within 3D engineered tissues with multiple cell types in vitro. © FASEB.
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