In vitro angiogenesis assay for the study of cell-encapsulation therapyElectronic supplementary information (ESI) available. See DOI: 10.1039/c2lc40182g

Cell encapsulation within alginate beads has potential as a sustained release system for delivering therapeutic agents in vivo while protecting encapsulated cells from the immune system. There is, however, no in vitro model for cell-encapsulation therapy that provides a suitable platform for quantit...

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Bibliographic Details
Main Authors Kim, Choong, Chung, Seok, Yuchun, Liu, Kim, Min-Cheol, Chan, Jerry K. Y, Asada, H. Harry, Kamm, Roger D
Format Journal Article
LanguageEnglish
Published 17.07.2012
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Summary:Cell encapsulation within alginate beads has potential as a sustained release system for delivering therapeutic agents in vivo while protecting encapsulated cells from the immune system. There is, however, no in vitro model for cell-encapsulation therapy that provides a suitable platform for quantitative assessment of physiological responses to secreted factors. Here we introduce a new microfluidic system specifically designed to evaluate and quantify the pro -angiogenic potential of factors secreted from human fetal lung fibroblasts encapsulated in beads on an intact endothelial cell monolayer. We confirmed that cell-encapsulating beads induced an angiogenic response in vitro , demonstrated by a strong correlation between the encapsulated cell density in the beads and the length of the vascular lumen formed in vitro . Conditions established by in vitro tests were then further shown to exert a pro -angiogenic response in vivo using a subcutaneous mouse model, forming an extensive network of functional luminal structures perfused with red blood cells. We introduce a new assay for evaluating and quantifying capillary growth from an intact endothelial cell monolayer in response to factors released from human fetal lung fibroblasts encapsulated in beads.
Bibliography:10.1039/c2lc40182g
Electronic supplementary information (ESI) available. See DOI
ISSN:1473-0197
1473-0189
DOI:10.1039/c2lc40182g