Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0050582
Title: Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting
Authors: Chan J.M. 
Zervantonakis I.K.
Rimchala T.
Polacheck W.J.
Whisler J.
Kamm R.D.
Keywords: alginic acid
collagen type 1
angiogenesis
article
capillary
cell viability
coculture
controlled study
encapsulation
fibroblast
gel
genetic transfection
human
human cell
immunocytochemistry
in vitro study
microfluidics
perfusion
plasmid
self directed angiogenic sprouting
tissue engineering
Alginates
Capillaries
Cells, Cultured
Coculture Techniques
Glucuronic Acid
Hexuronic Acids
Humans
Immunohistochemistry
Microfluidics
Neovascularization, Physiologic
Tissue Scaffolds
Issue Date: 2012
Citation: Chan J.M., Zervantonakis I.K., Rimchala T., Polacheck W.J., Whisler J., Kamm R.D. (2012). Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting. PLoS ONE 7 (12) : e50582. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0050582
Rights: Attribution 4.0 International
Abstract: In recent years, microfluidic systems have been used to study fundamental aspects of angiogenesis through the patterning of single-layered, linear or geometric vascular channels. In vivo, however, capillaries exist in complex, three-dimensional (3D) networks, and angiogenic sprouting occurs with a degree of unpredictability in all x,y,z planes. The ability to generate capillary beds in vitro that can support thick, biological tissues remains a key challenge to the regeneration of vital organs. Here, we report the engineering of 3D capillary beds in an in vitro microfluidic platform that is comprised of a biocompatible collagen I gel supported by a mechanical framework of alginate beads. The engineered vessels have patent lumens, form robust ~1.5 mm capillary networks across the devices, and support the perfusion of 1 ?m fluorescent beads through them. In addition, the alginate beads offer a modular method to encapsulate and co-culture cells that either promote angiogenesis or require perfusion for cell viability in engineered tissue constructs. This laboratory-constructed vascular supply may be clinically significant for the engineering of capillary beds and higher order biological tissues in a scalable and modular manner. © 2012 Chan et al.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/161698
ISSN: 19326203
DOI: 10.1371/journal.pone.0050582
Rights: Attribution 4.0 International
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