Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0050582
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dc.titleEngineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting
dc.contributor.authorChan J.M.
dc.contributor.authorZervantonakis I.K.
dc.contributor.authorRimchala T.
dc.contributor.authorPolacheck W.J.
dc.contributor.authorWhisler J.
dc.contributor.authorKamm R.D.
dc.date.accessioned2019-11-07T01:15:11Z
dc.date.available2019-11-07T01:15:11Z
dc.date.issued2012
dc.identifier.citationChan 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
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161698
dc.description.abstractIn 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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectalginic acid
dc.subjectcollagen type 1
dc.subjectangiogenesis
dc.subjectarticle
dc.subjectcapillary
dc.subjectcell viability
dc.subjectcoculture
dc.subjectcontrolled study
dc.subjectencapsulation
dc.subjectfibroblast
dc.subjectgel
dc.subjectgenetic transfection
dc.subjecthuman
dc.subjecthuman cell
dc.subjectimmunocytochemistry
dc.subjectin vitro study
dc.subjectmicrofluidics
dc.subjectperfusion
dc.subjectplasmid
dc.subjectself directed angiogenic sprouting
dc.subjecttissue engineering
dc.subjectAlginates
dc.subjectCapillaries
dc.subjectCells, Cultured
dc.subjectCoculture Techniques
dc.subjectGlucuronic Acid
dc.subjectHexuronic Acids
dc.subjectHumans
dc.subjectImmunohistochemistry
dc.subjectMicrofluidics
dc.subjectNeovascularization, Physiologic
dc.subjectTissue Scaffolds
dc.typeArticle
dc.contributor.departmentSURGERY
dc.description.doi10.1371/journal.pone.0050582
dc.description.sourcetitlePLoS ONE
dc.description.volume7
dc.description.issue12
dc.description.pagee50582
dc.published.statePublished
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