Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pone.0050582
DC Field | Value | |
---|---|---|
dc.title | Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting | |
dc.contributor.author | Chan J.M. | |
dc.contributor.author | Zervantonakis I.K. | |
dc.contributor.author | Rimchala T. | |
dc.contributor.author | Polacheck W.J. | |
dc.contributor.author | Whisler J. | |
dc.contributor.author | Kamm R.D. | |
dc.date.accessioned | 2019-11-07T01:15:11Z | |
dc.date.available | 2019-11-07T01:15:11Z | |
dc.date.issued | 2012 | |
dc.identifier.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 | |
dc.identifier.issn | 19326203 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/161698 | |
dc.description.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. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20191101 | |
dc.subject | alginic acid | |
dc.subject | collagen type 1 | |
dc.subject | angiogenesis | |
dc.subject | article | |
dc.subject | capillary | |
dc.subject | cell viability | |
dc.subject | coculture | |
dc.subject | controlled study | |
dc.subject | encapsulation | |
dc.subject | fibroblast | |
dc.subject | gel | |
dc.subject | genetic transfection | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | immunocytochemistry | |
dc.subject | in vitro study | |
dc.subject | microfluidics | |
dc.subject | perfusion | |
dc.subject | plasmid | |
dc.subject | self directed angiogenic sprouting | |
dc.subject | tissue engineering | |
dc.subject | Alginates | |
dc.subject | Capillaries | |
dc.subject | Cells, Cultured | |
dc.subject | Coculture Techniques | |
dc.subject | Glucuronic Acid | |
dc.subject | Hexuronic Acids | |
dc.subject | Humans | |
dc.subject | Immunohistochemistry | |
dc.subject | Microfluidics | |
dc.subject | Neovascularization, Physiologic | |
dc.subject | Tissue Scaffolds | |
dc.type | Article | |
dc.contributor.department | SURGERY | |
dc.description.doi | 10.1371/journal.pone.0050582 | |
dc.description.sourcetitle | PLoS ONE | |
dc.description.volume | 7 | |
dc.description.issue | 12 | |
dc.description.page | e50582 | |
dc.published.state | Published | |
Appears in Collections: | Staff Publications Elements |
Show simple item record
Files in This Item:
File | Description | Size | Format | Access Settings | Version | |
---|---|---|---|---|---|---|
10_1371_journal_pone_0050582.pdf | 6.68 MB | Adobe PDF | OPEN | None | View/Download |
This item is licensed under a Creative Commons License