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Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting

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 d...

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Autores principales: Chan, Juliana M., Zervantonakis, Ioannis K., Rimchala, Tharathorn, Polacheck, William J., Whisler, Jordan, Kamm, Roger D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514279/
https://www.ncbi.nlm.nih.gov/pubmed/23226527
http://dx.doi.org/10.1371/journal.pone.0050582
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author Chan, Juliana M.
Zervantonakis, Ioannis K.
Rimchala, Tharathorn
Polacheck, William J.
Whisler, Jordan
Kamm, Roger D.
author_facet Chan, Juliana M.
Zervantonakis, Ioannis K.
Rimchala, Tharathorn
Polacheck, William J.
Whisler, Jordan
Kamm, Roger D.
author_sort Chan, Juliana M.
collection PubMed
description 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 µm 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.
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spelling pubmed-35142792012-12-05 Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting Chan, Juliana M. Zervantonakis, Ioannis K. Rimchala, Tharathorn Polacheck, William J. Whisler, Jordan Kamm, Roger D. PLoS One Research Article 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 µm 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. Public Library of Science 2012-12-04 /pmc/articles/PMC3514279/ /pubmed/23226527 http://dx.doi.org/10.1371/journal.pone.0050582 Text en © 2012 Chan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chan, Juliana M.
Zervantonakis, Ioannis K.
Rimchala, Tharathorn
Polacheck, William J.
Whisler, Jordan
Kamm, Roger D.
Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting
title Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting
title_full Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting
title_fullStr Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting
title_full_unstemmed Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting
title_short Engineering of In Vitro 3D Capillary Beds by Self-Directed Angiogenic Sprouting
title_sort engineering of in vitro 3d capillary beds by self-directed angiogenic sprouting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514279/
https://www.ncbi.nlm.nih.gov/pubmed/23226527
http://dx.doi.org/10.1371/journal.pone.0050582
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