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A Novel In Vitro Model for Microvasculature Reveals Regulation of Circumferential ECM Organization by Curvature

In microvascular vessels, endothelial cells are aligned longitudinally whereas several components of the extracellular matrix (ECM) are organized circumferentially. While current three-dimensional (3D) in vitro models for microvasculature have allowed the study of ECM-regulated tubulogenesis, they h...

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Autores principales: Barreto-Ortiz, Sebastian F., Zhang, Shuming, Davenport, Matthew, Fradkin, Jamie, Ginn, Brian, Mao, Hai-Quan, Gerecht, Sharon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836741/
https://www.ncbi.nlm.nih.gov/pubmed/24278378
http://dx.doi.org/10.1371/journal.pone.0081061
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author Barreto-Ortiz, Sebastian F.
Zhang, Shuming
Davenport, Matthew
Fradkin, Jamie
Ginn, Brian
Mao, Hai-Quan
Gerecht, Sharon
author_facet Barreto-Ortiz, Sebastian F.
Zhang, Shuming
Davenport, Matthew
Fradkin, Jamie
Ginn, Brian
Mao, Hai-Quan
Gerecht, Sharon
author_sort Barreto-Ortiz, Sebastian F.
collection PubMed
description In microvascular vessels, endothelial cells are aligned longitudinally whereas several components of the extracellular matrix (ECM) are organized circumferentially. While current three-dimensional (3D) in vitro models for microvasculature have allowed the study of ECM-regulated tubulogenesis, they have limited control over topographical cues presented by the ECM and impart a barrier for the high-resolution and dynamic study of multicellular and extracellular organization. Here we exploit a 3D fibrin microfiber scaffold to develop a novel in vitro model of the microvasculature that recapitulates endothelial alignment and ECM deposition in a setting that also allows the sequential co-culture of mural cells. We show that the microfibers' nanotopography induces longitudinal adhesion and alignment of endothelial colony-forming cells (ECFCs), and that these deposit circumferentially organized ECM. We found that ECM wrapping on the microfibers is independent of ECFCs' actin and microtubule organization, but it is dependent on the curvature of the microfiber. Microfibers with smaller diameters (100–400 µm) guided circumferential ECM deposition, whereas microfibers with larger diameters (450 µm) failed to support wrapping ECM. Finally, we demonstrate that vascular smooth muscle cells attached on ECFC-seeded microfibers, depositing collagen I and elastin. Collectively, we establish a novel in vitro model for the sequential control and study of microvasculature development and reveal the unprecedented role of the endothelium in organized ECM deposition regulated by the microfiber curvature.
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spelling pubmed-38367412013-11-25 A Novel In Vitro Model for Microvasculature Reveals Regulation of Circumferential ECM Organization by Curvature Barreto-Ortiz, Sebastian F. Zhang, Shuming Davenport, Matthew Fradkin, Jamie Ginn, Brian Mao, Hai-Quan Gerecht, Sharon PLoS One Research Article In microvascular vessels, endothelial cells are aligned longitudinally whereas several components of the extracellular matrix (ECM) are organized circumferentially. While current three-dimensional (3D) in vitro models for microvasculature have allowed the study of ECM-regulated tubulogenesis, they have limited control over topographical cues presented by the ECM and impart a barrier for the high-resolution and dynamic study of multicellular and extracellular organization. Here we exploit a 3D fibrin microfiber scaffold to develop a novel in vitro model of the microvasculature that recapitulates endothelial alignment and ECM deposition in a setting that also allows the sequential co-culture of mural cells. We show that the microfibers' nanotopography induces longitudinal adhesion and alignment of endothelial colony-forming cells (ECFCs), and that these deposit circumferentially organized ECM. We found that ECM wrapping on the microfibers is independent of ECFCs' actin and microtubule organization, but it is dependent on the curvature of the microfiber. Microfibers with smaller diameters (100–400 µm) guided circumferential ECM deposition, whereas microfibers with larger diameters (450 µm) failed to support wrapping ECM. Finally, we demonstrate that vascular smooth muscle cells attached on ECFC-seeded microfibers, depositing collagen I and elastin. Collectively, we establish a novel in vitro model for the sequential control and study of microvasculature development and reveal the unprecedented role of the endothelium in organized ECM deposition regulated by the microfiber curvature. Public Library of Science 2013-11-21 /pmc/articles/PMC3836741/ /pubmed/24278378 http://dx.doi.org/10.1371/journal.pone.0081061 Text en © 2013 Barreto-Ortiz 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
Barreto-Ortiz, Sebastian F.
Zhang, Shuming
Davenport, Matthew
Fradkin, Jamie
Ginn, Brian
Mao, Hai-Quan
Gerecht, Sharon
A Novel In Vitro Model for Microvasculature Reveals Regulation of Circumferential ECM Organization by Curvature
title A Novel In Vitro Model for Microvasculature Reveals Regulation of Circumferential ECM Organization by Curvature
title_full A Novel In Vitro Model for Microvasculature Reveals Regulation of Circumferential ECM Organization by Curvature
title_fullStr A Novel In Vitro Model for Microvasculature Reveals Regulation of Circumferential ECM Organization by Curvature
title_full_unstemmed A Novel In Vitro Model for Microvasculature Reveals Regulation of Circumferential ECM Organization by Curvature
title_short A Novel In Vitro Model for Microvasculature Reveals Regulation of Circumferential ECM Organization by Curvature
title_sort novel in vitro model for microvasculature reveals regulation of circumferential ecm organization by curvature
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836741/
https://www.ncbi.nlm.nih.gov/pubmed/24278378
http://dx.doi.org/10.1371/journal.pone.0081061
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