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dc.contributor.authorYamamoto, Kyoko
dc.contributor.authorTanimura, Kohei
dc.contributor.authorWatanabe, Masafumi
dc.contributor.authorSano, Hiromu
dc.contributor.authorUwamori, Hiroyuki
dc.contributor.authorMabuchi, Yo
dc.contributor.authorMatsuzaki, Yumi
dc.contributor.authorChung, Seok
dc.contributor.authorKamm, Roger Dale
dc.contributor.authorTanishita, Kazuo
dc.contributor.authorSudo, Ryo
dc.date.accessioned2020-04-09T14:45:51Z
dc.date.available2020-04-09T14:45:51Z
dc.date.issued2018-10
dc.date.submitted2018-07
dc.identifier.issn1937-3341
dc.identifier.issn1937-335X
dc.identifier.urihttps://hdl.handle.net/1721.1/124556
dc.description.abstractConstruction of small and continuous capillary networks is a fundamental challenge for the development of three-dimensional (3D) tissue engineering. In particular, to construct mature and stable capillary networks, it is important to consider interactions between endothelial cells and pericytes. This study aimed to construct stable capillary networks covered by pericyte-like perivascular cells, which maintain the lumen of small diameter similar to that of capillary structures in vivo. Vascular sprouting, capillary extension, and stabilization were investigated using a 3D angiogenesis model containing human umbilical vein endothelial cells (HUVECs) and mesenchymal stem cells (MSCs) in a microfluidic device. A series of HUVEC:MSC ratios was tested; the ratio was found to be an important factor in the construction of capillary structures. We found that stable capillary networks that were covered by MSC-derived perivascular cells can be constructed at 1:1 HUVEC:MSC ratio. The constructed capillary networks had continuous lumens with <10-μm diameter, which were maintained for at least 21 days. This angiogenic process and basement membrane formation were regulated by HUVEC-MSC interactions. Construction of capillary networks is a fundamental challenge for the development of three-dimensional (3D) tissue engineering. However, it is not well understood how to construct stable capillary networks that maintain a luminal size similar to that of capillary structures in vivo (i.e., <10 μm diameter). In this study, we demonstrated the construction of stable capillary networks covered by pericyte-like perivascular cells using an in vitro 3D angiogenesis model by optimizing interactions between endothelial cells and perivascular cells. Our 3D angiogenesis model can be combined with 3D culture of epithelial cells in the context of vascularization of 3D tissue-engineered constructs. Keywords:3D angiogenesis model; microfluidic device; pericytes; mesenchymal stem cellsen_US
dc.description.sponsorshipJapan Society for Promotion of Science (16H03173 and 25560208)en_US
dc.language.isoen
dc.publisherMary Ann Liebert Incen_US
dc.relation.isversionofhttp://dx.doi.org/10.1089/ten.tea.2018.0186en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceMary Ann Lieberten_US
dc.titleConstruction of Continuous Capillary Networks Stabilized by Pericyte-like Perivascular Cellsen_US
dc.typeArticleen_US
dc.identifier.citationYamamoto, Kyoko et al. "Construction of Continuous Capillary Networks Stabilized by Pericyte-like Perivascular Cells." Tissue Engineering Part A 25, 5-6 (March 2019): 499-510 ©2019, Mary Ann Liebert, Inc.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalTissue Engineering Part Aen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-09-17T13:25:38Z
dspace.date.submission2019-09-17T13:25:40Z
mit.journal.volume25en_US
mit.journal.issue5-6en_US
mit.metadata.statusComplete


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