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dc.contributor.authorChaturvedi, Ritika R.
dc.contributor.authorSolorzano, Ricardo D.
dc.contributor.authorEyckmans, Jeroen
dc.contributor.authorBaranski, Jan D.
dc.contributor.authorStapleton, Sarah Chase
dc.contributor.authorStevens, Kelly R.
dc.contributor.authorBhatia, Sangeeta N
dc.contributor.authorChen, Christopher S.
dc.contributor.authorSchwartz, Robert E.
dc.date.accessioned2017-07-18T18:05:23Z
dc.date.available2017-07-18T18:05:23Z
dc.date.issued2015-02
dc.identifier.issn1937-3384
dc.identifier.issn1937-3392
dc.identifier.urihttp://hdl.handle.net/1721.1/110769
dc.description.abstractThe ultimate design of functionally therapeutic engineered tissues and organs will rely on our ability to engineer vasculature that can meet tissue-specific metabolic needs. We recently introduced an approach for patterning the formation of functional spatially organized vascular architectures within engineered tissues in vivo. Here, we now explore the design parameters of this approach and how they impact the vascularization of an engineered tissue construct after implantation. We used micropatterning techniques to organize endothelial cells (ECs) into geometrically defined “cords,” which in turn acted as a template after implantation for the guided formation of patterned capillaries integrated with the host tissue. We demonstrated that the diameter of the cords before implantation impacts the location and density of the resultant capillary network. Inclusion of mural cells to the vascularization response appears primarily to impact the dynamics of vascularization. We established that clinically relevant endothelial sources such as induced pluripotent stem cell-derived ECs and human microvascular endothelial cells can drive vascularization within this system. Finally, we demonstrated the ability to control the juxtaposition of parenchyma with perfused vasculature by implanting cords containing a mixture of both a parenchymal cell type (hepatocytes) and ECs. These findings define important characteristics that will ultimately impact the design of vasculature structures that meet tissue-specific needs.en_US
dc.description.sponsorshipNational Institute of Biomedical Imaging and Bioengineering (U.S.) (Award Number EB000262)en_US
dc.description.sponsorshipNational Institute of Biomedical Imaging and Bioengineering (U.S.) (Award Number EB08396)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.). National Research Service Awards (1F32DK091007)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.). National Research Service Awards (5T32AR007132-35)en_US
dc.language.isoen_US
dc.publisherMary Ann Liebert, Inc.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1089/ten.tec.2014.0258en_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.titlePatterning Vascular Networks In Vivo for Tissue Engineering Applicationsen_US
dc.typeArticleen_US
dc.identifier.citationChaturvedi, Ritika R., Kelly R. Stevens, Ricardo D. Solorzano, Robert E. Schwartz, Jeroen Eyckmans, Jan D. Baranski, Sarah Chase Stapleton, Sangeeta N. Bhatia, and Christopher S. Chen. “Patterning Vascular NetworksIn Vivofor Tissue Engineering Applications.” Tissue Engineering Part C: Methods 21, no. 5 (May 2015): 509–517.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.mitauthorStevens, Kelly R.
dc.contributor.mitauthorSchwartz, Robert E
dc.contributor.mitauthorBhatia, Sangeeta N
dc.contributor.mitauthorChen, Christopher S.
dc.relation.journalTissue Engineering Part C: Methodsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsChaturvedi, Ritika R.; Stevens, Kelly R.; Solorzano, Ricardo D.; Schwartz, Robert E.; Eyckmans, Jeroen; Baranski, Jan D.; Stapleton, Sarah Chase; Bhatia, Sangeeta N.; Chen, Christopher S.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-1293-2097
mit.licensePUBLISHER_POLICYen_US


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