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dc.contributor.authorShin, Yoojin
dc.contributor.authorHan, Sewoon
dc.contributor.authorJeon, Jessie S.
dc.contributor.authorYamamoto, Kyoko
dc.contributor.authorZervantonakis, Ioannis K
dc.contributor.authorSudo, Ryo
dc.contributor.authorKamm, Roger Dale
dc.contributor.authorChung, Seok
dc.contributor.authorZervantonakis, Ioannis K.
dc.date.accessioned2014-06-09T20:30:06Z
dc.date.available2014-06-09T20:30:06Z
dc.date.issued2012-06
dc.identifier.issn1754-2189
dc.identifier.issn1750-2799
dc.identifier.urihttp://hdl.handle.net/1721.1/87711
dc.description.abstractThis protocol describes a simple but robust microfluidic assay combining three-dimensional (3D) and two-dimensional (2D) cell culture. The microfluidic platform comprises hydrogel-incorporating chambers between surface-accessible microchannels. By using this platform, well-defined biochemical and biophysical stimuli can be applied to multiple cell types interacting over distances of <1 mm, thereby replicating many aspects of the in vivo microenvironment. Capabilities exist for time-dependent manipulation of flow and concentration gradients as well as high-resolution real-time imaging for observing spatial-temporal single-cell behavior, cell-cell communication, cell-matrix interactions and cell population dynamics. These heterotypic cell type assays can be used to study cell survival, proliferation, migration, morphogenesis and differentiation under controlled conditions. Applications include the study of previously unexplored cellular interactions, and they have already provided new insights into how biochemical and biophysical factors regulate interactions between populations of different cell types. It takes 3 d to fabricate the system and experiments can run for up to several weeks.en_US
dc.description.sponsorshipNational Research Foundation of Korea (grant no. 2010-0023975)en_US
dc.description.sponsorshipJapan Society for the Promotion of Science (G2212)en_US
dc.description.sponsorshipJapan. Science and Technology Agency (22680037)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (CBET-0939511)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/nprot.2012.051en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleMicrofluidic assay for simultaneous culture of multiple cell types on surfaces or within hydrogelsen_US
dc.typeArticleen_US
dc.identifier.citationShin, Yoojin, Sewoon Han, Jessie S Jeon, Kyoko Yamamoto, Ioannis K Zervantonakis, Ryo Sudo, Roger D Kamm, and Seok Chung. “Microfluidic Assay for Simultaneous Culture of Multiple Cell Types on Surfaces or Within Hydrogels.” Nat Protoc 7, no. 7 (June 7, 2012): 1247–1259.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.mitauthorJeon, Jessie S.en_US
dc.contributor.mitauthorZervantonakis, Ioannis K.en_US
dc.contributor.mitauthorKamm, Roger Daleen_US
dc.relation.journalNature Protocolsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsShin, Yoojin; Han, Sewoon; Jeon, Jessie S; Yamamoto, Kyoko; Zervantonakis, Ioannis K; Sudo, Ryo; Kamm, Roger D; Chung, Seoken_US
dc.identifier.orcidhttps://orcid.org/0000-0002-7232-304X
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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