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dc.contributor.authorBae, Hojae
dc.contributor.authorHwang, Yu-Shik
dc.contributor.authorKwon, Il Keun
dc.contributor.authorSadr, Nasser
dc.contributor.authorManoucheri, Sam
dc.contributor.authorEdalat, Faramarz
dc.contributor.authorKim, Keekyoung
dc.contributor.authorKhademhosseini, Alireza
dc.contributor.authorCha, Jae Min
dc.contributor.authorKim, Sang Bok
dc.date.accessioned2016-12-02T20:26:38Z
dc.date.available2016-12-02T20:26:38Z
dc.date.issued2015-03
dc.date.submitted2014-12
dc.identifier.issn1598-5032
dc.identifier.issn2092-7673
dc.identifier.urihttp://hdl.handle.net/1721.1/105540
dc.description.abstractEmbryoid bodies have a number of similarities with cells in gastrulation, which provides useful biological information about embryonic stem cell differentiation. Extensive research has been done to study the control of embryoid body-mediated embryonic stem cell differentiation in various research fields. Recently, microengineering technology has been used to control the size of embryoid bodies and to direct lineage specific differentiation of embryonic stem cells. However, the underlying biology of developmental events in the embryoid bodies of different sizes has not been well elucidated. In this study, embryoid bodies with different sizes were generated within microfabricated PEG microwell arrays, and a series of gene and molecular expressions related to early developmental events was investigated to further elucidate the size-mediated differentiation. The gene and molecular expression profile suggested preferential visceral endoderm formation in 450 μm embryoid bodies and preferential lateral plate mesoderm formation in 150 μm embryoid bodies. These aggregates resulted in higher cardiac differentiation in 450 μm embryoid bodies and higher endothelial differentiation in 150 μm embryoid bodies, respectively. Our findings may provide further insight for understanding embryoid body size-mediated developmental progress.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (CAREER Award DMR0847287)en_US
dc.description.sponsorshipUnited States. Office of Naval Research (Naval Research Young National Investigator Award)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (HL092836, EB02597, AR057837)en_US
dc.publisherThe Polymer Society of Koreaen_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/s13233-015-3034-0en_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.sourceThe Polymer Society of Koreaen_US
dc.titleEmbryoid body size-mediated differential endodermal and mesodermal differentiation using polyethylene glycol (PEG) microwell arrayen_US
dc.typeArticleen_US
dc.identifier.citationCha, Jae Min, Hojae Bae, Nasser Sadr, Sam Manoucheri, Faramarz Edalat, Keekyoung Kim, Sang Bok Kim, Il Keun Kwon, Yu-Shik Hwang, and Ali Khademhosseini. “Embryoid Body Size-Mediated Differential Endodermal and Mesodermal Differentiation Using Polyethylene Glycol (PEG) Microwell Array.” Macromolecular Research 23, no. 3 (March 2015): 245–255.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.mitauthorSadr, Nasser
dc.contributor.mitauthorManoucheri, Sam
dc.contributor.mitauthorEdalat, Faramarz
dc.contributor.mitauthorKim, Keekyoung
dc.contributor.mitauthorKhademhosseini, Alireza
dc.contributor.mitauthorCha, Jae Min
dc.contributor.mitauthorKim, Sang Bok
dc.relation.journalMacromolecular Researchen_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
dc.date.updated2016-08-18T15:47:17Z
dc.language.rfc3066en
dc.rights.holderThe Polymer Society of Korea and Springer Sciene+Business Media Dordrecht
dspace.orderedauthorsCha, Jae Min; Bae, Hojae; Sadr, Nasser; Manoucheri, Sam; Edalat, Faramarz; Kim, Keekyoung; Kim, Sang Bok; Kwon, Il Keun; Hwang, Yu-Shik; Khademhosseini, Alien_US
dspace.embargo.termsNen
mit.licensePUBLISHER_POLICYen_US


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