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dc.contributor.authorKim, Jinseok
dc.contributor.authorHwang, Yu-Shik
dc.contributor.authorChung, Alice Mira
dc.contributor.authorChung, Bong Geun
dc.contributor.authorKhademhosseini, Alireza
dc.date.accessioned2016-08-24T20:48:46Z
dc.date.available2016-08-24T20:48:46Z
dc.date.issued2012-07
dc.date.submitted2012-05
dc.identifier.issn1016-8478
dc.identifier.issn0219-1032
dc.identifier.urihttp://hdl.handle.net/1721.1/103971
dc.description.abstractCardiomyocytes are the fundamental cells of the heart and play an important role in engineering of tissue constructs for regenerative medicine and drug discovery. Therefore, the development of culture conditions that can be used to generate functional cardiomyocytes to form cardiac tissue may be of great interest. In this study, isolated neonatal rat cardiomyocytes were cultured with several culture conditions in vitro and characterized for cell proliferation, myofibril organization, and cardiac functionality by assessing cell morphology, immunocytochemical staining, and time-lapse confocal scanning microscopy. When cardiomyocytes were cultured in liver cell line derived conditioned medium without exogenous growth factors and cytokines, the cell proliferation increased, cell morphology was highly elongated, and subsequent myofibril organization was highly developed. These developed myofibril organization also showed high level of contractibility and synchronization, representing high functionality of cardiomyocytes. Interestingly, many of the known factors in hepatic conditioned medium, such as insulin-like growth factor II (IGFII), macrophage colony-stimulating factor (MCSF), leukemia inhibitory factor (LIF), did not show similar effects as the hepatic conditioned medium, suggesting the possibility of synergistic activity of the several soluble factors or the presence of unknown factors in hepatic conditioned medium. Finally, we demonstrated that our culture system could provide a potentially powerful tool for in vitro cardiac tissue organization and cardiac function study.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH DE019024)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant HL092836)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant EB007249)en_US
dc.description.sponsorshipKorea Institute of Science and Technology (KIST) (Institutional Program)en_US
dc.description.sponsorshipUnited States. Army. Corps of Engineersen_US
dc.publisherKorean Society for Molecular and Cellular Biology/SpringerNatureen_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/s10059-012-0019-0en_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.sourceKorean Society for Molecular and Cellular Biologyen_US
dc.titleLiver cell line derived conditioned medium enhances myofibril organization of primary rat cardiomyocytesen_US
dc.typeArticleen_US
dc.identifier.citationKim, Jinseok, Yu-Shik Hwang, Alice Mira Chung, Bong Geun Chung, and Ali Khademhosseini. “Liver Cell Line Derived Conditioned Medium Enhances Myofibril Organization of Primary Rat Cardiomyocytes.” Molecules and Cells 34, no. 2 (July 25, 2012): 149-158.en_US
dc.contributor.departmentInstitute for Medical Engineering and Scienceen_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorKhademhosseini, Alirezaen_US
dc.relation.journalMolecules and Cellsen_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.updated2016-08-18T15:18:12Z
dc.language.rfc3066en
dc.rights.holderThe Korean Society for Molecular and Cellular Biology and Springer Netherlands
dspace.embargo.termsNen
mit.licensePUBLISHER_POLICYen_US


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