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Ultrastructure and cell-cell coupling of cardiac myocytes differentiating in embryonic stem cell cultures

dc.contributor.authorWestfall, Margaret V.en_US
dc.contributor.authorPasyk, Krystyna A.en_US
dc.contributor.authorYule, David I.en_US
dc.contributor.authorSamuelson, Linda C.en_US
dc.contributor.authorMetzger, Joseph M.en_US
dc.date.accessioned2006-04-19T14:01:19Z
dc.date.available2006-04-19T14:01:19Z
dc.date.issued1997en_US
dc.identifier.citationWestfall, Margaret V.; Pasyk, Krystyna A.; Yule, David I.; Samuelson, Linda C.; Metzger, Joseph M. (1997)."Ultrastructure and cell-cell coupling of cardiac myocytes differentiating in embryonic stem cell cultures." Cell Motility and the Cytoskeleton 36(1): 43-54. <http://hdl.handle.net/2027.42/34963>en_US
dc.identifier.issn0886-1544en_US
dc.identifier.issn1097-0169en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34963
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8986376&dopt=citationen_US
dc.description.abstractDifferentiation cultures of embryonic stem (ES) cells can be a useful in vitro system for understanding cardiac myocyte development. However, cell morphometry, sarcomere development, and functional cell-cell junction formation have not been examined in detail to determine whether ES cell-derived cardiac myocytes exhibit structural and functional characteristics similar to cardiac myocytes within the developing heart. Therefore, we examined cellular dimensions, sarcomere formation, and cell-cell contacts in differentiating cardiac myocytes derived from mouse D3-ES cell cultures. Cells exhibited rod-shaped morphology and had single centrally located nuclei, typical of maturing cardiac myocytes. The cellular dimensions of 59 individual cardiac myocytes within contracting foci of ES cell cultures were analyzed (length = 42.2 ± 2.1 μm, area = 197 ± 19 μm 2 , and diameter = 5.5 ± 0.3 μm) and found to be similar to myocytes in vivo. Transmission electron micrographs of ES cell-derived cardiac myocytes indicated myofibrillar architecture ranged from sparse and disorganized to densely packed, parallel arrays of myofibrils organized into mature sarcomeres. This pattern of myofibrillar assembly in maturing sarcomeres was similar to that observed during in vivo myocyte differentiation. Another hallmark of cardiac development is the formation of intercalated discs, which functionally couple adjacent cardiac myocytes. Electron micrographs indicated nascent intercalated discs were forming in foci of ES cell-derived cardiac myocytes. In addition, indirect immunostaining with anti-connexin 43 antibody (Ab), a monoclonal Ab to the gap junction component of the intercalated disc, indicated that gap junctions were present in contracting ES cell foci. Furthermore, microinjection of single cardiac myocytes with Lucifer yellow (2.5 μM) resulted in the spread of fluorescence to adjacent cells within a contracting focus, an indication of functional cell-cell coupling across these gap junctions. Together, these results indicate ES cell-derived cardiac myocytes exhibit cell morphology, sarcomere formation, and cell-cell junctions similar to those observed in cardiac myocytes developing in vivo. Cell Motil. Cytoskeleton 36:43–54, 1997. © 1997 Wiley-Liss, Inc.en_US
dc.format.extent874203 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCell & Developmental Biologyen_US
dc.titleUltrastructure and cell-cell coupling of cardiac myocytes differentiating in embryonic stem cell culturesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Physiology, University of Michigan, Ann Arbor, Michigan ; Dept. of Physiology, 7730 Med. Sci. II, 1301 E. Catherine St., University of Michigan, Ann Arbor, MI 48109-0622en_US
dc.contributor.affiliationumDepartment of Physiology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Physiology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Physiology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Physiology, University of Michigan, Ann Arbor, Michiganen_US
dc.identifier.pmid8986376en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34963/1/4_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1097-0169(1997)36:1<43::AID-CM4>3.0.CO;2-Ien_US
dc.identifier.sourceCell Motility and the Cytoskeletonen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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