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dc.date.accessioned2019-12-09T20:26:12Z
dc.date.available2019-12-09T20:26:12Z
dc.date.created2018-11-12T12:49:33Z
dc.date.issued2018
dc.identifier.citationLång, Emma Helena Polec, Anna Lång, Anna Ulrika Valk, Marijke Blicher, Pernille Rowe, Alexander D. Tønseth, Kim Alexander Jackson, Catherine Utheim, Tor Paaske Janssen, Liesbeth M.C. Eriksson, Jens Christian Bøe, Stig Ove . Coordinated collective migration and asymmetric cell division in confluent human keratinocytes without wounding. Nature Communications. 2018, 9:3665, 1-15
dc.identifier.urihttp://hdl.handle.net/10852/71481
dc.description.abstractEpithelial sheet spreading is a fundamental cellular process that must be coordinated with cell division and differentiation to restore tissue integrity. Here we use consecutive serum deprivation and re-stimulation to reconstruct biphasic collective migration and proliferation in cultured sheets of human keratinocytes. In this system, a burst of long-range coordinated locomotion is rapidly generated throughout the cell sheet in the absence of wound edges. Migrating cohorts reach correlation lengths of several millimeters and display dependencies on epidermal growth factor receptor-mediated signaling, self-propelled polarized migration, and a G1/G0 cell cycle environment. The migration phase is temporally and spatially aligned with polarized cell divisions characterized by pre-mitotic nuclear migration to the cell front and asymmetric partitioning of nuclear promyelocytic leukemia bodies and lysosomes to opposite daughter cells. This study investigates underlying mechanisms contributing to the stark contrast between cells in a static quiescent state compared to the long-range coordinated collective migration seen in contact with blood serum.en_US
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleCoordinated collective migration and asymmetric cell division in confluent human keratinocytes without woundingen_US
dc.typeJournal articleen_US
dc.creator.authorLång, Emma Helena
dc.creator.authorPolec, Anna
dc.creator.authorLång, Anna Ulrika
dc.creator.authorValk, Marijke
dc.creator.authorBlicher, Pernille
dc.creator.authorRowe, Alexander D.
dc.creator.authorTønseth, Kim Alexander
dc.creator.authorJackson, Catherine
dc.creator.authorUtheim, Tor Paaske
dc.creator.authorJanssen, Liesbeth M.C.
dc.creator.authorEriksson, Jens Christian
dc.creator.authorBøe, Stig Ove
cristin.unitcode185,53,18,14
cristin.unitnameAvdeling for medisinsk biokjemi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1629450
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Nature Communications&rft.volume=9:3665&rft.spage=1&rft.date=2018
dc.identifier.jtitleNature Communications
dc.identifier.volume9:3665
dc.identifier.startpage1
dc.identifier.endpage15
dc.identifier.doihttps://doi.org/10.1038/s41467-018-05578-7
dc.identifier.urnURN:NBN:no-74591
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn2041-1723
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/71481/2/Coordinated%2Bcollective%2Bmigration%2Band%2Basymmetric%2Bcell%2Bdivision.pdf
dc.type.versionPublishedVersion


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