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dc.contributor.authorSorce, Barbara
dc.contributor.authorEscobedo, Carlos
dc.contributor.authorToyoda, Yusuke
dc.contributor.authorCattin, Cedric J.
dc.contributor.authorNewton, Richard
dc.contributor.authorBanerjee, Indranil
dc.contributor.authorStettler, Alexander
dc.contributor.authorRoska, Botond
dc.contributor.authorEaton, Suzanne
dc.contributor.authorHyman, Anthony A.
dc.contributor.authorHierlemann, Andreas
dc.contributor.authorMuller, Daniel J.
dc.contributor.authorStewart, Martin P
dc.date.accessioned2016-01-14T01:14:21Z
dc.date.available2016-01-14T01:14:21Z
dc.date.issued2015-11
dc.date.submitted2015-02
dc.identifier.issn2041-1723
dc.identifier.urihttp://hdl.handle.net/1721.1/100828
dc.description.abstractLittle is known about how mitotic cells round against epithelial confinement. Here, we engineer micropillar arrays that subject cells to lateral mechanical confinement similar to that experienced in epithelia. If generating sufficient force to deform the pillars, rounding epithelial (MDCK) cells can create space to divide. However, if mitotic cells cannot create sufficient space, their rounding force, which is generated by actomyosin contraction and hydrostatic pressure, pushes the cell out of confinement. After conducting mitosis in an unperturbed manner, both daughter cells return to the confinement of the pillars. Cells that cannot round against nor escape confinement cannot orient their mitotic spindles and more likely undergo apoptosis. The results highlight how spatially constrained epithelial cells prepare for mitosis: either they are strong enough to round up or they must escape. The ability to escape from confinement and reintegrate after mitosis appears to be a basic property of epithelial cells.en_US
dc.description.sponsorshipSwiss National Science Foundation (Advanced Mobility Fellowship)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/ncomms9872en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNature Publishing Groupen_US
dc.titleMitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinementen_US
dc.typeArticleen_US
dc.identifier.citationSorce, Barbara, Carlos Escobedo, Yusuke Toyoda, Martin P. Stewart, Cedric J. Cattin, Richard Newton, Indranil Banerjee, et al. “Mitotic Cells Contract Actomyosin Cortex and Generate Pressure to Round Against or Escape Epithelial Confinement.” Nat Comms 6 (November 25, 2015): 8872. © 2015 Macmillan Publishers Limiteden_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorStewart, Martin P.en_US
dc.relation.journalNature Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsSorce, Barbara; Escobedo, Carlos; Toyoda, Yusuke; Stewart, Martin P.; Cattin, Cedric J.; Newton, Richard; Banerjee, Indranil; Stettler, Alexander; Roska, Botond; Eaton, Suzanne; Hyman, Anthony A.; Hierlemann, Andreas; Muller, Daniel J.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-4112-6622
mit.licenseOPEN_ACCESS_POLICYen_US


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