Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-017-01390-x
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dc.titleEmergent patterns of collective cell migration under tubular confinement
dc.contributor.authorXi, W
dc.contributor.authorSonam, S
dc.contributor.authorBeng Saw, T
dc.contributor.authorLadoux, B
dc.contributor.authorTeck Lim, C
dc.date.accessioned2020-09-04T03:30:52Z
dc.date.available2020-09-04T03:30:52Z
dc.date.issued2017
dc.identifier.citationXi, W, Sonam, S, Beng Saw, T, Ladoux, B, Teck Lim, C (2017). Emergent patterns of collective cell migration under tubular confinement. Nature Communications 8 (1) : 1517. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-017-01390-x
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174386
dc.description.abstractCollective epithelial behaviors are essential for the development of lumens in organs. However, conventional assays of planar systems fail to replicate cell cohorts of tubular structures that advance in concerted ways on out-of-plane curved and confined surfaces, such as ductal elongation in vivo. Here, we mimic such coordinated tissue migration by forming lumens of epithelial cell sheets inside microtubes of 1-10 cell lengths in diameter. We show that these cell tubes reproduce the physiological apical-basal polarity, and have actin alignment, cell orientation, tissue organization, and migration modes that depend on the extent of tubular confinement and/or curvature. In contrast to flat constraint, the cell sheets in a highly constricted smaller microtube demonstrate slow motion with periodic relaxation, but fast overall movement in large microtubes. Altogether, our findings provide insights into the emerging migratory modes for epithelial migration and growth under tubular confinement, which are reminiscent of the in vivo scenario. © 2017 The Author(s).
dc.publisherNature Publishing Group
dc.sourceUnpaywall 20200831
dc.subjectactin
dc.subjectbaysilon
dc.subjectdimeticone
dc.subjectanatomy
dc.subjectcells and cell components
dc.subjectdevelopmental biology
dc.subjectdiameter
dc.subjectgrowth
dc.subjectmovement
dc.subjectphysiology
dc.subjectprotein
dc.subjectscenario analysis
dc.subjectanimal cell
dc.subjectArticle
dc.subjectcell junction
dc.subjectcell migration
dc.subjectcell polarity
dc.subjectcell proliferation
dc.subjectepithelium
dc.subjectMDCK cell line
dc.subjectmicrotubule
dc.subjectnonhuman
dc.subjectalgorithm
dc.subjectanimal
dc.subjectbiological model
dc.subjectcell adhesion
dc.subjectcell line
dc.subjectcell motion
dc.subjectdog
dc.subjectepithelium cell
dc.subjecthuman
dc.subjectmetabolism
dc.subjectphysiology
dc.subjectAlgorithms
dc.subjectAnimals
dc.subjectCell Adhesion
dc.subjectCell Line
dc.subjectCell Movement
dc.subjectDimethylpolysiloxanes
dc.subjectDogs
dc.subjectEpithelial Cells
dc.subjectHumans
dc.subjectMadin Darby Canine Kidney Cells
dc.subjectMicrotubules
dc.subjectModels, Biological
dc.typeArticle
dc.contributor.departmentCENTRE FOR ADVANCED 2D MATERIALS
dc.contributor.departmentMECHANOBIOLOGY INSTITUTE
dc.contributor.departmentBIOLOGY (NU)
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1038/s41467-017-01390-x
dc.description.sourcetitleNature Communications
dc.description.volume8
dc.description.issue1
dc.description.page1517
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