Please use this identifier to cite or link to this item:
|Title:||Cell crawling mediates collective cell migration to close undamaged epithelial gaps||Authors:||Anon, E.
|Keywords:||Epithelial cell migration
Madin-Darby canine kidney cells
Wound model assay
|Issue Date:||3-Jul-2012||Citation:||Anon, E., Serra-Picamal, X., Hersen, P., Gauthier, N.C., Sheetz, M.P., Trepat, X., Ladoux, B. (2012-07-03). Cell crawling mediates collective cell migration to close undamaged epithelial gaps. Proceedings of the National Academy of Sciences of the United States of America 109 (27) : 10891-10896. ScholarBank@NUS Repository. https://doi.org/10.1073/pnas.1117814109||Abstract:||Fundamental biological processes such as morphogenesis and wound healing involve the closure of epithelial gaps. Epithelial gap closure is commonly attributed either to the purse-string contraction of an intercellular actomyosin cable or to active cell migration, but the relative contribution of these two mechanisms remains unknown. Here we present a model experiment to systematically study epithelial closure in the absence of cell injury. We developed a pillar stencil approach to create well-defined gaps in terms of size and shape within an epithelial cell monolayer. Upon pillar removal, cells actively respond to the newly accessible free space by extending lamellipodia and migrating into the gap. The decrease of gap area over time is strikingly linear and shows two different regimes depending on the size of the gap. In large gaps, closure is dominated by lamellipodium-mediated cell migration. By contrast, closure of gaps smaller than 20 μm was affected by cell density and progressed independently of Rac, myosin light chain kinase, and Rho kinase, suggesting a passive physical mechanism. By changing the shape of the gap, we observed that low-curvature areas favored the appearance of lamellipodia, promoting faster closure. Altogether, our results reveal that the closure of epithelial gaps in the absence of cell injury is governed by the collective migration of cells through the activation of lamellipodium protrusion.||Source Title:||Proceedings of the National Academy of Sciences of the United States of America||URI:||http://scholarbank.nus.edu.sg/handle/10635/100221||ISSN:||00278424||DOI:||10.1073/pnas.1117814109|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jun 26, 2019
WEB OF SCIENCETM
checked on Jun 26, 2019
checked on May 25, 2019
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.