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E-cadherin plays an essential role in collective directional migration of large epithelial sheets.

Authors
  • Li, Li
  • Hartley, Robert
  • Reiss, Bjoern
  • Sun, Yaohui
  • Pu, Jin
  • Wu, Dan
  • Lin, Francis
  • Hoang, Trung
  • Yamada, Soichiro
  • Jiang, Jianxin
  • Zhao, Min
Type
Published Article
Journal
Cellular and Molecular Life Sciences
Publisher
Springer-Verlag
Publication Date
July 2012
Volume
69
Issue
16
Pages
2779–2789
Identifiers
DOI: 10.1007/s00018-012-0951-3
PMID: 22410739
Source
Medline
License
Unknown

Abstract

In wound healing and development, large epithelial sheets migrate collectively, in defined directions, and maintain tight cell-cell adhesion. This type of movement ensures an essential function of epithelia, a barrier, which is lost when cells lose connection and move in isolation. Unless wounded, epithelial sheets in cultures normally do not have overall directional migration. Cell migration is mostly studied when cells are in isolation and in the absence of mature cell-cell adhesion; the mechanisms of the migration of epithelial sheets are less well understood. We used small electric fields (EFs) as a directional cue to instigate and guide migration of epithelial sheets. Significantly, cells in monolayer migrated far more efficiently and directionally than cells in isolation or smaller cell clusters. We demonstrated for the first time the group size-dependent directional migratory response in several types of epithelial cells. Gap junctions made a minimal contribution to the directional collective migration. Breaking down calcium-dependent cell-cell adhesion significantly reduced directional sheet migration. Furthermore, E-cadherin blocking antibodies abolished migration of cell sheets. Traction force analysis revealed an important role of forces that cells in the leading rows exert on the substratum. With EF, the traction forces of the leading edge cells coordinated in directional re-orientation. Our study thus identifies a novel mechanism--E-cadherin dependence and coordinated traction forces of leading cells in collective directional migration of large epithelial sheets.

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