E-cadherin junction formation involves an active kinetic nucleation process

  • Kabir H. Biswas
  • , Kevin L. Hartman
  • , Cheng Han Yu
  • , Oliver J. Harrison
  • , Hang Song
  • , Adam W. Smith
  • , William Y.C. Huang
  • , Wan Chen Lin
  • , Zhenhuan Guo
  • , Anup Padmanabhan
  • , Sergey M. Troyanovsky
  • , Michael L. Dustin
  • , Lawrence Shapiro
  • , Barry Honig*
  • , Ronen Zaidel-Bar
  • , Jay T. Groves
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Epithelial (E)-cadherin-mediated cell - cell junctions play important roles in the development and maintenance of tissue structure in multicellular organisms. E-cadherin adhesion is thus a key element of the cellular microenvironment that provides both mechanical and biochemical signaling inputs. Here, we report in vitro reconstitution of junction-like structures between native E-cadherin in living cells and the extracellular domain of E-cadherin (E-cad-ECD) in a supported membrane. Junction formation in this hybrid live cell-supported membrane configuration requires both active processes within the living cell and a supported membrane with low E-cad-ECD mobility. The hybrid junctions recruit α-catenin and exhibit remodeled cortical actin. Observations suggest that the initial stages of junction formation in this hybrid system depend on the trans but not the cis interactions between E-cadherin molecules, and proceed via a nucleation process in which protrusion and retraction of filopodia play a key role.

Original languageEnglish
Pages (from-to)10932-10937
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume112
Issue number35
DOIs
Publication statusPublished - 1 Sept 2015
Externally publishedYes

Keywords

  • Adhesion
  • Bilayer
  • Cadherin
  • Diffusion
  • Nucleation

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