E-cadherin junction formation involves an active kinetic nucleation process.

Proc Natl Acad Sci U S A

Mechanobiology Institute, National University of Singapore, Singapore 117411; Department of Chemistry, University of California, Berkeley, CA 94720; Howard Hughes Medical Institute, University of California, Berkeley, CA 94720; Physical Biosciences and Materials Sciences Divisions, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720

Published: September 2015

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4568248PMC
http://dx.doi.org/10.1073/pnas.1513775112DOI Listing

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