p120-catenin controls contractility along the vertical axis of epithelial lateral membranes.

Yu HH, Dohn MR, Markham NO, Coffey RJ, Reynolds AB
J Cell Sci. 2016 129 (1): 80-94

PMID: 26585313 · PMCID: PMC4732297 · DOI:10.1242/jcs.177550

In vertebrate epithelia, p120-catenin (hereafter referred to as p120; also known as CTNND1) mediates E-cadherin stability and suppression of RhoA. Genetic ablation of p120 in various epithelial tissues typically causes striking alterations in tissue function and morphology. Although these effects could very well involve p120's activity towards Rho, ascertaining the impact of this relationship has been complicated by the fact that p120 is also required for cell-cell adhesion. Here, we have molecularly uncoupled p120's cadherin-stabilizing and RhoA-suppressing activites. Unexpectedly, removing p120's Rho-suppressing activity dramatically disrupted the integrity of the apical surface, irrespective of E-cadherin stability. The physical defect was tracked to excessive actomyosin contractility along the vertical axis of lateral membranes. Thus, we suggest that p120's distinct activities towards E-cadherin and Rho are molecularly and functionally coupled and this, in turn, enables the maintenance of cell shape in the larger context of an epithelial monolayer. Importantly, local suppression of contractility by cadherin-bound p120 appears to go beyond regulating cell shape, as loss of this activity also leads to major defects in epithelial lumenogenesis.

© 2016. Published by The Company of Biologists Ltd.

MeSH Terms (16)

Amino Acid Sequence Animals Cadherins Catenins Cell Membrane Cell Polarity Cell Shape Dogs Epithelial Cells Madin Darby Canine Kidney Cells Molecular Sequence Data Nonmuscle Myosin Type IIA Phenotype Protein Binding rho-Associated Kinases rhoA GTP-Binding Protein

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