Identification of a new regulation pathway of EGFR and E-cadherin dynamics

Sci Rep. 2021 Nov 22;11(1):22705. doi: 10.1038/s41598-021-02042-3.

Abstract

E-cadherin and EGFR are known to be closely associated hence regulating differentiation and proliferation notably in epithelia. We have previously shown that galectin-7 binds to E-cadherin and favors its retention at the plasma membrane. In this study, we shed in light that galectin-7 establishes a physical link between E-cadherin and EGFR. Indeed, our results demonstrate that galectin-7 also binds to EGFR, but unlike the binding to E-cadherin this binding is sugar dependent. The establishment of E-cadherin/EGFR complex and the binding of galectin-7 to EGFR thus lead to a regulation of its signaling and intracellular trafficking allowing cell proliferation and migration control. In vivo observations further support these results since an epidermal thickening is observed in galectin-7 deficient mice. This study therefore reveals that galectin-7 controls epidermal homeostasis through the regulation of E-cadherin/EGFR balance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism*
  • Cadherins / metabolism*
  • Cell Differentiation / genetics
  • Cell Membrane / metabolism
  • Cell Movement / genetics
  • Cell Proliferation / genetics
  • Epidermis / metabolism
  • ErbB Receptors / metabolism*
  • Female
  • Galectins / genetics
  • Galectins / metabolism
  • Gene Silencing
  • HaCaT Cells
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Molecular Docking Simulation
  • Signal Transduction / genetics*

Substances

  • Antigens, CD
  • CDH1 protein, human
  • Cadherins
  • Cdh1 protein, mouse
  • Galectins
  • LGALS7 protein, human
  • Lgals7 protein, mouse
  • EGFR protein, human
  • EGFR protein, mouse
  • ErbB Receptors