E-cadherin negatively regulates hESCs endodermal differentiation under varied substrate stiffnesses

Cell Mol Life Sci. 2025 Jun 23;82(1):245. doi: 10.1007/s00018-025-05776-9.

Abstract

Intercellular adhesion is crucial in regulating stemness maintenance and differentiation initiation of embryonic stem cells (ESCs), which is also cooperated with extracellular mechanical microenvironment. Here an in vitro model was used to elucidate the effects of E-cadherin complexes on definitive endoderm (DE)-directed differentiation of hESCs (H1 cells), when the cells were seeded on polyacrylamide hydrogels with varied stiffnesses. Results indicated that stiff substrate increased the proportion of H1 cells differentiating into DE cells and intercellular E-cadherin expression was reduced with progressive stages at same stiffness, presenting a negative correlation of E-cadherin expression with differentiating progress or substrate stiffness. Blocking E-cadherin enhanced the productivity of differentiated cells and promoted the disassembly of intercellular adhesions by translocating YAP into nuclei, which was positively correlated with GATA6 and CXCR4 expressions in a stiffness-dependent manner. This work provided an insight into understanding the roles of E-cadherin-related intercellular adhesion and substrate stiffness in DE-directed differentiation of hESCs.

Keywords: Definitive endodermal differentiation; E-cadherin; Embryonic stem cells; Substrate stiffness; YAP.

MeSH terms

  • Acrylic Resins / chemistry
  • Antigens, CD
  • Cadherins* / genetics
  • Cadherins* / metabolism
  • Cell Adhesion
  • Cell Differentiation*
  • Endoderm* / cytology
  • Endoderm* / metabolism
  • GATA6 Transcription Factor / genetics
  • GATA6 Transcription Factor / metabolism
  • Human Embryonic Stem Cells* / cytology
  • Human Embryonic Stem Cells* / metabolism
  • Humans
  • Hydrogels / chemistry
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / metabolism
  • Transcription Factors / metabolism
  • YAP-Signaling Proteins

Substances

  • Cadherins
  • Receptors, CXCR4
  • GATA6 Transcription Factor
  • YAP-Signaling Proteins
  • CXCR4 protein, human
  • Hydrogels
  • YAP1 protein, human
  • polyacrylamide
  • Transcription Factors
  • CDH1 protein, human
  • Acrylic Resins
  • Antigens, CD