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

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.

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Publication Details

Journal
Cellular and Molecular Life Sciences
Published
2025-06-22
DOI
https://doi.org/10.1007/s00018-025-05776-9
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Yi Wu, Dongyuan Lü, Qihan Ding, Shouqin Lü et al.
Cellular and Molecular Life Sciences
Cellular Mechanics and Interactions
article

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

Yi Wu, Dongyuan Lü, Qihan Ding, Shouqin Lü, Mian Long, Fan Zhang, Lu Zheng
article en

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.

Cellular and Molecular Life SciencesVol. 82(1)
Shandong University (CN), Institute of Mechanics (BG), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 85%
Cellular Mechanics and Interactions
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