Dynamics and functions of E-cadherin complexes in epithelial cell and tissue morphogenesis

被引:3
|
作者
Zhang, Na [1 ]
Haering, Matthias [2 ]
Wolf, Fred [2 ]
Grosshans, Joerg [1 ,2 ]
Kong, Deqing [1 ,2 ]
机构
[1] Philipps Univ, Dept Biol, D-35043 Marburg, Germany
[2] Georg August Univ Gottingen, Inst Dynam Biol Networks CIDBN, Gottingen Campus, D-37073 Gottingen, Germany
关键词
Nanoscale architectures; Phosphorylation; Glycosylation; Computational modelling; DROSOPHILA E-CADHERIN; N-GLYCOSYLATION AFFECTS; ADHERENS JUNCTION; ALPHA-CATENIN; BETA-CATENIN; ENDOPLASMIC-RETICULUM; LIVE-CELL; IN-VITRO; ADHESION; BINDING;
D O I
10.1007/s42995-023-00206-w
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
Cell-cell adhesion is at the center of structure and dynamics of epithelial tissue. E-cadherin-catenin complexes mediate Ca2+-dependent trans-homodimerization and constitute the kernel of adherens junctions. Beyond the basic function of cell-cell adhesion, recent progress sheds light the dynamics and interwind interactions of individual E-cadherin-catenin complex with E-cadherin superclusters, contractile actomyosin and mechanics of the cortex and adhesion. The nanoscale architecture of E-cadherin complexes together with cis-interactions and interactions with cortical actomyosin adjust to junctional tension and mechano-transduction by reinforcement or weakening of specific features of the interactions. Although post-translational modifications such as phosphorylation and glycosylation have been implicated, their role for specific aspects of in E-cadherin function has remained unclear. Here, we provide an overview of the E-cadherin complex in epithelial cell and tissue morphogenesis focusing on nanoscale architectures by super-resolution approaches and post-translational modifications from recent, in particular in vivo, studies. Furthermore, we review the computational modelling in E-cadherin complexes and highlight how computational modelling has contributed to a deeper understanding of the E-cadherin complexes.
引用
收藏
页码:585 / 601
页数:17
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