Crosstalk Between β-CATENIN-Mediated Cell Adhesion and the WNT Signaling Pathway

被引:7
|
作者
Liu, Ding-Xi [1 ]
Hao, Shuang-Li [1 ]
Yang, Wan-Xi [1 ]
机构
[1] Zhejiang Univ, Coll Life Sci, Sperm Lab, 866 Yu Hang Tang Rd, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金;
关键词
beta-CATENIN; adherens junctions; Wnt/beta-CATENIN signaling; transcriptional pool; adhesive pool; EPITHELIAL-MESENCHYMAL TRANSITION; E-CADHERIN; ADHERENS JUNCTIONS; UP-REGULATION; N-CADHERIN; NUCLEAR TRANSLOCATION; AXIS FORMATION; GAMMA-CATENIN; BINDING; PROTEIN;
D O I
10.1089/dna.2022.0424
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell adhesion and stable signaling regulation are fundamental ways of maintaining homeostasis. Among them, the Wnt/beta-CATENIN signaling plays a key role in embryonic development and maintenance of body dynamic homeostasis. At the same time, the key signaling molecule beta-CATENIN in the Wnt signaling can also function as a cytoskeletal linker protein to regulate tissue barriers, cell migration, and morphogenesis. Dysregulation of the balance between Wnt signaling and adherens junctions can lead to disease. How beta-CATENIN maintains the independence of these two functions, or mediates the interaction and balance of these two functions, has been explored and debated for a long time. In this study, we will focus on five aspects of beta-CATENIN chaperone molecules, phosphorylation of beta-CATENIN and related proteins, epithelial mesenchymal transition, beta-CATENIN homolog protein gamma-CATENIN and disease, thus deepening the understanding of the Wnt/beta-CATENIN signaling and the homeostasis between cell adhesion and further addressing related disease problems.
引用
收藏
页码:1 / 13
页数:13
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