Perez-Moreno Mirna, Fuchs Elaine
Howard Hughes Medical Institute, Laboratory of Mammalian Cell Biology and Development, The Rockefeller University, New York, New York 10021, USA.
Dev Cell. 2006 Nov;11(5):601-12. doi: 10.1016/j.devcel.2006.10.010.
Adherens junctions have been traditionally viewed as building blocks of tissue architecture. The foundations for this view began to change with the discovery that a central component of AJs, beta-catenin, can also function as a transcriptional cofactor in Wnt signaling. In recent years, conventional views have similarly been shaken about the other two major AJ catenins, alpha-catenin and p120-catenin. Catenins have emerged as molecular sensors that integrate cell-cell junctions and cytoskeletal dynamics with signaling pathways that govern morphogenesis, tissue homeostasis, and even intercellular communication between different cell types within a tissue. These findings reveal novel aspects of AJ function in normal tissues and offer insights into how changes in AJs and their associated proteins and cytoskeletal dynamics impact wound-repair and cancer.
传统上,黏着连接被视为组织结构的基本组成部分。随着发现AJs的核心成分β-连环蛋白也可作为Wnt信号通路中的转录辅因子,这种观点的基础开始发生变化。近年来,关于另外两种主要的AJ连环蛋白α-连环蛋白和p120-连环蛋白的传统观点同样受到了冲击。连环蛋白已成为分子传感器,将细胞间连接和细胞骨架动力学与控制形态发生、组织稳态甚至组织内不同细胞类型之间细胞间通讯的信号通路整合在一起。这些发现揭示了AJs在正常组织中的新功能,并为AJs及其相关蛋白和细胞骨架动力学的变化如何影响伤口修复和癌症提供了见解。