Zhang Zhibin, Lin Xi, Wei Ling, Wu Yiran, Xu Lu, Wu Lijie, Wei Xiaohu, Zhao Suwen, Zhu Xiangjia, Xu Fei
iHuman Institute, ShanghaiTech University, Shanghai, China.
School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Cell Discov. 2024 Jan 5;10(1):3. doi: 10.1038/s41421-023-00627-y.
The ten Frizzled receptors (FZDs) are essential in Wnt signaling and play important roles in embryonic development and tumorigenesis. Among these, FZD6 is closely associated with lens development. Understanding FZD activation mechanism is key to unlock these emerging targets. Here we present the cryo-EM structures of FZD6 and FZD3 which are known to relay non-canonical planar cell polarity (PCP) signaling pathways as well as FZD1 in their G protein-coupled states and in the apo inactive states, respectively. Comparison of the three inactive/active pairs unveiled a shared activation framework among all ten FZDs. Mutagenesis along with imaging and functional analysis on the human lens epithelial tissues suggested potential crosstalk between the G-protein coupling of FZD6 and the PCP signaling pathways. Together, this study provides an integrated understanding of FZD structure and function, and lays the foundation for developing therapeutic modulators to activate or inhibit FZD signaling for a range of disorders including cancers and cataracts.
十种卷曲受体(FZDs)在Wnt信号传导中至关重要,在胚胎发育和肿瘤发生中发挥重要作用。其中,FZD6与晶状体发育密切相关。了解FZD激活机制是解锁这些新兴靶点的关键。在这里,我们展示了FZD6和FZD3的冷冻电镜结构,已知它们分别在其G蛋白偶联状态和无配体失活状态下传递非经典平面细胞极性(PCP)信号通路以及FZD1。对这三对失活/激活状态的比较揭示了所有十种FZDs之间共享的激活框架。对人晶状体上皮组织进行的诱变以及成像和功能分析表明,FZD6的G蛋白偶联与PCP信号通路之间存在潜在的串扰。总之,这项研究提供了对FZD结构和功能的综合理解,并为开发治疗调节剂奠定了基础,以激活或抑制FZD信号传导,用于治疗包括癌症和白内障在内的一系列疾病。