The Research Center and Department of Pathology, Zhongshan Hospital of Dalian University, Dalian 116001, China.
Department of Orofacial Sciences and Program in Craniofacial Biology, University of California, San Francisco, California 94143, USA.
Nat Commun. 2016 Jul 13;7:12133. doi: 10.1038/ncomms12133.
Embryonic signalling centres are specialized clusters of non-proliferating cells that direct the development of many organs. However, the mechanisms that establish these essential structures in mammals are not well understood. Here we report, using the murine incisor as a model, that αE-catenin is essential for inhibiting nuclear YAP localization and cell proliferation. This function of αE-catenin is required for formation of the tooth signalling centre, the enamel knot (EK), which maintains dental mesenchymal condensation and epithelial invagination. EK formation depends primarily on the signalling function of αE-catenin through YAP and its homologue TAZ, as opposed to its adhesive function, and combined deletion of Yap and Taz rescues the EK defects caused by loss of αE-catenin. These findings point to a developmental mechanism by which αE-catenin restricts YAP/TAZ activity to establish a group of non-dividing and specialized cells that constitute a signalling centre.
胚胎信号中心是专门的非增殖细胞簇,可指导许多器官的发育。然而,在哺乳动物中建立这些基本结构的机制尚不清楚。在这里,我们使用鼠门牙作为模型,报道了 αE-连环蛋白对于抑制核 YAP 定位和细胞增殖是必需的。αE-连环蛋白的这一功能对于牙齿信号中心——釉结(EK)的形成是必需的,该中心维持牙间充质的凝聚和上皮内陷。EK 的形成主要取决于 αE-连环蛋白通过 YAP 和其同源物 TAZ 的信号功能,而不是其黏附功能,并且 Yap 和 Taz 的联合缺失可挽救因 αE-连环蛋白缺失而引起的 EK 缺陷。这些发现指出了一种发育机制,通过该机制,αE-连环蛋白限制 YAP/TAZ 的活性,以建立一群非分裂和专门的细胞,构成一个信号中心。