Carreira-Barbosa Filipa, Kajita Mihoko, Morel Veronique, Wada Hironori, Okamoto Hitoshi, Martinez Arias Alfonso, Fujita Yasuyuki, Wilson Stephen W, Tada Masazumi
Department of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK.
Development. 2009 Feb;136(3):383-92. doi: 10.1242/dev.026542. Epub 2008 Dec 17.
During vertebrate gastrulation, the body axis is established by coordinated and directional movements of cells that include epiboly, involution, and convergence and extension (C&E). Recent work implicates a non-canonical Wnt/planar cell polarity (PCP) pathway in the regulation of C&E. The Drosophila atypical cadherin Flamingo (Fmi) and its vertebrate homologue Celsr, a 7-pass transmembrane protein with extracellular cadherin repeats, regulate several biological processes, including C&E, cochlear cell orientation, axonal pathfinding and neuronal migration. Fmi/Celsr can function together with molecules involved in PCP, such as Frizzled (Fz) and Dishevelled (Dsh), but there is also some evidence that it may act as a cell adhesion molecule in a PCP-pathway-independent manner. We show that abrogation of Celsr activity in zebrafish embryos results in epiboly defects that appear to be independent of the requirement for Celsr in PCP signalling during C&E. Using a C-terminal truncated form of Celsr that inhibits membrane presentation of wild-type Celsr through its putative pro-region, a hanging drop assay reveals that cells from embryos with compromised Celsr activity have different cohesive properties from wild-type cells. It is disruption of this ability of Celsr to affect cell cohesion that primarily leads to the in vivo epiboly defects. In addition, Lyn-Celsr, in which the intracellular domain of Celsr is fused to a membrane localisation signal (Lyn), inhibits Fz-Dsh complex formation during Wnt/PCP signalling without affecting epiboly. Fmi/Celsr therefore has a dual role in mediating two separate morphogenetic movements through its roles in mediating cell cohesion and Wnt/PCP signalling during zebrafish gastrulation.
在脊椎动物原肠胚形成过程中,细胞通过包括外包、内卷以及汇聚延伸(C&E)在内的协调定向运动来建立身体轴。最近的研究表明,非经典Wnt/平面细胞极性(PCP)通路参与了C&E的调控。果蝇非典型钙黏蛋白火烈鸟(Fmi)及其脊椎动物同源物Celsr是一种具有细胞外钙黏蛋白重复序列的7次跨膜蛋白,它调节多种生物学过程,包括C&E、耳蜗细胞定向、轴突导向和神经元迁移。Fmi/Celsr可以与参与PCP的分子如卷曲蛋白(Fz)和散乱蛋白(Dsh)一起发挥作用,但也有一些证据表明它可能以一种不依赖PCP通路的方式作为细胞黏附分子发挥作用。我们发现,斑马鱼胚胎中Celsr活性的缺失会导致外包缺陷,这似乎与Celsr在C&E过程中PCP信号传导中的需求无关。使用Celsr的C端截短形式,通过其假定的前区域抑制野生型Celsr的膜呈现,悬滴试验表明,Celsr活性受损的胚胎细胞与野生型细胞具有不同的黏附特性。正是Celsr影响细胞黏附能力的破坏主要导致了体内外包缺陷。此外,Lyn-Celsr(其中Celsr的细胞内结构域与膜定位信号Lyn融合)在Wnt/PCP信号传导过程中抑制Fz-Dsh复合物的形成,而不影响外包。因此,在斑马鱼原肠胚形成过程中,Fmi/Celsr通过其在介导细胞黏附和Wnt/PCP信号传导中的作用,在介导两种独立的形态发生运动中具有双重作用。