Gene Regulation Research, Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5 Takayama, Nara 630-0101, Japan.
Proc Natl Acad Sci U S A. 2011 Jun 14;108(24):9881-6. doi: 10.1073/pnas.1017248108. Epub 2011 May 31.
The assembly of progenitor cells is a crucial step for organ formation during vertebrate development. Kupffer's vesicle (KV), a key organ required for the left-right asymmetric body plan in zebrafish, is generated from a cluster of ~20 dorsal forerunner cells (DFCs). Although several genes are known to be involved in KV formation, how DFC clustering is regulated and how cluster formation then contributes to KV formation remain unclear. Here we show that positive feedback regulation of FGF signaling by Canopy1 (Cnpy1) controls DFC clustering. Cnpy1 positively regulates FGF signals within DFCs, which in turn promote Cadherin1-mediated cell adhesion between adjacent DFCs to sustain cell cluster formation. When this FGF positive feedback loop is disrupted, the DFC cluster fails to form, eventually leading to KV malformation and defects in the establishment of laterality. Our results therefore uncover both a previously unidentified role of FGF signaling during vertebrate organogenesis and a regulatory mechanism underlying cell cluster formation, which is an indispensable step for formation of a functional KV and establishment of the left-right asymmetric body plan.
祖细胞的组装是脊椎动物发育过程中器官形成的关键步骤。Kupffer 囊(KV)是斑马鱼左右对称体轴形成所必需的关键器官,由大约 20 个背侧前体细胞(DFC)簇产生。尽管已知有几个基因参与 KV 的形成,但 DFC 簇的调控方式以及簇的形成如何促进 KV 的形成仍不清楚。在这里,我们表明,Canopy1(Cnpy1)对 FGF 信号的正反馈调节控制着 DFC 的聚集。Cnpy1 在 DFC 内正向调节 FGF 信号,而 FGF 信号反过来又促进相邻 DFC 之间 Cadherin1 介导的细胞黏附,以维持细胞簇的形成。当这个 FGF 正反馈环被破坏时,DFC 簇无法形成,最终导致 KV 畸形,并影响左右不对称性的建立。因此,我们的研究结果揭示了 FGF 信号在脊椎动物器官发生过程中的一个以前未被识别的作用,以及细胞簇形成的调节机制,这是形成功能性 KV 和建立左右不对称体轴所必需的步骤。