Department of Biomedical Sciences, University of Padua, 35126 Padua, Italy.
Proc Natl Acad Sci U S A. 2012 Sep 18;109(38):15354-9. doi: 10.1073/pnas.1203000109. Epub 2012 Sep 4.
The Spemann organizer stands out from other signaling centers of the embryo because of its broad patterning effects. It defines development along the anteroposterior and dorsoventral axes of the vertebrate body, mainly by secreting antagonists of growth factors. Qualitative models proposed more than a decade ago explain the organizer's region-specific inductions (i.e., head and trunk) as the result of different combinations of antagonists. For example, head induction is mediated by extracellular inhibition of Wnt, BMP, and Nodal ligands. However, little is known about how the levels of these antagonists become harmonized with those of their targets and with the factors initially responsible for germ layers and organizer formation, including Nodal itself. Here we show that key ingredients of the head-organizer development, namely Nodal ligands, Nodal antagonists, and ADMP ligands reciprocally adjust each other's strength and range of activity by a self-regulating network of interlocked feedback and feedforward loops. A key element in this cross-talk is the limited availability of ACVR2a, for which Nodal and ADMP must compete. By trapping Nodal extracellularly, the Nodal antagonists Cerberus and Lefty are permissive for ADMP activity. The system self-regulates because ADMP/ACVR2a/Smad1 signaling in turn represses the expression of the Nodal antagonists, reestablishing the equilibrium. In sum, this work reveals an unprecedented set of interactions operating within the organizer that is critical for embryonic patterning.
Spemann 组织者有别于胚胎中的其他信号中心,因为它具有广泛的模式形成效应。它通过分泌生长因子拮抗剂来定义脊椎动物体的前后轴和背腹轴的发育,主要通过分泌生长因子拮抗剂来定义。十多年前提出的定性模型解释了组织者的区域特异性诱导(即头部和躯干)是不同拮抗剂组合的结果。例如,头部诱导是通过细胞外抑制 Wnt、BMP 和 Nodal 配体来介导的。然而,对于这些拮抗剂的水平如何与它们的靶标以及最初负责 germ layers 和组织者形成的因素(包括 Nodal 本身)协调,我们知之甚少。在这里,我们表明,头部组织者发育的关键成分,即 Nodal 配体、Nodal 拮抗剂和 ADMP 配体,通过相互连锁的反馈和前馈回路的自我调节网络,相互调整彼此的强度和活性范围。这种串扰的一个关键因素是 ACVR2a 的有限可用性,Nodal 和 ADMP 必须为此竞争。通过将 Nodal 细胞外捕获,Nodal 拮抗剂 Cerberus 和 Lefty 允许 ADMP 活性。该系统自我调节,因为 ADMP/ACVR2a/Smad1 信号反过来又抑制了 Nodal 拮抗剂的表达,从而重新建立了平衡。总之,这项工作揭示了一个在组织者内运作的、对胚胎模式形成至关重要的前所未有的相互作用集。