Molecular Biology and Biochemistry Department, Simon Fraser University, 8888 University Drive, Burnaby, British Columbia, Canada V5A 1S6.
Mech Dev. 2011 Jan-Feb;128(1-2):71-89. doi: 10.1016/j.mod.2010.11.001. Epub 2010 Nov 5.
Glycosaminoglycans (GAGs) are a heavily sulfated component of the extracellular matrix (ECM) implicated in a variety of cell signaling events involved in patterning of embryos. Embryos of the sea urchin Strongylocentrotus purpuratus were exposed to several inhibitors that disrupt GAG function during development. Treatment with chlorate, a general inhibitor of sulfation that leads to undersulfated GAGs, reduced sulfation of the urchin blastocoelar ECM. It also prevented correct specification of the oral-aboral axis and mouth formation, resulting in a radialized phenotype characterized by the lack of an oral field, incomplete gastrulation and formation of multiple skeletal spicule rudiments. Oral markers were initially expressed in most of the prospective ectoderm of chlorate-treated early blastulae, but then declined as aboral markers became expressed throughout most of the ectoderm. Nodal expression in the presumptive oral field is necessary and sufficient to specify the oral-aboral axis in urchins. Several lines of evidence suggest a deregulation of Nodal signaling is involved in the radialization caused by chlorate: (1) Radial embryos resemble those in which Nodal expression was knocked down. (2) Chlorate disrupted localized nodal expression in oral ectoderm, even when applied after the oral-aboral axis is specified and expression of other oral markers is resistant to treatment. (3) Inhibition with SB-431542 of ALK-4/5/7 receptors that mediate Nodal signaling causes defects in ectodermal patterning similar to those caused by chlorate. (4) Intriguingly, treatment of embryos with a sub-threshold dose of SB-431542 rescued the radialization caused by low concentrations of chlorate. Our results indicate important roles for sulfated GAGs in Nodal signaling and oral-aboral axial patterning, and in the cellular processes necessary for archenteron extension and mouth formation during gastrulation. We propose that interaction of the Nodal ligand with sulfated GAGs limits its diffusion, and is required to specify an oral field in the urchin embryo and organize the oral-aboral axis.
糖胺聚糖(GAGs)是细胞外基质(ECM)中高度硫酸化的成分,参与胚胎形态发生的多种细胞信号事件。棘皮动物海胆 Strongylocentrotus purpuratus 的胚胎在发育过程中暴露于几种破坏 GAG 功能的抑制剂中。用氯酸盐处理,一种普遍的硫酸化抑制剂,导致 GAG 硫酸化不足,降低了海胆囊胚腔 ECM 的硫酸化程度。它还阻止了口腔 - 肛门轴和口的正确特化,导致放射状表型,其特征是缺乏口腔场,不完全原肠胚形成和多个骨骼刺突原基的形成。口腔标记物最初在氯酸盐处理的早期囊胚中的大部分预期外胚层中表达,但随后随着肛门口标记物在大部分外胚层中表达而下降。在假定的口腔场中的 Nodal 表达对于指定海胆的口腔 - 肛门轴是必要且充分的。有几条证据表明,氯酸盐引起的放射状化涉及 Nodal 信号的失调:(1)放射状胚胎类似于 Nodal 表达被敲低的胚胎。(2)氯酸盐破坏了口腔外胚层中的局部节点表达,即使在口腔 - 肛门轴被指定并且其他口腔标记物的表达对处理有抗性时也是如此。(3)ALK-4/5/7 受体的 SB-431542 抑制,该受体介导 Nodal 信号传导,导致与氯酸盐引起的缺陷类似的外胚层模式形成缺陷。(4)有趣的是,用低于阈值剂量的 SB-431542 处理胚胎可挽救低浓度氯酸盐引起的放射状化。我们的结果表明,硫酸化 GAGs 在 Nodal 信号传导和口腔 - 肛门轴向模式形成以及在原肠胚形成期间口形成所需的细胞过程中起重要作用。我们提出,Nodal 配体与硫酸化 GAGs 的相互作用限制了其扩散,并需要在海胆胚胎中指定口腔场并组织口腔 - 肛门轴。