Sirbu Ioan Ovidiu, Duester Gregg
OncoDevelopmental Biology Program, Burnham Institute for Medical Research, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
Nat Cell Biol. 2006 Mar;8(3):271-7. doi: 10.1038/ncb1374. Epub 2006 Feb 19.
Somitogenesis requires bilateral rhythmic segmentation of paraxial mesoderm along the antero-posterior axis. The location of somite segmentation depends on opposing signalling gradients of retinoic acid (generated by retinaldehyde dehydrogenase-2; Raldh2) anteriorly and fibroblast growth factor (FGF; generated by Fgf8) posteriorly. Retinoic-acid-deficient embryos exhibit somite left-right asymmetry, but it remains unclear how retinoic acid mediates left-right patterning. Here, we demonstrate that retinoic-acid signalling is uniform across the left-right axis and occurs in node ectoderm but not node mesoderm. In Raldh2(-/-) mouse embryos, ectodermal Fgf8 expression encroaches anteriorly into node ectoderm and neural plate, but its expression in presomitic mesoderm is initially unchanged. The late stages of somitogenesis were rescued in Raldh2(-/-) mouse embryos when the maternal diet was supplemented with retinoic acid until only the 6-somite stage, demonstrating that retinoic acid is only needed during node stages. A retinoic-acid-reporter transgene marking the action of maternal retinoic acid in rescued Raldh2(-/-) embryos revealed that the targets of retinoic-acid signalling during somitogenesis are the node ectoderm and the posterior neural plate, not the presomitic mesoderm. Our findings suggest that antagonism of Fgf8 expression by retinoic acid occurs in the ectoderm and that failure of this mechanism generates excessive FGF8 signalling to adjacent mesoderm, resulting initially in smaller somites and then left-right asymmetry.
体节发生需要沿前后轴对轴旁中胚层进行双侧节律性分割。体节分割的位置取决于视黄酸(由视黄醛脱氢酶-2;Raldh2产生)在前和成纤维细胞生长因子(FGF;由Fgf8产生)在后的相反信号梯度。视黄酸缺乏的胚胎表现出体节左右不对称,但视黄酸如何介导左右模式仍不清楚。在这里,我们证明视黄酸信号在左右轴上是均匀的,并且发生在节点外胚层而不是节点中胚层。在Raldh2(-/-)小鼠胚胎中,外胚层Fgf8表达向前侵入节点外胚层和神经板,但其在体节中胚层的表达最初没有变化。当母体饮食中添加视黄酸直到仅6体节阶段时,Raldh2(-/-)小鼠胚胎的体节发生后期得以挽救,这表明视黄酸仅在节点阶段是必需的。一个视黄酸报告转基因标记了挽救的Raldh2(-/-)胚胎中母体视黄酸的作用,揭示了体节发生过程中视黄酸信号的靶标是节点外胚层和后神经板,而不是体节中胚层。我们的研究结果表明,视黄酸对Fgf8表达的拮抗作用发生在外胚层,并且该机制的失败会导致向相邻中胚层过度的FGF8信号传导,最初导致较小的体节,然后导致左右不对称。