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非洲爪蟾胚胎中,近轴中胚层对神经嵴的诱导需要成纤维细胞生长因子(FGF)信号。

Neural crest induction by paraxial mesoderm in Xenopus embryos requires FGF signals.

作者信息

Monsoro-Burq Anne-Hélène, Fletcher Russell B, Harland Richard M

机构信息

Department of Molecular and Cellular Biology, University of California at Berkeley, CA 94720, USA.

出版信息

Development. 2003 Jul;130(14):3111-24. doi: 10.1242/dev.00531.

Abstract

At the border of the neural plate, the induction of the neural crest can be achieved by interactions with the epidermis, or with the underlying mesoderm. Wnt signals are required for the inducing activity of the epidermis in chick and amphibian embryos. Here, we analyze the molecular mechanisms of neural crest induction by the mesoderm in Xenopus embryos. Using a recombination assay, we show that prospective paraxial mesoderm induces a panel of neural crest markers (Slug, FoxD3, Zic5 and Sox9), whereas the future axial mesoderm only induces a subset of these genes. This induction is blocked by a dominant negative (dn) form of FGFR1. However, neither dnFGFR4a nor inhibition of Wnt signaling prevents neural crest induction in this system. Among the FGFs, FGF8 is strongly expressed by the paraxial mesoderm. FGF8 is sufficient to induce the neural crest markers FoxD3, Sox9 and Zic5 transiently in the animal cap assay. In vivo, FGF8 injections also expand the Slug expression domain. This suggests that FGF8 can initiate neural crest formation and cooperates with other DLMZ-derived factors to maintain and complete neural crest induction. In contrast to Wnts, eFGF or bFGF, FGF8 elicits neural crest induction in the absence of mesoderm induction and without a requirement for BMP antagonists. In vivo, it is difficult to dissociate the roles of FGF and WNT factors in mesoderm induction and neural patterning. We show that, in most cases, effects on neural crest formation were parallel to altered mesoderm or neural development. However, neural and neural crest patterning can be dissociated experimentally using different dominant-negative manipulations: while Nfz8 blocks both posterior neural plate formation and neural crest formation, dnFGFR4a blocks neural patterning without blocking neural crest formation. These results suggest that different signal transduction mechanisms may be used in neural crest induction, and anteroposterior neural patterning.

摘要

在神经板的边缘,神经嵴的诱导可通过与表皮或其下方的中胚层相互作用来实现。在鸡和两栖类胚胎中,Wnt信号对于表皮的诱导活性是必需的。在此,我们分析了非洲爪蟾胚胎中中胚层诱导神经嵴的分子机制。通过重组实验,我们发现预期的轴旁中胚层可诱导一组神经嵴标记物(Slug、FoxD3、Zic5和Sox9),而未来的轴中胚层仅诱导这些基因的一个子集。这种诱导被FGFR1的显性负性(dn)形式所阻断。然而,dnFGFR4a或Wnt信号的抑制均不能阻止该系统中的神经嵴诱导。在成纤维细胞生长因子(FGFs)中,FGF8在轴旁中胚层中强烈表达。在动物帽实验中,FGF8足以瞬时诱导神经嵴标记物FoxD3、Sox9和Zic5。在体内,注射FGF8也会扩大Slug的表达域。这表明FGF8可启动神经嵴形成,并与其他背侧外侧中胚层(DLMZ)来源的因子协同作用以维持和完成神经嵴诱导。与Wnt、表皮生长因子(eFGF)或碱性成纤维细胞生长因子(bFGF)不同,FGF8在不存在中胚层诱导且无需骨形态发生蛋白(BMP)拮抗剂的情况下即可引发神经嵴诱导。在体内,很难区分FGF和WNT因子在中胚层诱导和神经模式形成中的作用。我们表明,在大多数情况下,对神经嵴形成的影响与中胚层或神经发育的改变平行。然而,使用不同的显性负性操作可通过实验分离神经和神经嵴模式形成:虽然Nfz8可同时阻断后神经板形成和神经嵴形成,但dnFGFR4a可阻断神经模式形成而不阻断神经嵴形成。这些结果表明,在神经嵴诱导和前后神经模式形成中可能使用了不同的信号转导机制。

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