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鼠 Wnt/PCP 蛋白 Vangl2 对于面部分支运动神经元的迁移是必需的,并且其功能独立于 Dishevelled。

The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of Dishevelled.

机构信息

Division of Biological Sciences, Bond Life Sciences Center, University of Missouri, Columbia, 65211, USA.

出版信息

Dev Biol. 2012 Sep 15;369(2):211-22. doi: 10.1016/j.ydbio.2012.06.021. Epub 2012 Jul 4.

Abstract

During development, facial branchiomotor (FBM) neurons, which innervate muscles in the vertebrate head, migrate caudally and radially within the brainstem to form a motor nucleus at the pial surface. Several components of the Wnt/planar cell polarity (PCP) pathway, including the transmembrane protein Vangl2, regulate caudal migration of FBM neurons in zebrafish, but their roles in neuronal migration in mouse have not been investigated in detail. Therefore, we analyzed FBM neuron migration in mouse looptail (Lp) mutants, in which Vangl2 is inactivated. In Vangl2(Lp/+) and Vangl2(Lp/Lp) embryos, FBM neurons failed to migrate caudally from rhombomere (r) 4 into r6. Although caudal migration was largely blocked, many FBM neurons underwent normal radial migration to the pial surface of the neural tube. In addition, hindbrain patterning and FBM progenitor specification were intact, and FBM neurons did not transfate into other non-migratory neuron types, indicating a specific effect on caudal migration. Since loss-of-function in some zebrafish Wnt/PCP genes does not affect caudal migration of FBM neurons, we tested whether this was also the case in mouse. Embryos null for Ptk7, a regulator of PCP signaling, had severe defects in caudal migration of FBM neurons. However, FBM neurons migrated normally in Dishevelled (Dvl) 1/2 double mutants, and in zebrafish embryos with disrupted Dvl signaling, suggesting that Dvl function is essentially dispensable for FBM neuron caudal migration. Consistent with this, loss of Dvl2 function in Vangl2(Lp/+) embryos did not exacerbate the Vangl2(Lp/+) neuronal migration phenotype. These data indicate that caudal migration of FBM neurons is regulated by multiple components of the Wnt/PCP pathway, but, importantly, may not require Dishevelled function. Interestingly, genetic-interaction experiments suggest that rostral FBM neuron migration, which is normally suppressed, depends upon Dvl function.

摘要

在发育过程中,支配脊椎动物头部肌肉的面脑神经运动(FBM)神经元在脑桥内向尾部和径向迁移,在软脑膜表面形成运动核。Wnt/平面细胞极性(PCP)途径的几个组成部分,包括跨膜蛋白 Vangl2,调节斑马鱼 FBM 神经元的尾部迁移,但它们在小鼠神经元迁移中的作用尚未详细研究。因此,我们分析了 Vangl2 失活的小鼠 looptail(Lp)突变体中的 FBM 神经元迁移。在 Vangl2(+/+)和 Vangl2(Lp/Lp)胚胎中,FBM 神经元未能从菱脑节(r)4向 r6尾部迁移。尽管尾部迁移被大大阻断,但许多 FBM 神经元正常地向神经管的软脑膜表面进行径向迁移。此外,后脑模式和 FBM 祖细胞的指定是完整的,FBM 神经元没有转变成其他非迁移神经元类型,表明对尾部迁移有特异性影响。由于一些斑马鱼 Wnt/PCP 基因的功能丧失不影响 FBM 神经元的尾部迁移,我们测试了这种情况在小鼠中是否也是如此。PCP 信号转导调节剂 Ptk7 的缺失导致 FBM 神经元尾部迁移严重缺陷。然而,在 Dvl 信号转导受损的斑马鱼胚胎中,FBM 神经元正常迁移,并且在 Dvl1/2 双突变体中,FBM 神经元迁移正常,表明 Dvl 功能对于 FBM 神经元尾部迁移基本上是可有可无的。与此一致的是,在 Vangl2(+/+)胚胎中缺失 Dvl2 功能并没有加剧 Vangl2(+/+)神经元迁移表型。这些数据表明,FBM 神经元的尾部迁移受 Wnt/PCP 途径的多个组成部分调节,但重要的是,可能不需要 Dishevelled 功能。有趣的是,遗传相互作用实验表明,正常受抑制的头部 FBM 神经元迁移依赖于 Dvl 功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc4/3484895/c7be0e7dca7b/nihms-396616-f0001.jpg

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