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Shroom3 and planar cell polarity couple apical constriction and convergent extension during neural tube morphogenesis

机译:Shroom3和平面细胞极性耦合神经管形态发生过程中的顶收缩和会聚延伸。

摘要

Neural tube closure is a critical developmental event that provides an extraordinary example of how coordinated cell behavior orchestrates the shaping of a complex tissue during vertebrate embryogenesis. Neural tube closure relies on actomyosin contractility to drive specific cellular behaviors such as apical constriction, tissue bending, and directional cell rearrangements. These complicated processes are facilitated by coordinating the activity of Rho-Kinase (Rock), to regulate cytoskeletal dynamics and actomyosin contractility, and the Planar Cell Polarity (PCP) pathway, which controls polarized cellular reorganization to mediate convergent extension of the tissue. Failure to properly coordinate these processes results in a class of highly prevalent, severely debilitating congenital malformations known as neural tube defects. The work described here investigates the role of Shroom3, a regulator of localized Rock activity, as a direct linker between planar cell polarity and actomyosin contractility to facilitate apical constriction, directional bending, cell topography, and subsequent neural tube morphogenesis. udIn mice, simultaneous depletion of Shroom3 and the planar cell polarity components Vangl2 or Wnt5a results in convergent extension failure and an increased liability to neural tube defects. The Shroom3 and planar cell polarity pathways intersect at Dishevelled, as Dishevelled2 (Dvl2), Shroom3, and Rock co-distribute in cells. Dvl2 and Shroom3 form a physical complex mediated by discrete protein-protein domain interactions. Imaging of the neural plate of E8.5 embryos demonstrates that multiple components of the Shroom3 pathway are planar polarized along mediolateral cell junctions in vivo in a PCP-dependent manner. Finally, Shroom3 mutant embryos exhibit defects in planar cell arrangement during neural tube closure, suggesting a role for Shroom3 activity in convergent extension. These findings support a model in which the Shroom3 and planar cell polarity pathways interact to control convergent extension and polarized bending of the neural plate. The results of this study lend insight into the intricate set of mechanisms that regulate neural tube closure and provide a clear illustration of the complex genetic basis of neural tube defects.ud
机译:神经管闭合是至关重要的发育事件,它提供了一个出色的例子,说明了脊椎动物胚胎发生过程中协调的细胞行为如何协调复杂组织的形成。神经管闭合依赖于肌动球蛋白的收缩力来驱动特定的细胞行为,例如根尖收缩,组织弯曲和定向细胞重排。通过协调Rho激酶(Rock)的活性,调节细胞骨架动力学和肌动球蛋白的收缩性以及控制细胞极化的细胞重组以介导组织的收敛性延伸的Planar Cell Polarity(PCP)途径,可以促进这些复杂的过程。无法正确协调这些过程会导致一类高度流行,严重虚弱的先天性畸形,称为神经管缺陷。这里描述的工作调查了Shroom3(一种局部岩石活性调节剂)的作用,它是平面细胞极性和肌动球蛋白收缩性之间的直接连接子,以促进根尖收缩,定向弯曲,细胞形貌以及随后的神经管形态发生。在小鼠中,同时耗尽Shroom3和平面细胞极性成分Vangl2或Wnt5a会导致收敛性延伸失败,并增加对神经管缺陷的承受力。由于Dishevelled2(Dvl2),Shroom3和Rock共同分布在细胞中,因此Shroom3和平面细胞极性途径在Dishevelled处相交。 Dvl2和Shroom3形成由离散的蛋白质-蛋白质结构域相互作用介导的物理复合物。 E8.5胚胎的神经板的成像表明,Shroom3途径的多个成分在体内以PCP依赖性方式沿中外侧细胞连接平面极化。最后,Shroom3突变体胚胎在神经管闭合过程中在平面细胞排列中表现出缺陷,表明Shroom3活性在收敛性延伸中起作用。这些发现支持了一个模型,其中Shroom3和平面细胞极性途径相互作用,以控制神经板的收敛性延伸和极化弯曲。这项研究的结果有助于深入了解调节神经管闭合的复杂机制,并清楚地说明了神经管缺陷的复杂遗传基础。 ud

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    McGreevy Erica;

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  • 年度 2014
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