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Planar cell polarity signalling couples cell division and morphogenesis during neurulation

机译:平面细胞极性信号传导介导细胞分裂和形态发生

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Environmental and genetic aberrations lead to neural tube closure defects (NTDs) in 1 out of every 1,000 births(1). Mouse and frog models for these birth defects have indicated that Van Gogh-like 2 (Vangl2, also known as Strabismus) and other components of planar cell polarity (PCP) signalling might control neurulation by promoting the convergence of neural progenitors to the midline(2-8). Here we show a novel role for PCP signalling during neurulation in zebrafish. We demonstrate that non-canonical Wnt/PCP signalling polarizes neural progenitors along the anteroposterior axis. This polarity is transiently lost during cell division in the neural keel but is re-established as daughter cells reintegrate into the neuroepithelium. Loss of zebrafish Vangl2 ( in trilobite mutants) abolishes the polarization of neural keel cells, disrupts re-intercalation of daughter cells into the neuroepithelium, and results in ectopic neural progenitor accumulations and NTDs. Remarkably, blocking cell division leads to rescue of trilobite neural tube morphogenesis despite persistent defects in convergence and extension. These results reveal a function for PCP signalling in coupling cell division and morphogenesis at neurulation and indicate a previously unrecognized mechanism that might underlie NTDs.
机译:环境和遗传畸变导致每1000例新生儿中就有1例神经管闭合缺陷(NTD)(1)。针对这些先天缺陷的小鼠和青蛙模型表明,梵高样2(Vangl2,也称为斜视)和平面细胞极性(PCP)信号传导的其他成分可能通过促进神经祖细胞向中线的融合来控制神经(2)。 -8)。在这里,我们展示了斑马鱼在神经过程中PCP信号传导的新作用。我们证明,非规范的Wnt / PCP信号会沿前后轴极化神经祖细胞。这种极性在神经龙骨的细胞分裂过程中暂时消失,但是随着子细胞重新整合到神经上皮中而重新建立。斑马鱼Vangl2的丢失(在三叶虫突变体中)消除了神经龙骨细胞的极化,破坏了子细胞重新插入神经上皮细胞,并导致异位神经祖细胞积聚和NTD。值得注意的是,尽管会聚和延伸存在持续性缺陷,但阻断细胞分裂仍可挽救三叶虫神经管的形态发生。这些结果揭示了PCP信号传导在神经细胞耦合分化和形态发生中的功能,并表明可能是NTD潜在的尚未被认识的机制。

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