From the Department of Pharmacology, Faculty of Medicine, University of Miyazaki, Miyazaki 889-1692, Japan and.
the Department of Clinical Pharmacology, School of Nursing, Faculty of Medicine, University of Miyazaki, Miyazaki 889-1692, Japan.
J Biol Chem. 2019 Feb 22;294(8):2924-2934. doi: 10.1074/jbc.RA118.005471. Epub 2018 Dec 20.
Neural tube closure requires apical constriction during which contraction of the apical F-actin network forces the cell into a wedged shape, facilitating the folding of the neural plate into a tube. However, how F-actin assembly at the apical surface is regulated in mammalian neurulation remains largely unknown. We report here that formin homology 2 domain-containing 3 (Fhod3), a formin protein that mediates F-actin assembly, is essential for cranial neural tube closure in mouse embryos. We found that Fhod3 is expressed in the lateral neural plate but not in the floor region of the closing neural plate at the hindbrain. Consistently, in Fhod3-null embryos, neural plate bending at the midline occurred normally, but lateral plates seemed floppy and failed to flex dorsomedially. Because the apical accumulation of F-actin and constriction were impaired specifically at the lateral plates in Fhod3-null embryos, we concluded that Fhod3-mediated actin assembly contributes to lateral plate-specific apical constriction to advance closure. Intriguingly, Fhod3 expression at the hindbrain was restricted to neuromeric segments called rhombomeres. The rhombomere-specific accumulation of apical F-actin induced by the rhombomere-restricted expression of Fhod3 was responsible for the outward bulging of rhombomeres involving apical constriction along the anteroposterior axis, as rhombomeric bulging was less prominent in Fhod3-null embryos than in the wild type. Fhod3 thus plays a crucial role in the morphological changes associated with neural tube closure at the hindbrain by mediating apical constriction not only in the mediolateral but also in the anteroposterior direction, thereby contributing to tube closure and rhombomere segmentation, respectively.
神经管闭合需要在顶端进行收缩,在此过程中,顶端 F-肌动蛋白网络的收缩迫使细胞呈楔形,从而促进神经板折叠成管状。然而,哺乳动物神经胚发生中顶端 F-肌动蛋白组装是如何被调节的,在很大程度上仍不清楚。我们在这里报告称,形成素同源物 2 结构域包含 3(Fhod3),一种介导 F-肌动蛋白组装的形成素蛋白,对于小鼠胚胎颅神经管闭合是必不可少的。我们发现 Fhod3 在外侧神经板中表达,但在后脑闭合神经板的底部区域不表达。一致地,在 Fhod3 缺失胚胎中,中线的神经板弯曲正常发生,但侧板似乎松软且未能向背内侧弯曲。由于 Fhod3 缺失胚胎中顶端 F-肌动蛋白的积累和收缩仅在侧板中受到损害,我们得出结论,Fhod3 介导的肌动蛋白组装有助于侧向板特有的顶端收缩以推进闭合。有趣的是,Fhod3 在后脑的表达仅限于称为菱脑节的神经节段。Fhod3 的菱脑节特异性表达引起顶端 F-肌动蛋白的特异性积累,导致菱脑节向外膨出,涉及沿前后轴的顶端收缩,因为 Fhod3 缺失胚胎中的菱脑节膨出不如野生型明显。因此,Fhod3 通过介导不仅在中侧而且在前后方向上的顶端收缩,在与后脑神经管闭合相关的形态变化中发挥关键作用,从而分别有助于管闭合和菱脑节的分割。