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Sequential Contraction and Exchange of Apical Junctions Drives Zippering and Neural Tube Closure in a Simple Chordate

机译:尖顶连接点的顺序收缩和交换驱动拉链中的拉链和神经管闭合。

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Unidirectional zippering is a key step in neural tube closure that remains poorly understood. Here, we combine experimental and computational approaches to identify the mechanism for zippering in a basal chordate, Ciona intestinalis. We show that myosin II is activated sequentially from posterior to anterior along the neural/epidermal (Ne/Epi) boundary just ahead of the advancing zipper. This promotes rapid shortening of Ne/Epi junctions, driving the zipper forward and drawing the neural folds together. Cell contact rearrangements (Ne/Epi + Ne/Epi -> Ne/Ne + Epi/Epi) just behind the zipper lower tissue resistance to zipper progression by allowing transiently stretched cells to detach and relax toward isodiametric shapes. Computer simulations show that measured differences in junction tension, timing of primary contractions, and delay before cell detachment are sufficient to explain the speed and direction of zipper progression and highlight key advantages of a sequential contraction mechanism for robust efficient zippering.
机译:单向拉链是神经管闭合的关键步骤,目前尚不清楚。在这里,我们结合了实验方法和计算方法,以确定了在基层碳酸盐(Ciona intestinalis)中拉链的机制。我们显示,肌球蛋白II沿着神经/表皮(Ne / Epi)边界从后到前顺序地被激活,就在前进的拉链前面。这促进了Ne / Epi连接的快速缩短,向前推动拉链并将神经褶皱拉在一起。紧靠拉链后面的细胞接触重排(Ne / Epi + Ne / Epi-> Ne / Ne + Epi / Epi)通过允许瞬时拉伸的细胞分离并向等直径形状放松,降低了组织对拉链进展的抵抗力。计算机仿真表明,在连接张力,主收缩时机和细胞脱离之前的延迟中测得的差异足以说明拉链进展的速度和方向,并突出了顺序收缩机制的关键优势,可实现有效的高效拉链。

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