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Embryonic nodal flow and the dynamics of nodal vesicular parcels

机译:胚胎淋巴结流和淋巴结囊泡动力学

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摘要

We address with fluid-dynamical simulations using direct numerical techniques three important and fundamental questions with respect to fluid flow within the mouse node and left–right development. First, we consider the differences between what is experimentally observed when assessing cilium-induced fluid flow in the mouse node in vitro and what is to be expected in vivo. The distinction is that in vivo, the leftward fluid flow across the mouse node takes place within a closed system and is consequently confined, while this is no longer the case on removing the covering membrane and immersing the embryo in a fluid-filled volume to perform in vitro experiments. Although there is a central leftward flow in both instances, we elucidate some important distinctions about the closed in vivo situation. Second, we model the movement of the newly discovered nodal vesicular parcels (NVPs) across the node and demonstrate that the flow should indeed cause them to accumulate on the left side of the node, as required for symmetry breaking. Third, we discuss the rupture of NVPs. Based on the biophysical properties of these vesicles, we argue that the morphogens they contain are likely not delivered to the surrounding cells by their mechanical rupture either by the cilia or the flow, and rupture must instead be induced by an as yet undiscovered biochemical mechanism.
机译:我们使用直接数值技术通过流体动力学模拟解决了关于鼠标节点内的流体流动和左右发展的三个重要且基本的问题。首先,我们考虑了在体外评估纤毛诱导的小鼠淋巴结内的流体流动与体内预期的实验之间的差异。区别在于,在体内,穿过鼠标节点的向左流体流发生在一个封闭的系统内,因此受到限制,而在移除覆盖膜并将胚胎浸入充满流体的体积中以进行操作时,情况不再如此。体外实验。尽管两种情况都有中央向左流动,但我们阐明了封闭体内情况的一些重要区别。其次,我们对新发现的节点水泡小囊(NVP)在整个节点上的运动进行建模,并证明流动确实会导致它们在节点的左侧积聚,这是对称破坏所必需的。第三,我们讨论NVP的破裂。基于这些囊泡的生物物理特性,我们认为它们所包含的形态发生因子可能不会通过纤毛或血流的机械破裂而传递至周围细胞,而破裂必须由尚未发现的生化机制引起。

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