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胚胎期节点流与节点囊泡体的动力学

Embryonic nodal flow and the dynamics of nodal vesicular parcels.

作者信息

Cartwright Julyan H E, Piro Nicolas, Piro Oreste, Tuval Idan

机构信息

Laboratorio de Estudios Cristalográficos, CSIC, 18100 Armilla, Granada, Spain.

出版信息

J R Soc Interface. 2007 Feb 22;4(12):49-55. doi: 10.1098/rsif.2006.0155.

Abstract

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.

摘要

我们运用直接数值技术进行流体动力学模拟,探讨了关于小鼠节点内流体流动和左右发育的三个重要且基本的问题。第一,我们考量了在体外评估小鼠节点中纤毛诱导的流体流动时的实验观测结果与体内预期情况之间的差异。区别在于,在体内,穿过小鼠节点的向左流体流动发生在一个封闭系统中,因此受到限制,而在移除覆盖膜并将胚胎浸入充满液体的容器中进行体外实验时,情况则并非如此。尽管在这两种情况下都存在中央向左流动,但我们阐明了关于体内封闭情况的一些重要区别。第二,我们对新发现的节点囊泡小体(NVPs)穿过节点的运动进行建模,并证明这种流动确实应使它们如对称性破缺所需那样在节点左侧积累。第三,我们讨论了NVPs的破裂。基于这些囊泡的生物物理特性,我们认为它们所含的形态发生素不太可能通过纤毛或流动导致的机械破裂传递给周围细胞,相反,破裂必定是由一种尚未被发现的生化机制诱导的。

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