通过基于神经网络模型的斑马鱼胚胎三维有限元模型加速,确定平流在骨形态发生蛋白模式中的作用

Linlin Li, Xu Wang, Junyi Chai, Xiaoqian Wang, Adrián Buganza-Tepole, David M. Umulis
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引用次数: 1

摘要

胚胎发育是一个综合遗传调控和生物力学细胞行为的复杂现象。然而,这些因素对时空形态发生分布的相对影响尚不清楚。骨形态发生蛋白(BMP)是指导早期斑马鱼胚胎背腹侧(DV)模式形成的主要形态发生素,BMP信号传导由细胞外和细胞内因子网络调节,这些因子影响BMP配体的范围和信号传导。在理解模式形成机制方面的最新进展支持源-汇机制,然而,尚不清楚源-汇机构如何在三维(3D)空间中塑造形态发生模式,也不清楚该模式对胚胎前后(AP)和DV轴的生物物理速率和边界条件有多敏感,也不知道如何随时间控制图案。在整个囊胚形成和原肠胚形成过程中,主要的细胞运动,称为脱落,与BMP介导的DV模式一起发生。当上皮细胞向胚胎的植物极扩散时,上皮细胞层开始变薄,直到完全吞噬卵黄细胞。这个动态域可能通过平流影响BMP网络成员的分布。我们开发了一个有限元模型(FEM),该模型结合了斑马鱼胚胎发育的所有阶段的数据,并求解了生长区域中的平流-扩散反应偏微分方程(PDE)。我们使用该模型来研究在脱毛过程中BMP驱动的DV模式的潜在机制。对于参数探索来说,求解PDE在计算上是昂贵的。为了克服这一障碍,我们开发了一种准确快速的3D胚胎神经网络(NN)元模型,并提供了高维输入和输出之间的非线性映射,取代了PDE的直接数值模拟。通过NN元模型的建模和加速,我们确定了平流对模式的影响以及调节因子的动态表达水平对BMP信号网络的影响。
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Determining the role of advection in patterning by bone morphogenetic proteins through neural network model-based acceleration of a 3D finite element model of the zebrafish embryo
Embryonic development is a complex phenomenon that integrates genetic regulation and biomechanical cellular behaviors. However, the relative influence of these factors on spatiotemporal morphogen distributions is not well understood. Bone Morphogenetic Proteins (BMPs) are the primary morphogens guiding the dorsal-ventral (DV) patterning of the early zebrafish embryo, and BMP signaling is regulated by a network of extracellular and intracellular factors that impact the range and signaling of BMP ligands. Recent advances in understanding the mechanism of pattern formation support a source-sink mechanism, however, it is not clear how the source-sink mechanism shapes the morphogen patterns in three-dimensional (3D) space, nor how sensitive the pattern is to biophysical rates and boundary conditions along both the anteroposterior (AP) and DV axes of the embryo, nor how the patterns are controlled over time. Throughout blastulation and gastrulation, major cell movement, known as epiboly, happens along with the BMP-mediated DV patterning. The layer of epithelial cells begins to thin as they spread toward the vegetal pole of the embryo until it has completely engulfed the yolk cell. This dynamic domain may influence the distributions of BMP network members through advection. We developed a Finite Element Model (FEM) that incorporates all stages of zebrafish embryonic development data and solves the advection-diffusion-reaction Partial Differential Equations (PDE) in a growing domain. We use the model to investigate mechanisms in underlying BMP-driven DV patterning during epiboly. Solving the PDE is computationally expensive for parameter exploration. To overcome this obstacle, we developed a Neural Network (NN) metamodel of the 3D embryo that is accurate and fast and provided a nonlinear map between high-dimensional input and output that replaces the direct numerical simulation of the PDEs. From the modeling and acceleration by the NN metamodels, we identified the impact of advection on patterning and the influence of the dynamic expression level of regulators on the BMP signaling network.
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