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从稀疏标记细胞的位置数据重建用于弯曲上皮片形态发生的三维变形动力学。

Reconstructing 3D deformation dynamics for curved epithelial sheet morphogenesis from positional data of sparsely-labeled cells.

作者信息

Morishita Yoshihiro, Hironaka Ken-Ichi, Lee Sang-Woo, Jin Takashi, Ohtsuka Daisuke

机构信息

Laboratory for Developmental Morphogeometry, RIKEN Quantitative Biology Center, Kobe, 650-0047, Japan.

Research Fellow of the Japan Society for the Promotion of Science, Tokyo, Japan.

出版信息

Nat Commun. 2017 May 2;8(1):15. doi: 10.1038/s41467-017-00023-7.

Abstract

Quantifying global tissue deformation patterns is essential for understanding how organ-specific morphology is generated during development and regeneration. However, due to imaging difficulties and complex morphology, little is known about deformation dynamics for most vertebrate organs such as the brain and heart. To better understand these dynamics, we propose a method to precisely reconstruct global deformation patterns for three-dimensional morphogenesis of curved epithelial sheets using positional data from labeled cells representing only 1-10% of the entire tissue with limited resolution. By combining differential-geometrical and Bayesian frameworks, the method is applicable to any morphology described with arbitrary coordinates, and ensures the feasibility of analyzing many vertebrate organs. Application to data from chick forebrain morphogenesis demonstrates that our method provides not only a quantitative description of tissue deformation dynamics but also predictions of the mechanisms that determine organ-specific morphology, which could form the basis for the multi-scale understanding of organ morphogenesis.Quantifying deformation patterns of curved epithelial sheets is challenging owing to imaging difficulties. Here the authors develop a method to obtain a quantitative description of 3D tissue deformation dynamics from a small set of cell positional data and applied it to chick forebrain morphogenesis.

摘要

量化全局组织变形模式对于理解器官特异性形态在发育和再生过程中如何形成至关重要。然而,由于成像困难和形态复杂,对于大多数脊椎动物器官(如大脑和心脏)的变形动力学了解甚少。为了更好地理解这些动力学,我们提出了一种方法,利用仅占整个组织1%-10%的标记细胞的位置数据,以有限的分辨率精确重建弯曲上皮片三维形态发生的全局变形模式。通过结合微分几何和贝叶斯框架,该方法适用于用任意坐标描述的任何形态,并确保了分析许多脊椎动物器官的可行性。应用于鸡前脑形态发生的数据表明,我们的方法不仅提供了组织变形动力学的定量描述,还预测了决定器官特异性形态的机制,这可为多尺度理解器官形态发生奠定基础。由于成像困难,量化弯曲上皮片的变形模式具有挑战性。本文作者开发了一种方法,可从一小组细胞位置数据中获得三维组织变形动力学的定量描述,并将其应用于鸡前脑形态发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bb/5432036/c0703e023b94/41467_2017_23_Fig1_HTML.jpg

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