Heid Paul J, Voss Edward, Soll David R
W. M. Keck Dynamic Image Analysis Facility, University of Iowa, Iowa City, Iowa 52242, USA.
Dev Biol. 2002 May 15;245(2):329-47. doi: 10.1006/dbio.2002.0631.
A computer-assisted three-dimensional (3D) system, 3D-DIASemb, has been developed that allows reconstruction and motion analysis of cells and nuclei in a developing embryo. In the system, 75 optical sections through a live embryo are collected in the z axis by using differential interference contrast microscopy. Optical sections for one reconstruction are collected in a 2.5-s period, and this process is repeated every 5 s. The outer perimeter and nuclear perimeter of each cell in the embryo are outlined in each optical section, converted into beta-spline models, and then used to construct 3D faceted images of the surface and nucleus of every cell in the developing embryo. Because all individual components of the embryo (i.e., each cell surface and each nuclear surface) are individually reconstructed, 3D-DIASemb allows isolation and analysis of (1) all or select nuclei in the absence of cell surfaces, (2) any single cell lineage, and (3) any single nuclear lineage through embryogenesis. Because all reconstructions represent mathematical models, 3D-DIASemb computes over 100 motility and dynamic morphology parameters for every cell, nucleus, or group of cells in the developing embryo at time intervals as short as 5 s. Finally, 3D-DIASemb reconstructs and motion analyzes cytoplasmic flow through the generation and analysis of "vector flow plots." To demonstrate the unique capabilities of this new technology, a Caenorhabditis elegans embryo is reconstructed and motion analyzed through the 28-cell stage. Although 3D-DIASemb was developed by using the C. elegans embryo as the experimental model, it can be applied to other embryonic systems. 3D-DIASemb therefore provides a new method for reconstructing and motion analyzing in 4D every cell and nucleus in a live, developing embryo, and should provide a powerful tool for assessing the effects of drugs, environmental perturbations, and mutations on the cellular and nuclear dynamics accompanying embryogenesis.
已开发出一种计算机辅助三维(3D)系统,即3D-DIASemb,它能够对发育中的胚胎中的细胞和细胞核进行重建及运动分析。在该系统中,通过微分干涉对比显微镜在z轴上采集75个穿过活胚胎的光学切片。用于一次重建的光学切片在2.5秒内采集完成,且此过程每5秒重复一次。胚胎中每个细胞的外周和细胞核周长在每个光学切片中勾勒出来,转换为贝塔样条模型,然后用于构建发育中胚胎每个细胞的表面和细胞核的3D多面图像。由于胚胎的所有单个组件(即每个细胞表面和每个细胞核表面)都单独重建,3D-DIASemb允许在没有细胞表面的情况下分离和分析(1)所有或选定的细胞核,(2)任何单个细胞谱系,以及(3)胚胎发生过程中的任何单个核谱系。由于所有重建都代表数学模型,3D-DIASemb能在短至5秒的时间间隔内为发育中胚胎的每个细胞、细胞核或细胞群计算出100多个运动性和动态形态学参数。最后,3D-DIASemb通过生成和分析“矢量流图”来重建和运动分析细胞质流动。为了证明这项新技术的独特能力,对秀丽隐杆线虫胚胎进行了重建,并分析了其到28细胞阶段的运动情况。尽管3D-DIASemb是使用秀丽隐杆线虫胚胎作为实验模型开发的,但它可应用于其他胚胎系统。因此,3D-DIASemb为实时发育胚胎中每个细胞和细胞核的4D重建及运动分析提供了一种新方法,并且应该为评估药物、环境干扰和突变对胚胎发生过程中细胞和核动力学的影响提供一个强大的工具。