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Adaptive Geometric Tessellation for 3D Reconstruction of Anisotropically Developing Cells in Multilayer Tissues from Sparse Volumetric Microscopy Images

机译:稀疏体积显微镜图像对多层组织中各向异性发育细胞的3D重建的自适应几何镶嵌。

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摘要

The need for quantification of cell growth patterns in a multilayer, multi-cellular tissue necessitates the development of a 3D reconstruction technique that can estimate 3D shapes and sizes of individual cells from Confocal Microscopy (CLSM) image slices. However, the current methods of 3D reconstruction using CLSM imaging require large number of image slices per cell. But, in case of Live Cell Imaging of an actively developing tissue, large depth resolution is not feasible in order to avoid damage to cells from prolonged exposure to laser radiation. In the present work, we have proposed an anisotropic Voronoi tessellation based 3D reconstruction framework for a tightly packed multilayer tissue with extreme z-sparsity (2–4 slices/cell) and wide range of cell shapes and sizes. The proposed method, named as the ‘Adaptive Quadratic Voronoi Tessellation’ (AQVT), is capable of handling both the sparsity problem and the non-uniformity in cell shapes by estimating the tessellation parameters for each cell from the sparse data-points on its boundaries. We have tested the proposed 3D reconstruction method on time-lapse CLSM image stacks of the Arabidopsis Shoot Apical Meristem (SAM) and have shown that the AQVT based reconstruction method can correctly estimate the 3D shapes of a large number of SAM cells.
机译:需要对多层,多细胞组织中细胞生长模式进行量化的需求,因此需要开发3D重建技术,该技术可以根据共聚焦显微镜(CLSM)图像切片估计单个细胞的3D形状和大小。然而,当前使用CLSM成像的3D重建方法需要每个细胞大量的图像切片。但是,在活跃发育中的组织进行活细胞成像的情况下,大深度分辨率是不可行的,以避免长时间暴露于激光辐射对细胞造成损害。在目前的工作中,我们提出了一种基于各向异性Voronoi镶嵌的3D重建框架,该框架用于紧密包装的多层组织,其具有极高的z稀疏度(2-4个切片/细胞)并且具有广泛的细胞形状和大小。所提出的方法被称为“自适应二次Voronoi镶嵌”(AQVT),它能够通过从其边界上的稀疏数据点估计每个像元的镶嵌参数来处理稀疏问题和像元形状的不均匀性。我们已经对拟南芥芽顶分生组织(SAM)的延时CLSM图像堆栈测试了建议的3D重建方法,并显示基于AQVT的重建方法可以正确估计大量SAM细胞的3D形状。

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