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从二维图像堆叠中重建三维组织学体积的变换扩散。

Transformation diffusion reconstruction of three-dimensional histology volumes from two-dimensional image stacks.

机构信息

Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford OX3 7DQ, UK.

Heart Science Centre, National Lung and Heart Institute, Imperial College London, Harefield UB9 6JH, UK.

出版信息

Med Image Anal. 2017 May;38:184-204. doi: 10.1016/j.media.2017.03.004. Epub 2017 Mar 23.

Abstract

Traditional histology is the gold standard for tissue studies, but it is intrinsically reliant on two-dimensional (2D) images. Study of volumetric tissue samples such as whole hearts produces a stack of misaligned and distorted 2D images that need to be reconstructed to recover a congruent volume with the original sample's shape. In this paper, we develop a mathematical framework called Transformation Diffusion (TD) for stack alignment refinement as a solution to the heat diffusion equation. This general framework does not require contour segmentation, is independent of the registration method used, and is trivially parallelizable. After the first stack sweep, we also replace registration operations by operations in the space of transformations, several orders of magnitude faster and less memory-consuming. Implementing TD with operations in the space of transformations produces our Transformation Diffusion Reconstruction (TDR) algorithm, applicable to general transformations that are closed under inversion and composition. In particular, we provide formulas for translation and affine transformations. We also propose an Approximated TDR (ATDR) algorithm that extends the same principles to tensor-product B-spline transformations. Using TDR and ATDR, we reconstruct a full mouse heart at pixel size 0.92µm×0.92µm, cut 10µm thick, spaced 20µm (84G). Our algorithms employ only local information from transformations between neighboring slices, but the TD framework allows theoretical analysis of the refinement as applying a global Gaussian low-pass filter to the unknown stack misalignments. We also show that reconstruction without an external reference produces large shape artifacts in a cardiac specimen while still optimizing slice-to-slice alignment. To overcome this problem, we use a pre-cutting blockface imaging process previously developed by our group that takes advantage of Brewster's angle and a polarizer to capture the outline of only the topmost layer of wax in the block containing embedded tissue for histological sectioning.

摘要

传统的组织学是组织研究的金标准,但它本质上依赖于二维(2D)图像。对整个心脏等体积组织样本的研究产生了一系列未对准和变形的 2D 图像,需要对其进行重建,以恢复与原始样本形状一致的体积。在本文中,我们开发了一种称为变换扩散(TD)的数学框架,作为热扩散方程的解决方案,用于堆栈对准细化。这个通用框架不需要轮廓分割,独立于使用的配准方法,并且可以轻松地进行并行化。在第一次堆栈扫描之后,我们还通过变换空间中的操作替换配准操作,速度快几个数量级,消耗的内存少。通过在变换空间中进行操作来实现 TD 会产生我们的变换扩散重建(TDR)算法,适用于在反转和组合下封闭的一般变换。特别是,我们提供了平移和仿射变换的公式。我们还提出了一种近似 TDR(ATDR)算法,该算法将相同的原理扩展到张量积 B 样条变换。使用 TDR 和 ATDR,我们以 0.92µm×0.92µm 的像素大小重建完整的老鼠心脏,厚度为 10µm,间隔 20µm(84G)。我们的算法仅使用相邻切片之间变换的局部信息,但 TD 框架允许对细化进行理论分析,即将全局高斯低通滤波器应用于未知的堆栈未对准。我们还表明,在没有外部参考的情况下进行重建会在心脏标本中产生大的形状伪影,同时仍优化切片到切片的对准。为了克服这个问题,我们使用了我们小组先前开发的预切割块面成像过程,该过程利用布鲁斯特角和偏光器仅捕获块中嵌入组织的蜡的最顶层的轮廓,用于组织学切片。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63ab/5408912/a62a5baf4d4f/fx1.jpg

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