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Segmentation of Vascular Structures and Hematopoietic Cells in 3-D Microscopy Images and Quantitative Analysis

机译:3-D显微镜图像中血管结构和造血细胞的分割及定量分析

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摘要

In this paper, we present image processing methods for quantitative study of how the bone marrow microenvironment changes (characterized by altered vascular structure and hematopoietic cell distribution) caused by diseases or various factors. We develop algorithms that automatically segment vascular structures and hematopoietic cells in 3-D microscopy images, perform quantitative analysis of the properties of the segmented vascular structures and cells, and examine how such properties change. In processing images, we apply local thresholding to segment vessels, and add post-processing steps to deal with imaging artifacts. We propose an improved watershed algorithm that relies on both intensity and shape information and can separate multiple overlapping cells better than common watershed methods. We then quantitatively compute various features of the vascular structures and hematopoietic cells, such as the branches and sizes of vessels and the distribution of cells. In analyzing vascular properties, we provide algorithms for pruning fake vessel segments and branches based on vessel skeletons. Our algorithms can segment vascular structures and hematopoietic cells with good quality. We use our methods to quantitatively examine the changes in the bone marrow microenvironment caused by the deletion of Notch pathway. Our quantitative analysis reveals property changes in samples with deleted Notch pathway. Our tool is useful for biologists to quantitatively measure changes in the bone marrow microenvironment, for developing possible therapeutic strategies to help the bone marrow microenvironment recovery.
机译:在本文中,我们提出了图像处理方法,用于定量研究由疾病或各种因素引起的骨髓微环境变化(以血管结构改变和造血细胞分布为特征)。我们开发了可在3-D显微镜图像中自动分割血管结构和造血细胞的算法,对分割的血管结构和细胞的性质进行定量分析,并检查这些性质如何变化。在处理图像时,我们将局部阈值应用于分割血管,并添加后处理步骤以处理成像伪像。我们提出了一种改进的分水岭算法,该算法同时依赖于强度和形状信息,并且可以比普通分水岭方法更好地分离多个重叠的像元。然后,我们定量计算血管结构和造血细胞的各种特征,例如血管的分支和大小以及细胞的分布。在分析血管特性时,我们提供了基于血管骨架修剪假血管段和分支的算法。我们的算法可以很好地分割血管结构和造血细胞。我们使用我们的方法来定量检查由Notch通路的缺失引起的骨髓微环境的变化。我们的定量分析揭示了缺口通道缺失的样品的性质变化。我们的工具可帮助生物学家定量测量骨髓微环境的变化,开发可能的治疗策略来帮助骨髓微环境恢复。

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