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Automatic Detection of Endothelial Cells in 3D Angiogenic Sprouts from Experimental Phase Contrast Images

机译:从实验相衬图像自动检测3D血管新生芽中的内皮细胞

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Cell migration studies in 3D environments become more popular, as cell behaviors in 3D are more similar to the behaviors of cells in a living organism (in vivo). We focus on the 3D angiogenic sprouting in microfluidic devices, where Endothelial Cells (ECs) burrow into the gel matrix and form solid lumen vessels. Phase contrast microscopy is used for long-term observation of the unlabeled ECs in the 3D microfluidic devices. Two template matching based approaches are proposed to automatically detect the unlabeled ECs in the angiogenic sprouts from the acquired experimental phase contrast images. Cell and non-cell templates are obtained from these phase contrast images as the training data. The first approach applies Partial Least Square Regression (PLSR) to find the discriminative features and their corresponding weight to distinguish cells and non-cells, whereas the second approach relies on Principal Component Analysis (PCA) to reduce the template feature dimension and Support Vector Machine (SVM) to find their corresponding weight. Through a sliding window manner, the cells in the test images are detected. We then validate the detection accuracy by comparing the results with the same images acquired with a confocal microscope after cells are fixed and their nuclei are stained. More accurate numerical results are obtained for approach Ⅰ (PLSR) compared to approach Ⅱ (PCA & SVM) for cell detection. Automatic cell detection will aid in the understanding of cell migration in 3D environment and in turn result in a better understanding of angiogenesis.
机译:3D环境中的细胞迁移研究变得越来越普遍,因为3D中的细胞行为与活生物体(体内)中的细胞行为更加相似。我们专注于微流体装置中的3D血管新生,其中内皮细胞(EC)进入凝胶基质并形成固体管腔血管。相衬显微镜用于对3D微流体设备中未标记的EC进行长期观察。提出了两种基于模板匹配的方法,用于从采集的实验相衬图像中自动检测血管生成芽中未标记的EC。从这些相衬图像获得细胞和非细胞模板作为训练数据。第一种方法应用偏最小二乘回归(PLSR)查找判别特征及其相应权重以区分单元格和非单元格,而第二种方法则依靠主成分分析(PCA)来减少模板特征维和支持向量机(SVM)查找它们相应的权重。通过滑动窗口的方式,检测测试图像中的细胞。然后,我们通过将结果与固定细胞并对其细胞核染色后用共聚焦显微镜获得的相同图像进行比较,从而验证检测的准确性。与方法Ⅱ(PCA和SVM)相比,方法Ⅰ(PLSR)获得了更准确的数值结果。自动细胞检测将有助于理解3D环境中的细胞迁移,进而有助于更好地了解血管生成。

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