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3D membrane segmentation and quantification of intact thick cells using cryo soft X-ray transmission microscopy : A pilot study

机译:使用低温软X射线透射显微镜对完整厚细胞进行3D膜分割和定量:一项初步研究

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摘要

Structural analysis of biological membranes is important for understanding cell and subcellular organelle function as well as their interaction with the surrounding environment. Imaging of whole cells in three dimension at high spatial resolution remains a significant challenge, particularly for thick cells. Cryo-transmission soft X-ray microscopy (cryo-TXM) has recently gained popularity to image, in 3D, intact thick cells (∼10μm) with details of subcellular architecture and organization in near-native state. This paper reports a new tool to segment and quantify structural changes of biological membranes in 3D from cryo-TXM images by tracking an initial 2D contour along the third axis of the microscope, through a multi-scale ridge detection followed by an active contours-based model, with a subsequent refinement along the other two axes. A quantitative metric that assesses the grayscale profiles perpendicular to the membrane surfaces is introduced and shown to be linearly related to the membrane thickness. Our methodology has been validated on synthetic phantoms using realistic microscope properties and structure dimensions, as well as on real cryo-TXM data. Results demonstrate the validity of our algorithms for cryo-TXM data analysis.
机译:生物膜的结构分析对于理解细胞和亚细胞器的功能及其与周围环境的相互作用非常重要。在高空间分辨率下对全细胞进行三维成像仍然是一项重大挑战,特别是对于厚细胞。低温透射软X射线显微镜(cryo-TXM)最近在3D完整厚细胞(〜10μm)的图像中得到了普及,其亚细胞结构和组织的细节处于接近原始状态。本文报告了一种新工具,该工具可通过沿着显微镜第三轴跟踪初始2D轮廓,通过多尺度脊检测以及随后基于活动轮廓的方法,从冷冻TXM图像中分割和量化3D生物膜在生物膜中的结构变化。模型,然后沿其他两个轴进行细化。引入了一种评估垂直于膜表面的灰度轮廓的定量指标,该定量指标与膜厚度呈线性关系。我们的方法已经通过使用真实的显微镜特性和结构尺寸以及真实的cryo-TXM数据在合成体模上得到了验证。结果证明了我们的算法对cryo-TXM数据分析的有效性。

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