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首页> 外文期刊>Annals of Biomedical Engineering: The Journal of the Biomedical Engineering Society >Analyzing Remodeling of Cardiac Tissue: A Comprehensive Approach Based on Confocal Microscopy and 3D Reconstructions
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Analyzing Remodeling of Cardiac Tissue: A Comprehensive Approach Based on Confocal Microscopy and 3D Reconstructions

机译:分析心脏组织的重塑:基于共聚焦显微镜和3D重建的综合方法

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Microstructural characterization of cardiac tissue and its remodeling in disease is a crucial step in many basic research projects. We present a comprehensive approach for three-dimensional characterization of cardiac tissue at the submicrometer scale. We developed a compression-free mounting method as well as labeling and imaging protocols that facilitate acquisition of three-dimensional image stacks with scanning confocal microscopy. We evaluated the approach with normal and infarcted ventricular tissue. We used the acquired image stacks for segmentation, quantitative analysis and visualization of important tissue components. In contrast to conventional mounting, compression-free mounting preserved cell shapes, capillary lumens and extracellular laminas. Furthermore, the new approach and imaging protocols resulted in high signal-to-noise ratios at depths up to 60 A mu m. This allowed extensive analyzes revealing major differences in volume fractions and distribution of cardiomyocytes, blood vessels, fibroblasts, myofibroblasts and extracellular space in control vs. infarct border zone. Our results show that the developed approach yields comprehensive data on microstructure of cardiac tissue and its remodeling in disease. In contrast to other approaches, it allows quantitative assessment of all major tissue components. Furthermore, we suggest that the approach will provide important data for physiological models of cardiac tissue at the submicrometer scale.
机译:在许多基础研究项目中,心脏组织的微结构表征及其在疾病中的重塑是至关重要的一步。我们提出了一种在亚微米尺度上对心脏组织进行三维表征的综合方法。我们开发了一种无压缩的安装方法以及标签和成像协议,可通过扫描共聚焦显微镜方便地采集三维图像堆栈。我们评估了正常和梗死的心室组织的方法。我们使用获取的图像堆栈进行重要组织成分的分割,定量分析和可视化。与常规安装相反,无压缩安装保留了细胞形状,毛细血管腔和细胞外层板。此外,新的方法和成像协议在高达60 Aμm的深度产生了很高的信噪比。这允许进行广泛的分析,揭示对照和梗塞边界区域中心肌细胞,血管,成纤维细胞,成肌纤维细胞和细胞外空间的体积分数和分布存在重大差异。我们的结果表明,开发的方法可得出有关心脏组织的微观结构及其在疾病中重塑的全面数据。与其他方法相比,它可以对所有主要组织成分进行定量评估。此外,我们建议该方法将为亚微米规模的心脏组织生理模型提供重要数据。

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