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Eur J Histochem. 2014 Dec 17;58(4):2448. doi: 10.4081/ejh.2014.2448.
2
Whole-body imaging with single-cell resolution by tissue decolorization.组织脱色实现单细胞分辨率的全身成像。
Cell. 2014 Nov 6;159(4):911-24. doi: 10.1016/j.cell.2014.10.034.
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Remodeling of cardiac passive electrical properties and susceptibility to ventricular and atrial arrhythmias.心脏被动电特性重塑以及对室性和房性心律失常的易感性。
Front Physiol. 2014 Nov 3;5:424. doi: 10.3389/fphys.2014.00424. eCollection 2014.
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Whole-brain imaging with single-cell resolution using chemical cocktails and computational analysis.使用化学鸡尾酒和计算分析进行单细胞分辨率的全脑成像。
Cell. 2014 Apr 24;157(3):726-39. doi: 10.1016/j.cell.2014.03.042. Epub 2014 Apr 17.
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Easy performance of 6-color confocal immunofluorescence with 4-laser line microscopes.使用四激光线显微镜轻松进行六色共聚焦免疫荧光检测。
Immunol Lett. 2014 Sep;161(1):1-5. doi: 10.1016/j.imlet.2014.04.003. Epub 2014 Apr 12.
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Fibroblasts in myocardial infarction: a role in inflammation and repair.心肌梗死后的成纤维细胞:在炎症和修复中的作用。
J Mol Cell Cardiol. 2014 May;70:74-82. doi: 10.1016/j.yjmcc.2013.11.015. Epub 2013 Dec 7.
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Identification of nodal tissue in the living heart using rapid scanning fiber-optics confocal microscopy and extracellular fluorophores.利用快速扫描纤维光学共聚焦显微镜和细胞外荧光染料识别活体心脏中的节段组织。
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分析心脏组织重塑:基于共聚焦显微镜和三维重建的综合方法。

Analyzing Remodeling of Cardiac Tissue: A Comprehensive Approach Based on Confocal Microscopy and 3D Reconstructions.

作者信息

Seidel T, Edelmann J-C, Sachse F B

机构信息

Nora Eccles Harrison Cardiovascular Research and Training Institute, University of Utah, 95 South 2000 East, Salt Lake City, UT 84112-5000, USA.

Institute of Biomedical Engineering, Karlsruhe Institute of Technology, Fritz-Haber-Weg 1, 76131 Karlsruhe, Germany.

出版信息

Ann Biomed Eng. 2016 May;44(5):1436-1448. doi: 10.1007/s10439-015-1465-6. Epub 2015 Sep 23.

DOI:10.1007/s10439-015-1465-6
PMID:26399990
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4805509/
Abstract

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 µm. 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.

摘要

心脏组织的微观结构表征及其在疾病中的重塑是许多基础研究项目中的关键步骤。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固定方法以及标记和成像方案,便于通过扫描共聚焦显微镜获取三维图像堆栈。我们用正常和梗死的心室组织评估了该方法。我们将获取的图像堆栈用于重要组织成分的分割、定量分析和可视化。与传统固定方法相比,无压缩固定保留了细胞形状、毛细血管腔和细胞外板层。此外,新方法和成像方案在深度达60 µm时产生了高信噪比。这使得能够进行广泛分析,揭示对照与梗死边缘区中心肌细胞、血管、成纤维细胞、肌成纤维细胞和细胞外空间的体积分数和分布的主要差异。我们的结果表明,所开发的方法产生了关于心脏组织微观结构及其在疾病中重塑的全面数据。与其他方法相比,它允许对所有主要组织成分进行定量评估。此外,我们认为该方法将为亚微米尺度上的心脏组织生理模型提供重要数据。