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本文引用的文献

1
Visualization of pulmonary inflammation using noninvasive fluorescence molecular imaging.使用非侵入性荧光分子成像技术可视化肺部炎症
J Appl Physiol (1985). 2008 Mar;104(3):795-802. doi: 10.1152/japplphysiol.00959.2007. Epub 2008 Jan 17.
2
Experimental three-dimensional fluorescence reconstruction of diffuse media by use of a normalized Born approximation.利用归一化玻恩近似对漫射介质进行实验性三维荧光重建。
Opt Lett. 2001 Jun 15;26(12):893-5. doi: 10.1364/ol.26.000893.
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Fluorescence tomography and magnetic resonance imaging of myocardial macrophage infiltration in infarcted myocardium in vivo.体内梗死心肌中巨噬细胞浸润的荧光断层扫描和磁共振成像
Circulation. 2007 Mar 20;115(11):1384-91. doi: 10.1161/CIRCULATIONAHA.106.663351. Epub 2007 Mar 5.
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Time-resolved imaging of optical coefficients through murine chest cavities.通过小鼠胸腔对光学系数进行时间分辨成像。
J Biomed Opt. 2006 Nov-Dec;11(6):064017. doi: 10.1117/1.2400702.
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From finite to infinite volumes: removal of boundaries in diffuse wave imaging.从有限体积到无限体积:漫射波成像中边界的去除
Phys Rev Lett. 2006 May 5;96(17):173903. doi: 10.1103/PhysRevLett.96.173903. Epub 2006 May 4.
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Accuracy of fluorescent tomography in the presence of heterogeneities: study of the normalized Born ratio.存在异质性时荧光断层扫描的准确性:归一化博恩比率研究
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Looking and listening to light: the evolution of whole-body photonic imaging.观察与聆听光线:全身光子成像的发展历程
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Experimental fluorescence tomography of tissues with noncontact measurements.非接触测量的组织实验性荧光断层扫描
IEEE Trans Med Imaging. 2004 Apr;23(4):492-500. doi: 10.1109/TMI.2004.825633.
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Singular-value analysis and optimization of experimental parameters in fluorescence molecular tomography.荧光分子断层成像中实验参数的奇异值分析与优化
J Opt Soc Am A Opt Image Sci Vis. 2004 Feb;21(2):231-41. doi: 10.1364/josaa.21.000231.
10
Pathogenic role of matrix metalloproteases and their inhibitors in asthma and chronic obstructive pulmonary disease and therapeutic relevance of matrix metalloproteases inhibitors.基质金属蛋白酶及其抑制剂在哮喘和慢性阻塞性肺疾病中的致病作用以及基质金属蛋白酶抑制剂的治疗意义。
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肺部炎症中分子特征的光学成像。

Optical imaging of molecular signatures in pulmonary inflammation.

作者信息

Ntziachristos Vasilis

机构信息

Institute for Biological and Medical Imaging, Helmholtz Zentrum München and Technische Universität München, Munich, Germany.

出版信息

Proc Am Thorac Soc. 2009 Aug 15;6(5):416-8. doi: 10.1513/pats.200901-003AW.

DOI:10.1513/pats.200901-003AW
PMID:19687213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2731801/
Abstract

Biomedical imaging has become an important tool in the study of "-omics" fields by allowing the noninvasive visualization of functional and molecular events using in vivo staining and reporter gene approaches. This capacity can go beyond the understanding of the genetic basis and phenotype of such respiratory conditions as acute bronchitis, adult respiratory distress syndrome (ARDS), chronic obstructive pulmonary disease (COPD), and asthma and investigate the development of disease and of therapeutic events longitudinally and in unperturbed environments. Herein, we show how the application of novel quantitative optical imaging methods, using transillumination and fluorescence molecular tomography (FMT), can allow visualization of pulmonary inflammation in small animals in vivo. The results confirm prior observations using a protease-sensitive probe. We discuss how this approach enables in vivo insights at the system level as to the dynamic role of proteases in respiratory pathophysiology and their potential as therapeutic targets. Overall, the proposed imaging method can be used with a significantly wider range of possible targets and applications in lung imaging.

摘要

生物医学成像已成为“组学”领域研究中的一项重要工具,它通过体内染色和报告基因方法实现对功能和分子事件的无创可视化。这种能力不仅有助于理解诸如急性支气管炎、成人呼吸窘迫综合征(ARDS)、慢性阻塞性肺疾病(COPD)和哮喘等呼吸系统疾病的遗传基础和表型,还能在未受干扰的环境中纵向研究疾病的发展和治疗过程。在此,我们展示了如何应用新型定量光学成像方法,即透照和荧光分子断层扫描(FMT),在小动物体内实现肺部炎症的可视化。结果证实了先前使用蛋白酶敏感探针的观察结果。我们讨论了这种方法如何在系统层面深入了解蛋白酶在呼吸病理生理学中的动态作用及其作为治疗靶点的潜力。总体而言,所提出的成像方法可用于更广泛的肺部成像潜在靶点和应用。