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使用非侵入性荧光分子成像技术可视化肺部炎症

Visualization of pulmonary inflammation using noninvasive fluorescence molecular imaging.

作者信息

Haller Jodi, Hyde Damon, Deliolanis Nikolaos, de Kleine Ruben, Niedre Mark, Ntziachristos Vasilis

机构信息

Center for Molecular Imaging Research Laboratory For Bio-optics and Molecular Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, USA.

出版信息

J Appl Physiol (1985). 2008 Mar;104(3):795-802. doi: 10.1152/japplphysiol.00959.2007. Epub 2008 Jan 17.

Abstract

The ability to visualize molecular processes and cellular regulators of complex pulmonary diseases such as asthma, chronic obstructive pulmonary disease (COPD), or adult respiratory distress syndrome (ARDS), would aid in the diagnosis, differentiation, therapy assessment and in small animal-based drug-discovery processes. Herein we report the application of normalized transillumination and fluorescence molecular tomography (FMT) for the noninvasive quantitative imaging of the mouse lung in vivo. We demonstrate the ability to visualize and quantitate pulmonary response in a murine model of LPS-induced airway inflammation. Twenty-four hours prior to imaging, BALB/c female mice were injected via tail vein with 2 nmol of a cathepsin-sensitive activatable fluorescent probe (excitation: 750 nm; emission: 780 nm) and 2 nmol of accompanying intravascular agent (excitation: 674 nm; emission: 694 nm). Six hours later, the mice were anesthetized with isoflurane and administered intranasal LPS in sterile 0.9% saline in 25 microl aliquots (one per nostril). Fluorescence molecular imaging revealed the in vivo profile of cysteine protease activation and vascular distribution within the lung typifying the inflammatory response to LPS insult. Results were correlated with standard in vitro laboratory tests (Western blot, bronchoalveolar lavage or BAL analysis, immunohistochemistry) and revealed good correlation with the underlying activity. We demonstrated the capacity of fluorescence tomography to noninvasively and longitudinally characterize physiological, cellular, and subcellular processes associated with inflammatory disease burden in the lung. The data presented herein serve to further evince fluorescence molecular imaging as a technology highly appropriate for the biomedical laboratory.

摘要

可视化诸如哮喘、慢性阻塞性肺疾病(COPD)或成人呼吸窘迫综合征(ARDS)等复杂肺部疾病的分子过程和细胞调节因子的能力,将有助于诊断、鉴别、治疗评估以及基于小动物的药物发现过程。在此,我们报告了归一化透照和荧光分子断层扫描(FMT)在小鼠肺活体无创定量成像中的应用。我们展示了在脂多糖(LPS)诱导的气道炎症小鼠模型中可视化和定量肺部反应的能力。在成像前24小时,通过尾静脉向BALB/c雌性小鼠注射2 nmol组织蛋白酶敏感的可激活荧光探针(激发波长:750 nm;发射波长:780 nm)和2 nmol伴随的血管内试剂(激发波长:674 nm;发射波长:694 nm)。6小时后,用异氟烷麻醉小鼠,并以25微升等分试样(每个鼻孔一份)的无菌0.9%盐水经鼻给予LPS。荧光分子成像揭示了肺内半胱氨酸蛋白酶激活和血管分布的活体情况,代表了对LPS损伤的炎症反应。结果与标准体外实验室检测(蛋白质免疫印迹法、支气管肺泡灌洗或BAL分析、免疫组织化学)相关,显示与潜在活性具有良好的相关性。我们证明了荧光断层扫描能够无创且纵向地表征与肺部炎症疾病负担相关的生理、细胞和亚细胞过程。本文所呈现的数据进一步证明了荧光分子成像作为一种非常适合生物医学实验室的技术。

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