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Quantitative measurement of lymphatic function in mice by noninvasive near-infrared imaging of a peripheral vein

机译:通过外周静脉无创近红外成像定量测量小鼠淋巴功能

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摘要

Optical imaging methods have been developed to measure lymphatic function in skin; however, the lymphatic system of many organs is not accessible to this technology. Since lymphatic transport of macromolecules from any organ proceeds to the blood circulation, we aimed to develop a method that can measure lymphatic function by monitoring the fluorescence in a superficial vein of an interstitially injected tracer. We selected a 40-kDa PEGylated near-infrared dye conjugate, as it showed lymphatic system–specific uptake and extended circulation in blood. Lymphatic transport to blood from subcutaneous tissue required a transit time before signal enhancement was seen in blood followed by a steady rise in signal over time. Increased lymphatic transport was apparent in awake mice compared with those under continuous anesthesia. The methods were validated in K14-VEGFR-3-Fc and K14-VEGF-C transgenic mice with loss and gain of lymphatic function, respectively. Reduced lymphatic transport to blood was also found in aged mice. The technique was also able to measure lymphatic transport from the peritoneal cavity, a location not suitable for optical imaging. The method is a promising, simple approach for assessment of lymphatic function and for monitoring of therapeutic regimens in mouse models of disease and may have potential for clinical translation.
机译:已经开发出光学成像方法来测量皮肤中的淋巴功能。但是,该技术无法访问许多器官的淋巴系统。由于大分子从任何器官的淋巴转运都进入血液循环,因此我们旨在开发一种方法,该方法可以通过监测间质注射示踪剂的浅静脉中的荧光来测量淋巴功能。我们选择了一种40 kDa聚乙二醇化的近红外染料偶联物,因为它显示了淋巴系统特异性摄取和血液中延长的循环。从皮下组织向血液的淋巴运输需要一段穿越时间,然后才能在血液中看到信号增强,然后信号随时间稳定上升。与持续麻醉的小鼠相比,清醒小鼠的淋巴运输增加。该方法在K14-VEGFR-3-Fc和K14-VEGF-C转基因小鼠中分别具有淋巴功能丧失和淋巴功能增强的方法得到验证。在老年小鼠中也发现淋巴运输到血液的减少。该技术还能够测量来自腹膜腔的淋巴转运,而腹膜腔不适用于光学成像。该方法是一种有前途的简单方法,可用于评估淋巴功能和监测疾病小鼠模型中的治疗方案,并且可能具有临床翻译潜力。

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