Departments of Ophthalmology and Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Sci Rep. 2018 Apr 23;8(1):6371. doi: 10.1038/s41598-018-24197-2.
Vitreous or aqueous humour taps are widely used in patients or large animals with retinal diseases to monitor disease biomarkers, search for novel biomarkers, assess the integrity of the blood-retinal barrier, or perform pharmacokinetic or pharmacodynamics studies. Although there are many useful mouse models of retinal diseases, the small size of mouse eyes has precluded vitreous or aqueous taps. Herein we describe a novel technique, mousetap, which allows collection of vitreous or aqueous humour uncontaminated by blood or tissue surrounding the vitreous cavity. Mousetap was used to obtain vitreous samples from several mouse models of retinal vascular diseases and vitreous albumin measured by ELISA was highly reproducible among mice of the same model. The mean vitreous albumin concentration differed widely among control mice and mice of different models and correlated with fluorescein angiographic assessment of vascular leakage severity. Protein arrays showed increases in levels of several vasoactive proteins in the vitreous from mice with oxygen-induced ischemic retinopathy compared with age-matched controls; almost all of these proteins are increased in the vitreous of patients with the most common human ischemic retinopathy, proliferative diabetic retinopathy. Thus, mousetap facilitates the use of mice for studies previously reserved for large animal models and patients.
玻璃体或房水抽取广泛应用于患有视网膜疾病的患者或大型动物中,以监测疾病生物标志物、寻找新的生物标志物、评估血视网膜屏障的完整性,或进行药代动力学或药效动力学研究。虽然有许多有用的视网膜疾病小鼠模型,但小鼠眼睛的体积小,无法进行玻璃体或房水抽取。本文描述了一种新的技术,即 mousetap,可以采集不受玻璃体腔周围血液或组织污染的玻璃体或房水样本。mousetap 用于从几种视网膜血管疾病的小鼠模型中获得玻璃体样本,通过 ELISA 测量的玻璃体白蛋白在同一种模型的小鼠之间具有高度可重复性。在不同模型的对照小鼠和小鼠之间,玻璃体白蛋白的平均浓度差异很大,与荧光素血管造影评估的血管渗漏严重程度相关。蛋白质阵列显示,与年龄匹配的对照相比,来自氧诱导缺血性视网膜病变小鼠的玻璃体中几种血管活性蛋白的水平增加;几乎所有这些蛋白质在最常见的人类缺血性视网膜病变、增生性糖尿病性视网膜病变患者的玻璃体中均增加。因此,mousetap 促进了将小鼠用于以前仅保留给大型动物模型和患者的研究。