Gupta Neeru, Fong Jessica, Ang Lee C, Yücel Yeni H
Department of Ophthalmology & Vision Sciences, University of Toronto, Toronto, Ontario, Canada.
Can J Ophthalmol. 2008 Feb;43(1):53-60. doi: 10.3129/i07-185.
Tau protein is a microtubule-associated protein critical to neuron structure and integrity. The abnormal hyperphosphorylated tau protein AT8 disrupts microtubules, interferes with axonal transport, and is associated with neuron injury in neurodegenerative diseases such as Alzheimer's disease. The purpose of this study was to assess the presence of tau protein and abnormal tau protein AT8 in human glaucomas and to determine whether abnormal tau protein plays a role in glaucomatous neural degeneration.
Sections from 11 surgical eye specimens with glaucoma from elevated intraocular pressure causes and 10 age-matched control eye specimens were immunostained for normal tau protein (BT2) and hyperphosphorylated tau protein (AT8). Postmortem specimens with incidental open-angle glaucoma (n = 6) were compared with controls (n = 3). Measurements of immunofluorescence intensity in glaucoma retinas were compared with those in control retinas. Abnormal tau AT8 and parvalbumin, a horizontal cell-specific marker, were studied with double-immunofluorescence techniques to determine colocalization.
In surgical glaucoma specimens, normal tau protein was decreased in both the optic nerve and retina compared with age-matched controls. Abnormal tau AT8 was evident within the posterior retina, predominantly at the outer border of the inner nuclear layer in surgical glaucoma specimens, and this was not observed in controls or incidental glaucoma cases. Quantitative immunofluorescence techniques demonstrated significantly increased abnormal tau AT8 in surgical glaucoma specimens compared with controls. Abnormal tau AT8 colocalized with parvalbumin in horizontal cells of the retina.
Abnormal tau AT8, a marker of injury in various neurological diseases, is present in human glaucomas with uncontrolled intraocular pressure. The finding of abnormal tau protein in retinal horizontal cells may relate to elevated intraocular pressure and (or) neural degeneration in glaucoma. Tau protein abnormality in glaucoma underscores shared pathways with other neurodegenerative diseases.
tau蛋白是一种对神经元结构和完整性至关重要的微管相关蛋白。异常的高磷酸化tau蛋白AT8会破坏微管,干扰轴突运输,并与阿尔茨海默病等神经退行性疾病中的神经元损伤有关。本研究的目的是评估tau蛋白和异常tau蛋白AT8在人类青光眼患者中的存在情况,并确定异常tau蛋白是否在青光眼性神经变性中起作用。
对11例因眼压升高导致青光眼的手术眼标本和10例年龄匹配的对照眼标本进行免疫染色,检测正常tau蛋白(BT2)和高磷酸化tau蛋白(AT8)。将偶发性开角型青光眼的尸检标本(n = 6)与对照标本(n = 3)进行比较。比较青光眼视网膜与对照视网膜的免疫荧光强度测量值。采用双重免疫荧光技术研究异常tau AT8和小白蛋白(一种水平细胞特异性标志物),以确定共定位情况。
在手术青光眼标本中,与年龄匹配的对照相比,视神经和视网膜中的正常tau蛋白均减少。异常tau AT8在手术青光眼标本的视网膜后部明显可见,主要位于内核层的外边界,而在对照或偶发性青光眼病例中未观察到这种情况。定量免疫荧光技术显示,与对照相比,手术青光眼标本中的异常tau AT8显著增加。异常tau AT8与视网膜水平细胞中的小白蛋白共定位。
异常tau AT8是各种神经疾病损伤的标志物,存在于眼压未得到控制的人类青光眼中。视网膜水平细胞中异常tau蛋白的发现可能与青光眼患者眼压升高和(或)神经变性有关。青光眼患者的tau蛋白异常突出了其与其他神经退行性疾病的共同途径。