Hammer Daniel X, Liu Zhuolin, Cava Jenna A, Carroll Joseph, Saeedi Osamah
Division of Biomedical Physics, Office of Science and Engineering Laboratories, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Avenue, Silver Spring, MD, 20993, USA.
Department of Ophthalmology and Visual Sciences, Medical College of Wisconsin, 925 N. 87th Street, Milwaukee, WI, 53226, USA.
Am J Ophthalmol Case Rep. 2020 Jun 1;19:100757. doi: 10.1016/j.ajoc.2020.100757. eCollection 2020 Sep.
To determine the axial location of Gunn's dots in the retina.
Adaptive optics scanning laser ophthalmoscopy (AOSLO) images and adaptive optics - optical coherence tomography (AO-OCT) volumes were collected from a region where Gunn's dots were found inferior to the optic disc from a subject determined by clinical examination to be a glaucoma suspect. AO-OCT volumes were also collected along the horizontal and vertical meridians from six healthy subjects and one glaucoma subject to identify and document other occurrences of Gunn's dots. AO-OCT volumes were registered in three-dimensions and averaged. Gunn's dots were segmented, and their volume, area, and diameter were measured.
All Gunn's dots imaged in this study from all subjects were confined to the inner limiting membrane, neither extending into the vitreous nor into the nerve fiber layer. The size of the dots was highly variable. The measured volume, area, and diameter (mean ± standard deviation) were 1119.9 ± 590.9 μm, 220.2 ± 105.5 μm, and 14.3 ± 3.1 μm, the latter within the range as previously published reports.
Based upon evidence from this study and others, Gunn's dots are not thought to be Müller cell end-feet or hyalocytes. We hypothesize that they are related to microglia, either as the by-product of their phagocytosis function, or are actual dead ameboid-shaped microglia who have fulfilled their scavenger role in retinal pathology. Further studies are needed in diseased eyes to determine if they have predictive value.
确定视网膜中 Gunn 点的轴向位置。
从一名经临床检查确定为青光眼疑似患者的视盘下方发现 Gunn 点的区域收集自适应光学扫描激光检眼镜(AOSLO)图像和自适应光学光学相干断层扫描(AO-OCT)容积数据。还从六名健康受试者和一名青光眼受试者的水平和垂直子午线方向收集 AO-OCT 容积数据,以识别和记录 Gunn 点的其他出现情况。对 AO-OCT 容积数据进行三维配准并求平均值。对 Gunn 点进行分割,并测量其容积、面积和直径。
本研究中所有受试者成像的所有 Gunn 点均局限于内界膜,既不延伸至玻璃体也不延伸至神经纤维层。这些点的大小差异很大。测量的容积、面积和直径(平均值±标准差)分别为 1119.9±590.9μm、220.2±105.5μm 和 14.3±3.1μm,后者在先前发表报告的范围内。
基于本研究及其他研究的证据,Gunn 点不被认为是 Müller 细胞终足或玻璃体细胞。我们假设它们与小胶质细胞有关,要么是其吞噬功能的副产物,要么是在视网膜病变中已完成清除作用的实际死亡的阿米巴样小胶质细胞。需要对患病眼睛进行进一步研究以确定它们是否具有预测价值。