Huang Xiang-Run, Knighton Robert W, Spector Ye Z, Feuer William J
a Bascom Palmer Eye Institute , Miller School of Medicine University of Miami , Miami , FL , USA.
b Department of Biomedical Engineering , College of Engineering University of Miami , Coral Gables , FL , USA.
Curr Eye Res. 2017 Jun;42(6):936-947. doi: 10.1080/02713683.2016.1262043. Epub 2017 Jan 17.
Glaucoma damages the retinal nerve fiber layer (RNFL). Both RNFL thickness and retardance can be used to assess the damage, but birefringence, the ratio of retardance to thickness, is a property of the tissue itself. This study investigated the relationship between axonal cytoskeleton and RNFL birefringence in retinas with hypertensive damage.
High intraocular pressure (IOP) was induced unilaterally in rat eyes. RNFL retardance in isolated retinas was measured. Cytostructural organization and bundle thickness were evaluated by confocal imaging of immunohistochemical staining of the cytoskeletal components: microtubules (MTs), F-actin, and neurofilaments. Bundles with different appearances of MT stain were studied, and their birefringence was calculated at different radii from the optic nerve head (ONH) center.
Forty bundles in eight normal retinas and 37 bundles in 10 treated retinas were examined. In normal retinas, the stain of axonal cytoskeleton was approximately uniform within bundles, and RNFL birefringence did not change along bundles. In treated retinas, elevation of IOP caused non-uniform alteration of axonal cytoskeleton across the retina, and distortion of axonal MTs was associated with decreased birefringence. The study further demonstrated that change of RNFL birefringence profiles along bundles can imply altered axonal cytoskeleton, suggesting that ultrastructural change of the RNFL can be inferred from clinical measurements of RNFL birefringence. The study also demonstrated that measuring RNFL birefringence profiles along bundles, instead of at a single location, may provide a more sensitive way to detect axonal ultrastructural change.
Measurement of RNFL birefringence along bundles can provide estimation of cytoskeleton alteration and sensitive detection of glaucomatous damage.
青光眼会损害视网膜神经纤维层(RNFL)。RNFL厚度和延迟都可用于评估损伤情况,但双折射(延迟与厚度之比)是组织本身的一种特性。本研究调查了高血压性损伤视网膜中轴突细胞骨架与RNFL双折射之间的关系。
在大鼠单侧眼睛中诱导高眼压(IOP)。测量分离视网膜中RNFL的延迟。通过对细胞骨架成分(微管(MTs)、F - 肌动蛋白和神经丝)的免疫组织化学染色进行共聚焦成像,评估细胞结构组织和束厚度。研究了MT染色呈现不同外观的束,并在距视神经乳头(ONH)中心不同半径处计算其双折射。
检查了8个正常视网膜中的40个束和10个处理后视网膜中的37个束。在正常视网膜中,轴突细胞骨架在束内的染色大致均匀,并且RNFL双折射沿束不发生变化。在处理后的视网膜中,IOP升高导致整个视网膜轴突细胞骨架发生不均匀改变,轴突MTs的扭曲与双折射降低相关。该研究进一步表明,RNFL双折射沿束的变化情况可暗示轴突细胞骨架的改变,这表明可从RNFL双折射的临床测量中推断出RNFL的超微结构变化。该研究还表明,沿束测量RNFL双折射情况,而非在单个位置测量,可能提供一种更敏感的方法来检测轴突超微结构变化。
沿束测量RNFL双折射可提供细胞骨架改变的估计,并能敏感地检测青光眼性损伤。