Ophthalmic Research Laboratories, Discipline of Ophthalmology and Visual Sciences, University of Adelaide, Level 7 Adelaide Health and Medical Sciences Building, North Terrace, Adelaide, SA, 5000, Australia.
Mol Neurobiol. 2022 Jan;59(1):117-136. doi: 10.1007/s12035-021-02582-9. Epub 2021 Oct 11.
Retinal detachment is a vision-threatening condition, which occurs when the neurosensory retina is separated from its blood supply. The main purpose of this study was to examine the effect of experimental retinal detachment in rats on cone photoreceptors. Retinal detachment was induced in the eyes of rats via subretinal injection of sodium hyaluronate. Experimental detachment caused a rapid, sustained loss of short (S)- and medium/long (M/L)-wavelength cone opsins. Importantly, S-opsin cones were affected earlier than M/L-opsin cones and were affected to a greater extent than M/L-opsin cones throughout the duration of detachment. In comparison, to cone opsins, reductions in other cone markers-peanut agglutinin PNA and cone arrestin-were substantially less marked. These data suggest that loss of cone opsins does not reflect cone degeneration and may rather indicate prolonged downregulation of specific proteins in affected cones. This conclusion is supported by the lack of TUNEL- cone arrestin double-labelled cells at the time point of greatest rod photoreceptor cell death, together with the partial recovery of cone arrestin cell numbers over time. Analysis of retinas that had naturally re-attached reinforced the deduction that few cones die following detachment, but also highlighted that prolonged detachment leads to deconstruction of cone segments that may not be readily reversible. Survival and functional recovery of cones following surgery for retinal detachment is vital for successful recovery of vision. The data suggest that experimental detachment in rats may offer a useful approach to model the response of S-cones to retinal detachment in humans.
视网膜脱离是一种威胁视力的疾病,当神经感觉视网膜与其血液供应分离时就会发生。本研究的主要目的是检查实验性大鼠视网膜脱离对视锥细胞的影响。通过视网膜下注射透明质酸钠在大鼠眼内诱发视网膜脱离。实验性脱离导致短(S)和中/长(M/L)波长视锥光感受蛋白迅速、持续丧失。重要的是,S-opsin 视锥细胞比 M/L-opsin 视锥细胞更早受到影响,并且在脱离的整个过程中受到的影响比 M/L-opsin 视锥细胞更大。相比之下,与视锥光感受蛋白相比,其他视锥细胞标志物-花生凝集素 PNA 和视锥细胞阻滞蛋白的减少要少得多。这些数据表明,视锥光感受蛋白的丧失并不反映视锥细胞的退化,而可能表明受影响的视锥细胞中特定蛋白质的长期下调。这一结论得到了以下事实的支持:在杆状细胞死亡最严重的时间点,TUNEL-视锥细胞阻滞蛋白双标记细胞缺失,并且随着时间的推移,视锥细胞阻滞蛋白细胞数量部分恢复。对自然重新附着的视网膜进行的分析进一步推断,在脱离后很少有视锥细胞死亡,但也强调了长时间的脱离会导致视锥细胞段的解体,这可能不容易逆转。在视网膜脱离手术后视锥细胞的存活和功能恢复对于成功恢复视力至关重要。数据表明,大鼠的实验性脱离可能为模拟人类 S-视锥细胞对视网膜脱离的反应提供一种有用的方法。