Characterization of the Most Resistant and Vulnerable Retinal Ganglion Cell Subtypes in a Chronic Model of Glaucoma in Rat.

IF 4.7 2区 医学 Q1 OPHTHALMOLOGY
Noelia Ruzafa, Xandra Pereiro, Laura Prieto-López, Aritz Urcola, Arantxa Acera, Elena Vecino
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Abstract

Purpose: Retinal ganglion cells (RGCs) transmit visual information to the brain and are selectively affected in glaucoma, a neurodegenerative disease caused by increased intraocular pressure (IOP) leading to vision loss. Not all RGC subtypes are equally vulnerable; thus, this study aimed to comprehensively analyze the differential loss of RGC subtypes using a rat model of chronic glaucoma.

Methods: A chronic glaucoma model was established by cauterizing three episcleral veins in rat eyes. IOP was measured using an applanation tonometer, and after 40 days animals were euthanized. Whole-mount retinas were immunostained. RGCs were labeled with anti-RNA-binding protein with multiple splicing (RBPMS; marks 100% of RGCs) and co-labeled with subtype-specific antibodies: CART, melanopsin (OPN4), Foxp2, Islet1/2, SPP1, and Tbr2. RGC loss and subtype distribution were quantified as percentages of RBPMS-positive cells in different retinal regions.

Results: In glaucomatous eyes, RGC survival decreased in the retinal periphery, with 65.44% in the dorsal-nasal and 76.03% in the ventral-temporal regions. CART-positive RGCs dropped from 32.9% ± 5.15% to 20.26% ± 2.64% (dorsal-nasal) and from 33.07% ± 4.09% to 22.65% ± 2.65% (ventral-temporal), indicating higher vulnerability. In contrast, OPN4-positive RGCs increased from 3.27% ± 1.34% to 6.99% ± 2.31% (dorsal-nasal), suggesting greater intrinsically photosensitive RGC (ipRGC) resilience. Percentages of SPP1-, Foxp2-, Islet1/2-, and Tbr2-positive RGCs remained unchanged, suggesting proportional loss to total RGC reduction.

Conclusions: RGC subtypes showed differing susceptibilities to IOP, with OPN4-positive RGCs (ipRGCs) being more resistant and CART-positive RGCs (ON-OFF direction-selective ganglion cells [ooDSGCs]) highly vulnerable. This highlights the need to study ooDSGC degeneration and explore targeted neuroprotection. Future research should develop therapies to protect, regenerate, or replace ooDSGCs.

慢性青光眼大鼠视网膜神经节细胞最耐药和最易感亚型的特征。
目的:视网膜神经节细胞(RGCs)向大脑传递视觉信息,并在青光眼中选择性地受到影响,青光眼是一种由眼压升高(IOP)导致视力丧失的神经退行性疾病。并非所有的RGC亚型都同样脆弱;因此,本研究旨在利用慢性青光眼大鼠模型,全面分析RGC亚型的差异损失。方法:采用烧灼大鼠眼外三静脉的方法建立慢性青光眼模型。用眼压计测量眼压,40天后对动物实施安乐死。对整个视网膜进行免疫染色。RGCs用多重剪接抗rna结合蛋白(RBPMS,标记100% RGCs)标记,并与亚型特异性抗体CART、黑视素(OPN4)、Foxp2、Islet1/2、SPP1和Tbr2共同标记。RGC损失和亚型分布以rbpms阳性细胞在不同视网膜区域的百分比进行量化。结果:青光眼视网膜周围RGC存活率下降,鼻背区为65.44%,腹颞区为76.03%。cart阳性RGCs从32.9%±5.15%下降到20.26%±2.64%(背侧-鼻腔),从33.07%±4.09%下降到22.65%±2.65%(腹侧-颞部),表明脆弱性较高。相比之下,opn4阳性RGC从3.27%±1.34%增加到6.99%±2.31%(背鼻),表明RGC (ipRGC)具有更强的内在光敏性。SPP1-、Foxp2-、Islet1/2-和tbr2阳性RGC的百分比保持不变,表明RGC总量减少成比例。结论:RGC亚型对IOP的易感性不同,其中opn4阳性RGC (iprgc)更耐药,而cart阳性RGC (ON-OFF方向选择性神经节细胞[ooDSGCs])易感。这突出了研究ooDSGC变性和探索靶向神经保护的必要性。未来的研究应该开发出保护、再生或替代ooDSGCs的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.90
自引率
4.50%
发文量
339
审稿时长
1 months
期刊介绍: Investigative Ophthalmology & Visual Science (IOVS), published as ready online, is a peer-reviewed academic journal of the Association for Research in Vision and Ophthalmology (ARVO). IOVS features original research, mostly pertaining to clinical and laboratory ophthalmology and vision research in general.
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