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色素上皮衍生因子缺失使C57BL/6J小鼠对光诱导的视网膜损伤敏感。

Loss of Pigment Epithelium Derived Factor Sensitizes C57BL/6J Mice to Light-Induced Retinal Damage.

作者信息

Shelton Debresha A, Papania Jack T, Getz Tatiana E, Sellers Jana T, Giradot Preston E, Chrenek Micah A, Grossniklaus Hans E, Boatright Jeffrey H, Nickerson John M

机构信息

Department of Ophthalmology, Emory University, Atlanta, Georgia, United States.

Atlanta Veterans Administration Center for Visual and Neurocognitive Rehabilitation, Decatur, Georgia, United States.

出版信息

bioRxiv. 2024 Dec 4:2024.12.04.626802. doi: 10.1101/2024.12.04.626802.

Abstract

PURPOSE

Pigment epithelium-derived factor (PEDF) is a neurotrophic glycoprotein secreted by the retinal pigment epithelium (RPE) that supports retinal photoreceptor health. Deficits in PEDF are associated with increased inflammation and retinal degeneration in aging and diabetic retinopathy. We hypothesized that light-induced stress in C57BL/6J mice deficient in PEDF would lead to increased retinal neuronal and RPE defects, impaired expression of neurotrophic factor Insulin-like growth factor 1 (IGF-1), and overactivation of Galectin-3-mediated inflammatory signaling.

METHODS

C57BL/6J mice expressing the RPE65 M450/M450 allele were crossed to PEDF and wildtype (PEDF ) littermates. Mice were exposed to 50,000 lux light for 5 hours to initiate acute damage. Changes in visual function outcomes were tracked via electroretinogram (ERG), confocal scanning laser ophthalmoscopy(cSLO), and spectral domain optical coherence tomography (SD-OCT) on days 3, 5, and 7 post-light exposure. Gene and protein expression of Galectin-3 were measured by digital drop PCR (ddPCR) and western blot. To further investigate the role of galectin-3 on visual outcomes and PEDF expression after damage, we also used a small-molecule inhibitor to reduce its activity.

RESULTS

Following light damage, PEDF mice showed more severe retinal thinning, impaired visual function (reduced a-, b-, and c-wave amplitudes), and increased Galectin-3 expressing immune cell infiltration compared to PEDF . PEDF mice had suppressed damage-associated increases in IGF-1 expression. Additionally, baseline Galectin-3 mRNA and protein expression were reduced in PEDF mice compared to PEDF . However, after light damage, Galectin-3 expression decreases in PEDF mice but increases in PEDF KO/KO mice without reaching PEDF levels. Galectin-3 inhibition worsens retinal degeneration, reduces PEDF expression in PEDF mice, and mimics the effects seen in PEDF knockouts.

CONCLUSIONS

Loss of PEDF alone does not elicit functional defects in C57BL/6J mice. However, under light stress, PEDF deficiency significantly increases severe retinal degeneration, visual deficits, Galectin-3 expression, and suppression of IGF-1 than PEDF . PEDF deficiency reduced baseline expression of Galectin-3, and pharmacological inhibition of Galectin-3 worsens outcomes and suppresses PEDF expression in PEDF , suggesting a novel co-regulatory relationship between the two proteins in mitigating light-induced retinal damage.

摘要

目的

色素上皮衍生因子(PEDF)是一种由视网膜色素上皮(RPE)分泌的神经营养糖蛋白,可维持视网膜光感受器的健康。PEDF缺乏与衰老和糖尿病视网膜病变中炎症增加及视网膜变性有关。我们推测,在缺乏PEDF的C57BL/6J小鼠中,光诱导的应激会导致视网膜神经元和RPE缺陷增加、神经营养因子胰岛素样生长因子1(IGF-1)表达受损以及半乳糖凝集素-3介导的炎症信号过度激活。

方法

将表达RPE65 M450/M450等位基因的C57BL/6J小鼠与PEDF 及野生型(PEDF )同窝小鼠杂交。小鼠暴露于50,000勒克斯光照下5小时以引发急性损伤。在光照后第3、5和7天,通过视网膜电图(ERG)、共焦扫描激光检眼镜(cSLO)和光谱域光学相干断层扫描(SD-OCT)追踪视觉功能结果的变化。通过数字液滴PCR(ddPCR)和蛋白质免疫印迹法检测半乳糖凝集素-3的基因和蛋白表达。为了进一步研究半乳糖凝集素-3在损伤后对视觉结果和PEDF表达的作用,我们还使用了一种小分子抑制剂来降低其活性。

结果

与PEDF 小鼠相比,光照损伤后,PEDF 小鼠表现出更严重的视网膜变薄、视觉功能受损(a波、b波和c波振幅降低)以及表达半乳糖凝集素-3的免疫细胞浸润增加。PEDF 小鼠损伤相关的IGF-1表达增加受到抑制。此外,与PEDF 小鼠相比,PEDF 小鼠的基线半乳糖凝集素-3 mRNA和蛋白表达降低。然而,光照损伤后,PEDF 小鼠的半乳糖凝集素-3表达降低,而PEDF KO/KO小鼠的半乳糖凝集素-3表达增加,但未达到PEDF 小鼠的水平。抑制半乳糖凝集素-3会加重视网膜变性,降低PEDF 小鼠中PEDF的表达,并模拟PEDF基因敲除小鼠的表现。

结论

单独缺失PEDF不会在C57BL/6J小鼠中引发功能缺陷。然而,在光应激下,与PEDF 小鼠相比,PEDF缺乏会显著增加严重的视网膜变性、视觉缺陷、半乳糖凝集素-3表达以及IGF-1的抑制。PEDF缺乏降低了半乳糖凝集素-3的基线表达,对半乳糖凝集素-3的药理抑制会使结果恶化并抑制PEDF 小鼠中PEDF的表达,这表明这两种蛋白在减轻光诱导的视网膜损伤方面存在新的共同调节关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7944/11643041/d48591263a40/nihpp-2024.12.04.626802v1-f0001.jpg

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