Goebel Collin P, Song Yong-Seok, Zaitoun Ismail S, Wang Shoujian, Potter Heather A D, Sorenson Christine M, Sheibani Nader
Department of Ophthalmology and Visual Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
McPherson Eye Research Institute, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
J Ophthalmic Vis Res. 2023 Feb 21;18(1):51-59. doi: 10.18502/jovr.v18i1.12725. eCollection 2023 Jan-Mar.
Adenosine signaling modulates ocular inflammatory processes, and its antagonism mitigates neovascularization in both newborns and preclinical models of ocular neovascularization including age-related macular degeneration (AMD). The adenosine receptor expression patterns have not been well characterized in the human retina and choroid.
Here we examined the expression of adenosine receptor subtypes within the retina and choroid of human donor eyes with and without AMD. Antibodies specifically targeting adenosine receptor subtypes A1, A2A, A2B, and A3 were used to assess their expression patterns. Quantitative real-time PCR analysis was used to confirm gene expression of these receptors within the normal human retina and choroid.
We found that all four receptor subtypes were expressed in several layers of the retina, and within the retinal pigment epithelium and choroid. The expression of A1 receptors was more prominent in the inner and outer plexiform layers, where microglia normally reside, and supported by RNA expression in the retina. A2A and A2B showed similar expression patterns with prominent expression in the vasculature and retinal pigment epithelium. No dramatic differences in expression of these receptors were observed in eyes from patients with dry or wet AMD compared to control, with the exception A3 receptors. Eyes with dry AMD lost expression of A3 in the photoreceptor outer segments compared with eyes from control or wet AMD.
The ocular presence of adenosine receptors is consistent with their proposed role in modulation of inflammation in both the retina and choroid, and their potential targeting for AMD treatment.
腺苷信号传导调节眼部炎症过程,其拮抗作用可减轻新生儿以及包括年龄相关性黄斑变性(AMD)在内的眼部新生血管形成临床前模型中的新生血管形成。腺苷受体在人类视网膜和脉络膜中的表达模式尚未得到充分表征。
在此,我们检测了患有和未患有AMD的人类供体眼视网膜和脉络膜中腺苷受体亚型的表达。使用特异性靶向腺苷受体亚型A1、A2A、A2B和A3的抗体来评估它们的表达模式。采用定量实时PCR分析来确认这些受体在正常人类视网膜和脉络膜中的基因表达。
我们发现所有四种受体亚型均在视网膜的几层、视网膜色素上皮和脉络膜中表达。A1受体的表达在内、外丛状层中更为突出,小胶质细胞通常驻留在这些层中,并且在视网膜中的RNA表达也支持这一点。A2A和A2B表现出相似的表达模式,在脉管系统和视网膜色素上皮中表达突出。与对照组相比,在干性或湿性AMD患者的眼中,除了A3受体外,未观察到这些受体表达的显著差异。与对照组或湿性AMD患者的眼睛相比,干性AMD患者的眼睛在光感受器外段失去了A3的表达。
眼部存在腺苷受体与其在调节视网膜和脉络膜炎症中的作用以及它们作为AMD治疗潜在靶点的作用一致。