Villafuerte-Trisolini Carol, Le Sophie M, Sin Tzu-Ni, Huynh Leon, Gong Megan, Shen Tony, Heo Jaewon, Roszak Karolina, Raposo Ana Santos, Graham James, Havel Peter, Choy Kevin, Farsiu Sina, Thomasy Sara M, Yiu Glenn
Department of Ophthalmology & Vision Science, University of California, Davis, Davis, California, United States.
Department of Surgical & Radiological Sciences, School of Veterinary Medicine, University of California, Davis, Davis, California, United States.
Invest Ophthalmol Vis Sci. 2025 Sep 2;66(12):41. doi: 10.1167/iovs.66.12.41.
Lipids are a principal component of drusen and are involved in the pathobiology of age-related macular degeneration (AMD). Nonhuman primates (NHPs) develop macular drusen and may provide insight into circulating or local lipids in AMD.
We evaluated aged rhesus macaques by fundus photography, optical coherence tomography (OCT), and fundus autofluorescence, as well as measured fasting plasma glucose, total cholesterol, high- and low-density lipoproteins, triglycerides, and apolipoprotein (Apo) A1, B, CIII, and E. Retinal tissues were collected for electron microscopy and immunostained for oil red O, ApoE, and ApoB.
Among 203 adult macaques (mean age 19.1 ± 3.1 years), 25 animals (12.1%) exhibited soft drusen with sub-RPE deposits, while 59 (28.6%) had yellow punctate dots that were mostly hyperautofluorescent without RPE elevation on OCT. Drusen prevalence increased with older age (P = 0.001) but not with plasma lipids (P > 0.05 for all), while the punctate dot phenotype was associated with older age (P = 0.014), higher fasting glucose (P = 0.023), low-density lipoprotein cholesterol (P = 0.022), and ApoB (P = 0.017). Ultrastructure revealed NHP drusen consisting of extracellular sub-RPE lipid particles, whereas punctate dots appeared to correspond to individual RPE cells with intracellular lipid vacuoles. Both sub-RPE and intra-RPE lipids of the two phenotypes contained neutral lipids and ApoE, while ApoE and ApoB appeared to be expressed in RPE.
In rhesus macaques, soft drusen are extracellular lipid deposits associated with older age, while punctate dots are intracellular lipids linked to age, hyperglycemia, and hyperlipidemia, suggesting differential dysregulation of lipid transport in these NHP models of AMD.
脂质是玻璃膜疣的主要成分,参与年龄相关性黄斑变性(AMD)的病理生物学过程。非人灵长类动物(NHPs)会出现黄斑玻璃膜疣,可能有助于深入了解AMD患者的循环脂质或局部脂质情况。
我们通过眼底照相、光学相干断层扫描(OCT)和眼底自发荧光对老年恒河猴进行评估,并测量空腹血糖、总胆固醇、高密度和低密度脂蛋白、甘油三酯以及载脂蛋白(Apo)A1、B、CIII和E。收集视网膜组织用于电子显微镜检查,并进行油红O、ApoE和ApoB免疫染色。
在203只成年猕猴(平均年龄19.1±3.1岁)中,25只动物(12.1%)出现伴有视网膜色素上皮(RPE)下沉积物的软性玻璃膜疣,而59只(28.6%)有黄色点状斑点,在OCT上大多为高自发荧光且无RPE抬高。玻璃膜疣患病率随年龄增长而增加(P = 0.001),但与血脂无关(所有P>0.05),而点状斑点表型与年龄较大(P = 0.014)、空腹血糖较高(P = 0.023)、低密度脂蛋白胆固醇(P = 0.022)和ApoB(P = 0.017)相关。超微结构显示NHPs玻璃膜疣由细胞外RPE下脂质颗粒组成,而点状斑点似乎对应于具有细胞内脂质空泡的单个RPE细胞。两种表型的RPE下和RPE内脂质均含有中性脂质和ApoE,而ApoE和ApoB似乎在RPE中表达。
在恒河猴中,软性玻璃膜疣是与年龄相关的细胞外脂质沉积物,而点状斑点是与年龄、高血糖和高脂血症相关的细胞内脂质,提示在这些AMD的NHPs模型中脂质转运存在不同的失调情况。