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Efemp1基因缺失对小鼠眼视网膜色素上皮下沉积物的形成具有保护作用。

Deletion of Efemp1 Is Protective Against the Development of Sub-RPE Deposits in Mouse Eyes.

作者信息

Stanton James B, Marmorstein Alan D, Zhang Youwen, Marmorstein Lihua Y

机构信息

Department of Ophthalmology & Vision Science, University of Arizona, Tucson, Arizona, United States.

Department of Ophthalmology, Mayo Clinic, Rochester, Minnesota, United States.

出版信息

Invest Ophthalmol Vis Sci. 2017 Mar 1;58(3):1455-1461. doi: 10.1167/iovs.16-20955.

Abstract

PURPOSE

EFEMP1 (fibulin-3) is mutated in Malattia Leventinese/Doyne's honeycomb retinal dystrophy (ML/DHRD), an inherited macular dystrophy similar to AMD. Both ML/DHRD and AMD are characterized by the presence of sub-RPE deposits. Efemp1 knockout mice do not develop sub-RPE deposits. This study was to test whether sub-RPE deposits can be induced in Efemp1 knockout mice by experimentally applied stress conditions that cause wild-type mice to develop sub-RPE deposits.

METHODS

Efemp1 knockout and control mice at 6, 18, or 24 months old were fed with a synthetic high-fat diet (HFD). Beginning 1 month after starting the HFD, one group of mice was exposed to cigarette smoke daily for 1 month, and another group of mice was subjected to photochemical injury every other day for 2 weeks from a 488-nm argon laser. After the treatments, histologic analysis was performed to assess whether sub-RPE deposits were induced.

RESULTS

Basal laminar deposits (BLamDs), a form of sub-RPE deposits, were observed in the 18- and 24-month-old wild-type mice but not in Efemp1 knockout mice in any age groups after exposure to HFD and cigarette smoke or laser injury.

CONCLUSIONS

Mice lacking fibulin-3 do not develop sub-RPE deposits. Environmental oxidative stressors (HFD/cigarette smoke or HFD/laser) known to cause BLamD formation in wild-type mice failed to induce BLamD formation in Efemp1 knockout mice. These results suggest that fibulin-3 is a central player in the development of BLamD, and deletion of fibulin-3 is protective against the development of BLamD.

摘要

目的

EFEMP1(纤维连接蛋白-3)在莱文廷斯病/多伊内蜂窝状视网膜营养不良(ML/DHRD)中发生突变,这是一种与年龄相关性黄斑变性(AMD)相似的遗传性黄斑营养不良。ML/DHRD和AMD均以视网膜色素上皮(RPE)下沉积物的存在为特征。Efemp1基因敲除小鼠不会形成RPE下沉积物。本研究旨在测试通过实验施加导致野生型小鼠形成RPE下沉积物的应激条件,是否能在Efemp1基因敲除小鼠中诱导形成RPE下沉积物。

方法

给6、18或24月龄的Efemp1基因敲除小鼠和对照小鼠喂食合成高脂饮食(HFD)。从开始喂食HFD 1个月后,一组小鼠每天暴露于香烟烟雾中1个月,另一组小鼠每隔一天接受488nm氩激光进行光化学损伤,持续2周。处理后,进行组织学分析以评估是否诱导形成了RPE下沉积物。

结果

在18和24月龄的野生型小鼠中观察到了基底膜沉积物(BLamDs),这是RPE下沉积物的一种形式,但在任何年龄组的Efemp1基因敲除小鼠中,在暴露于HFD和香烟烟雾或激光损伤后均未观察到。

结论

缺乏纤维连接蛋白-3的小鼠不会形成RPE下沉积物。已知在野生型小鼠中会导致BLamD形成的环境氧化应激源(HFD/香烟烟雾或HFD/激光)未能在Efemp1基因敲除小鼠中诱导BLamD形成。这些结果表明,纤维连接蛋白-3是BLamD形成过程中的关键因素,纤维连接蛋白-3的缺失对BLamD的形成具有保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/340a/5361459/8301a21e0d80/i1552-5783-58-3-1455-f01.jpg

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