Ameboid Microglia as a Scavenger Role in Phagocytosis of Photoreceptor Outer Segment in an Experimental Retinal Detachment Model.

IF 5 2区 医学 Q1 OPHTHALMOLOGY
Manjing Cao, Yahan Zhang, Yan Li, Xian Zhang, Mingming Ma
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Abstract

Purpose: Photoreceptor (PR) death is the ultimate cause of irreversible vision loss in retinal detachment (RD). Previous studies have shown that microglia may have a dual role in RD. Nevertheless, the potential protective effects of microglia on PR are largely unknown. We aimed to uncover the phagocytic role of microglia in RD and propose a new concept to regulate PR survival.

Methods: An RD model was conducted by injecting sodium hyaluronate into the subretinal space (SRS) of C57BL/6J wild type mice. Bioinformatics analysis was used to evaluate the highly enriched pathways and terms relating to phagocytosis in human datasets and mouse transcriptomes of RD. The observation of microglial morphology was performed by immunofluorescence through cryosection and flat mount. PLX 3397 was used for microglial ablation. Phagocytosis of the outer segment (OS) by microglia was confirmed by immunofluorescence and hematoxylin and eosin staining. Expression of phagocytic markers in microglia was detected by immunofluorescence of cryosection. The PR survival was measured by TUNEL assay and hematoxylin and eosin staining. The optical coherence tomography (OCT) images through the center of the fovea in twelve patients were obtained to observe the clinic features of IS/OS dynamics after RD.

Results: The results showed that OS went through an accumulation-clearance process after RD. Ameboid microglia accumulated in the SRS and engulfed OS. Upregulation of phagocytic markers was observed in subretinal microglia. Depletion of microglia led to failure of OS clearance and retinal ruffling, which had the same characteristics as outer retinal undulation (ORU) in some patients with RD. PR did not benefit from microglial depletion, as no morphology and thickness recovery of PR was observed in the long term.

Conclusions: These results elucidate that microglial phagocytosis of OS is a critical process after RD. Insufficient phagocytosis leads to the accumulation of OS in the SRS and PR abnormalities. Appropriate regulation of microglial phagocytosis to remove OS may be a new concept to regulate photoreceptor survival.

实验性视网膜脱离模型中阿米巴样小胶质细胞在光感受器外段吞噬中的清除作用。
目的:光感受器(PR)死亡是视网膜脱离(RD)不可逆视力丧失的最终原因。先前的研究表明,小胶质细胞在RD中可能具有双重作用。然而,小胶质细胞对PR的潜在保护作用在很大程度上是未知的。我们旨在揭示小胶质细胞在RD中的吞噬作用,并提出调控PR存活的新概念。方法:采用透明质酸钠注入C57BL/6J野生型小鼠视网膜下腔(SRS),建立视网膜下腔视网膜下腔病变模型。利用生物信息学分析方法对人类数据集和小鼠RD转录组中与吞噬相关的高度富集的通路和术语进行评价。通过冷冻切片和平载免疫荧光观察小胶质细胞形态。PLX 3397用于小胶质细胞消融。免疫荧光、苏木精和伊红染色证实小胶质细胞吞噬外段(OS)。采用冷冻切片免疫荧光法检测小胶质细胞吞噬标志物的表达。采用TUNEL法和苏木精、伊红染色法测定PR存活率。通过12例患者中央凹中心的光学相干断层扫描(OCT),观察RD后OS的临床特征。结果:RD后OS经历了一个积累-清除过程,变形虫小胶质细胞在SRS内积累并吞噬OS。在视网膜下小胶质细胞中观察到吞噬标志物的上调。在一些RD患者中,小胶质细胞的消耗导致OS清除失败和视网膜皱褶,这与视网膜外波动(ORU)具有相同的特征。PR没有从小胶质细胞的消耗中获益,因为长期观察到PR的形态和厚度没有恢复。结论:这些结果表明,小胶质细胞吞噬OS是RD后的一个关键过程,吞噬不足导致OS在SRS和PR异常中积累。适当调节小胶质细胞吞噬去除OS可能是调节光感受器存活的新概念。
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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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