Tracking astrocyte polarization in the retina in retinopathy of prematurity

IF 3 2区 医学 Q1 OPHTHALMOLOGY Experimental eye research Pub Date : 2024-11-20 DOI:10.1016/j.exer.2024.110170
Xiaoxiao Feng, Liwei Zhang, Kangwei Jiao, Yunqing Li, Min Wu, Yu Xie, Libo Xiao
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Abstract

Astrocyte patterns affect the normal development of the retinal vascular network in retinopathy of prematurity (ROP), which is associated with VEGF secretion. However, the role of the astrocyte polarization in this process remains unknown. Therefore, this study aimed to track the status of A1/A2 reactive astrocytes in the retinas of the oxygen-induced retinopathy (OIR) model and their association with VEGF expression. The C57BL/6 mouse OIR model was constructed to characterize the pathological changes in ROP. Immunofluorescence of iB4 and GFAP staining was performed to observe changes in the vascular network and astrocyte pattern at different time points (P0, P7, P12, P17, and P21). C3-labeled A1 reactive and S100A10-labeled A2 reactive astrocytes and VEGF were also observed. The pattern of GFAP-labeled astrocyte was altered concurrently with the iB4-positive vascular network during OIR. Astrocyte activity was significantly weakened at P12 and significantly enhanced at P17. Notably, the number of C3-labeled A1 reactive astrocytes was significantly increased at P12, decreased at P17, and normalized at P21 in OIR models. S100A10-labeled A2 reactive astrocytes were significantly increased at P17 but did not change significantly at P12 or P17. VEGF levels were decreased at P7-P12 and increased at P12-P17. The expression pattern of VEGF was opposite to that of C3-labeled A1 reactive astrocytes and identical to that of S100A10-labeled A2 reactive astrocytes. In conclusion, the astrocyte pattern and vascular network exhibited similar changes during the OIR process, and the periods of vaso-obliteration and neo-vascularization display an abnormal activation in A1-and A2-reactive astrocytes.
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跟踪早产儿视网膜病变中视网膜星形胶质细胞的极化。
星形胶质细胞模式会影响早产儿视网膜病变(ROP)视网膜血管网络的正常发育,这与血管内皮生长因子的分泌有关。然而,星形胶质细胞极化在这一过程中的作用仍然未知。因此,本研究旨在追踪氧诱导视网膜病变(OIR)模型视网膜中 A1/A2 反应性星形胶质细胞的状态及其与血管内皮生长因子表达的关系。构建了 C57BL/6 小鼠 OIR 模型来描述 ROP 的病理变化。对 iB4 和 GFAP 进行免疫荧光染色,以观察不同时间点(P0、P7、P12、P17 和 P21)血管网络和星形胶质细胞模式的变化。此外,还观察了 C3 标记的 A1 反应性星形胶质细胞和 S100A10 标记的 A2 反应性星形胶质细胞以及血管内皮生长因子。在 OIR 期间,GFAP 标记的星形胶质细胞模式与 iB4 阳性的血管网络同时发生了改变。星形胶质细胞的活性在 P12 时明显减弱,在 P17 时明显增强。值得注意的是,在 OIR 模型中,C3 标记的 A1 反应性星形胶质细胞的数量在 P12 时明显增加,在 P17 时减少,在 P21 时恢复正常。S100A10标记的A2反应性星形胶质细胞在P17时明显增加,但在P12或P17时没有明显变化。VEGF 水平在 P7-P12 期下降,在 P12-P17 期升高。VEGF 的表达模式与 C3 标记的 A1 反应性星形胶质细胞相反,而与 S100A10 标记的 A2 反应性星形胶质细胞相同。总之,在 OIR 过程中,星形胶质细胞模式和血管网络表现出相似的变化,血管闭塞期和血管新生期显示了 A1 和 A2 反应性星形胶质细胞的异常激活。
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来源期刊
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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