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自噬调节剂对氧诱导视网膜病变小鼠模型中血管、神经胶质和神经元改变的影响。

Effect of Autophagy Modulators on Vascular, Glial, and Neuronal Alterations in the Oxygen-Induced Retinopathy Mouse Model.

作者信息

Subirada Paula V, Paz María C, Ridano Magali E, Lorenc Valeria E, Fader Claudio M, Chiabrando Gustavo A, Sánchez María C

机构信息

Departamento de Bioquímica Clínica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, Argentina.

Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Centro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI), Córdoba, Argentina.

出版信息

Front Cell Neurosci. 2019 Jun 26;13:279. doi: 10.3389/fncel.2019.00279. eCollection 2019.

Abstract

Hypoxia is one of the main insults in proliferative retinopathies, leading to neovascularization and neurodegeneration. To maintain homeostasis, neurons require efficient degradation and recycling systems. Autophagy participates in retinal cell death, but it is also a cell survival mechanism. Here, we analyzed the role of autophagy at the three characteristic time periods in the oxygen-induced retinopathy (OIR) mouse model and determined if its modulation can improve vascular and non-vascular alterations. Experiments were performed with chloroquine (CQ) in order to monitor autophagosome accumulation by lysosomal blockade. Post natal day (P)17 OIR mouse retinas showed a significant increase in autophagy flux. In particular, an intense LC3B and p62 staining was observed in inner layers of the retina, mainly proliferating endothelial cells. After a single intraocular injection of Rapamycin at P12 OIR, a decreased neovascular area and vascular endothelial growth factor (VEGF) protein expression were observed at P17 OIR. In addition, whereas the increased expression of glial fibrillary acidic protein (GFAP) was reversed at P26 OIR, the functional alterations persisted. Using a similar therapeutic schedule, we analyzed the effect of anti-VEGF therapy on autophagy flux. Like Rapamycin, VEGF inhibitor treatment not only reduced the amount of neovascular tufts, but also activated autophagy flux at P17 OIR, mainly in ganglion cell layer and inner nuclear layer. Finally, the effects of the disruption of autophagy by Spautin-1, were evaluated at vascular, glial, and neuronal levels. After a single dose of Spautin-1, Western blot analysis showed a significant decrease in LC3B II and p62 protein expression at P13 OIR, returning both autophagy markers to OIR control levels at P17. In addition, neither gliosis nor functional alterations were attenuated. In line with these results, TUNEL staining showed a slight increase in the number of positive cells in the outer nuclear layer at P17 OIR. Overall, our results demonstrate that all treatments of induction or inhibition of the autophagic flux reduced neovascular area but were unable to completely reverse the neuronal damage. Besides, compared to current treatments, rapamycin provides a more promising therapeutic strategy as it reduces both neovascular tufts and persistent gliosis.

摘要

缺氧是增殖性视网膜病变的主要损伤因素之一,可导致新生血管形成和神经退行性变。为维持体内平衡,神经元需要高效的降解和循环系统。自噬参与视网膜细胞死亡,但它也是一种细胞存活机制。在此,我们分析了自噬在氧诱导性视网膜病变(OIR)小鼠模型三个特征时间段中的作用,并确定其调节是否能改善血管和非血管改变。使用氯喹(CQ)进行实验,以通过溶酶体阻断监测自噬体积累。出生后第(P)17天的OIR小鼠视网膜显示出自噬通量显著增加。特别是,在视网膜内层,主要是增殖的内皮细胞中观察到强烈的LC3B和p62染色。在P12 OIR时单次眼内注射雷帕霉素后,在P17 OIR时观察到新生血管面积减少和血管内皮生长因子(VEGF)蛋白表达降低。此外,虽然在P26 OIR时胶质纤维酸性蛋白(GFAP)表达增加的情况得到逆转,但功能改变仍然存在。使用类似的治疗方案,我们分析了抗VEGF治疗对自噬通量的影响。与雷帕霉素一样,VEGF抑制剂治疗不仅减少了新生血管丛的数量,还在P17 OIR时激活了自噬通量,主要在神经节细胞层和内核层。最后,在血管、胶质细胞和神经元水平评估了Spautin-1破坏自噬的作用。单次注射Spautin-1后,蛋白质印迹分析显示在P13 OIR时LC3B II和p62蛋白表达显著降低,在P17时两种自噬标志物均恢复到OIR对照水平。此外,神经胶质增生和功能改变均未减轻。与这些结果一致,TUNEL染色显示在P17 OIR时外核层阳性细胞数量略有增加。总体而言,我们的结果表明,所有诱导或抑制自噬通量的治疗均减少了新生血管面积,但无法完全逆转神经元损伤。此外,与目前的治疗相比,雷帕霉素提供了一种更有前景的治疗策略,因为它既能减少新生血管丛,又能减轻持续性神经胶质增生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c4/6608561/b36c90fd9138/fncel-13-00279-g001.jpg

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