摘要
糖尿病视网膜病变(DR)是造成处于工作年龄的成年人失明的主要原因。人类糖尿病视网膜病变的特点是基底膜变厚,周细胞丧失,微动脉瘤形成,视网膜血管新生和晶状体出血。为了探讨在糖尿病视网膜病变中UPP是否激活ROS / PARP和NF-κB炎症因子通路,利用人类视网膜血管内皮细胞 (HRECs)和链脲佐菌素诱导糖尿病的大鼠,通过流式细胞仪检测,免疫组织化学、实时荧光定量PCR,蛋白质印迹分析及酶联免疫吸附试验来确定UPP对ROS的产生、细胞凋亡、线粒体膜电位(ΔΨm)和炎症因子蛋白表达的影响。高糖诱导糖尿病的HRECs和糖尿病大鼠视网膜细胞中,ROS和细胞凋亡水平、UPP (Ub 和E3)和炎症因子蛋白的表达均有所升高,而ΔΨm却有所降低。通过抑制ROS / PARP通路和NF-κB炎症因子的表达,UPP抑制剂和 UbshRNA可以减弱这些影响。而UPP的增加是由于高糖诱导的ROS产生和NF-κBp65表达的增加以及ΔΨm的降低所引起。临床研究证实了增殖性DR(PDR)患者中UPP的过度表达和视网膜前膜的剥离。研究表明,UPP对DR的致病作用与ROS 产生增加以及 NF-κB 的表达有关,这与ROS/PARP 和 NF-κB 炎症因子通路相关。本文对UPP抑制剂治疗DR的进一步应用提供了新的视角。
关键词: 糖尿病视网膜病变,ERMs
Current Molecular Medicine
Title:UPP mediated Diabetic Retinopathy via ROS/PARP and NF-κB inflammatory factor pathways.
Volume: 15 Issue: 8
Author(s): D. -W . Luo, Z. Zheng, H. Wang, Y. Fan, F. Chen, Y. Sun, W. -J. Wang, T. Sun and X. Xu
Affiliation:
关键词: 糖尿病视网膜病变,ERMs
摘要: Diabetic retinopathy (DR) is a leading cause of blindness in adults at working age. Human diabetic retinopathy is characterized by the basement membrane thick, pericytes loss, microaneurysms formation, retina neovascularization and vitreous hemorrhage. To investigate whether UPP activated ROS/PARP and NF-κB inflammatory factor pathways in Diabetic Retinopathy, human retinal endothelial cells (HRECs) and rats with streptozotocin-induced diabetes were used to determine the effect of UPP on ROS generation, cell apoptosis, mitochondrial membrane potential (ΔΨm) and inflammatory factor protein expression, through flow cytometry assay, immunohistochemistry, Real-time PCR, Western blot analysis and ELISA. The levels of ROS and apoptosis and the expressions of UPP (Ub and E3) and inflammatory factor protein were increased in high glucose-induced HRECs and retina of diabetic rats, while ΔΨm was decreased. The UPP inhibitor and UbshRNA could attenuate these effects through inhibiting the pathway of ROS/PARP and the expression of NF-κB inflammatory factors, and the increased UPP was a result of high glucose-induced increase of ROS generation and NF-κBp65 expression, accompanied with the decrease of ΔΨm. Clinical study showed the overexpression of UPP and detachment of epiretinal membranes in proliferative DR (PDR) patients. It has been indicated that the pathogenic effect of UPP on DR was involved in the increase of ROS generation and NF-κB expression, which associated with the ROS/PARP and NF-κB inflammatory factor pathways. Our study supports a new insight for further application of UPP inhibitor in DR treatment.
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D. -W . Luo, Z. Zheng, H. Wang, Y. Fan, F. Chen, Y. Sun, W. -J. Wang, T. Sun and X. Xu , UPP mediated Diabetic Retinopathy via ROS/PARP and NF-κB inflammatory factor pathways., Current Molecular Medicine 2015; 15 (8) . https://dx.doi.org/10.2174/1566524015666150921110500
DOI https://dx.doi.org/10.2174/1566524015666150921110500 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
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