Circular RNAs: Potential Star Molecules Involved in Diabetic Retinopathy

2020 ◽  
pp. 1-7
Author(s):  
Miao He ◽  
Rouxi Zhou ◽  
Sen Liu ◽  
Weijing Cheng ◽  
Wei Wang
2021 ◽  
Vol 8 ◽  
Author(s):  
Jianjin Guo ◽  
Feng Xiao ◽  
Wei Ren ◽  
Yikun Zhu ◽  
Qiujing Du ◽  
...  

Background: Increasing attention has been attracted by the role of circular RNAs (circRNAs) in ocular diseases. Previous study has revealed that circ_0005941 (also known as circFTO, an alpha-ketoglutarate–dependent dioxygenase) was upregulated in the vitreous humor of diabetic retinopathy (DR), while its underlying mechanism in DR remains unknown.Methods: Retinal vascular endothelial cells (RVECs) treated with high glucose (HG) were used to establish the DR cell model. The in vivo assays were conducted using streptozotocin-induced diabetic mice. The circular structure and stability of circFTO were identified by Sanger sequencing and RNase R treatment. RT-qPCR analysis was used to detect the RNA expression. The levels of the mRNA-encoded protein thioredoxin-interacting protein (TXNIP) or angiogenesis-associated proteins (VEGFA, PDGF, and ANG2) and blood–retinal barrier (BRB)-related proteins (ZO-1, Occludin, and Claudin-5) were measured by Western blot. The viability of RVECs was measured using CCK-8 assays. The angiogenesis of RVECs was assessed using tube formation assays in vitro. Endothelial permeability assays were conducted to examine the function of the BRB. The binding between genes was explored using RNA pulldown and luciferase reporter assays.Results: CircFTO was upregulated in HG-treated RVECs. CircFTO deficiency reversed the HG-induced increase in the viability and angiogenesis of RVECs and alleviated HG-mediated impairment of the BRB. MiR-128-3p bound with circFTO and was downregulated in HG-treated RVECs. TXNIP was a downstream target gene of miR-128-3p. TXNIP was highly expressed in the DR cell model. Rescue assays revealed that circFTO promoted angiogenesis and impaired the blood–retinal barrier by upregulating TXNIP. In the DR mouse model, circFTO silencing inhibited angiogenesis and promoted BRB recovery in vivo.Conclusion: CircFTO promotes angiogenesis and impairs the blood–retinal barrier in vitro and in vivo by binding with miR-128-3p to upregulate TXNIP in DR.


2017 ◽  
Vol 58 (3) ◽  
pp. 176-184 ◽  
Author(s):  
Yonghao Gu ◽  
Genjie Ke ◽  
Lin Wang ◽  
Enliang Zhou ◽  
Kai Zhu ◽  
...  

2020 ◽  
Author(s):  
Miao He ◽  
Rouxi Zhou ◽  
Sen Liu ◽  
Weijing Cheng ◽  
Wei Wang

ABSTRACTCircular RNAs (CircRNAs) are endogenous long non-coding RNAs. Unlike linear RNAs, they are structurally continuous and covalently closed, without 5 ’caps or 3’ polyadenylation tails. High-throughput RNA sequencing has enabled people to find several endogenous circRNAs in different species and tissues. circRNA mainly acts as a sponge for microRNAs in cytoplasm to regulates protein translation, or interacts with RNA-binding proteins to generate RNA protein complexes that control transcription. circRNAs are closely associated with diseases such as diabetes, neurological disorders, cardiovascular diseases and cancer, which indicates that circRNAs are closely related to and also play an important functional role in the occurrence and development of human diseases. Recent studies have shown that they are differentially expressed in healthy and diseased eye tissues. There lacks of biomarkers for early detection of diabetic retinopathy, and the newly discovered circRNAs seem to be an ideal candidate of novel molecular markers and therapeutic targets. However, the molecular mechanism of circRNAs activity in the occurrence and development of diabetic retinopathy are not clear yet. This systematic review aims to summarize the research status on function and mechanism of circRNAs in regulating the occurrence of diabetic retinopathy.


2019 ◽  
Vol 70 ◽  
pp. 141-152 ◽  
Author(s):  
Jianhong Liu ◽  
Dongpei Li ◽  
Hui Luo ◽  
Xiao Zhu
Keyword(s):  

Genomics ◽  
2021 ◽  
Vol 113 (1) ◽  
pp. 356-365
Author(s):  
HARON Salih ◽  
Xiao Wang ◽  
Baojun Chen ◽  
Yinhua Jia ◽  
Wenfang Gong ◽  
...  

2011 ◽  
Vol 44 (13) ◽  
pp. 59
Author(s):  
SHERRY BOSCHERT
Keyword(s):  

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