Landscape of microRNA in the aqueous humour of proliferative diabetic retinopathy as assessed by next-generation sequencing

被引:25
|
作者
Chen, Shida [1 ]
Yuan, Miner [1 ]
Liu, Yaoming [1 ]
Zhao, Xiujuan [1 ]
Lian, Ping [1 ]
Chen, Yang [1 ]
Liu, Bingqian [1 ]
Lu, Lin [1 ]
机构
[1] Sun Yat Sen Univ, State Key Lab Ophthalmol, Zhongshan Ophthalm Ctr, 7S Jinsui Rd, Guangzhou 510623, Guangdong, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
biomarker; microRNA; next-generation sequencing; proliferative diabetic retinopathy; piwi-interacting RNA; ANGIOGENIC MICRORNAS; EXPRESSION PROFILES; VITREOUS-HUMOR; SMALL RNAS; EYES; NEURODEGENERATION; BIOMARKERS; BLOOD; CELLS; RISK;
D O I
10.1111/ceo.13554
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background The microRNAs (miRNA) have been found to play an important role in the pathogenesis of diabetic retinopathy. We try to explore the miRNA and piwi-interacting RNA (piRNA) profile in the aqueous humour of proliferative diabetic retinopathy (PDR) using next-generation sequencing (NGS). Methods Aqueous humour samples were collected from nine PDR eyes and nine cataract control eyes, and NGS was performed. Quantitative polymerase chain reaction (qPCR) was used to validate the sequencing results. An oxygen-induced retinopathy (OIR) model was used to validate the angiogenesis related miRNA. Results In total, 484 miRNAs were differently expressed between the PDR eyes and cataract control eyes, including 210 mature miRNAs and 274 novel miRNAs. Furthermore, eight miRNAs and 30 piRNAs were identified as the most differently expressed between the two groups (P > .85). This differential expression of miRNA was predicted to regulate Rho protein signal transduction, neurotransmitter uptake and histone lysine methylation. Relative expression patterns of miR-184, -150-5p and -93-5p were confirmed by qPCR. A reduced expression of miR-93-5p was confirmed in the OIR model. Conclusions This study comprehensively demonstrated the miRNA and piRNA expression profile of the aqueous humour of PDR eyes, which may serve as a potential biomarker and involved in the pathogenesis of PDR.
引用
收藏
页码:925 / 936
页数:12
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