The Long Non-Coding RNA HOTAIR Is a Critical Epigenetic Mediator of Angiogenesis in Diabetic Retinopathy

被引:59
作者
Biswas, Saumik [1 ]
Feng, Biao [1 ]
Chen, Shali [1 ]
Liu, Jieting [1 ]
Aref-Eshghi, Erfan [1 ]
Gonder, John [2 ]
Ngo, Vy [1 ]
Sadikovic, Bekim [1 ]
Chakrabarti, Subrata [1 ]
机构
[1] Western Univ, Dept Pathol & Lab Med, DSB 4033,1151 Richmond St, London, ON N6A 5C1, Canada
[2] Western Univ, Dept Ophthalmol, London, ON, Canada
基金
加拿大健康研究院;
关键词
LncRNA; HOTAIR; epigenetics; angiogenesis; diabetic retinopathy;
D O I
10.1167/iovs.62.3.20
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. Diabetic retinopathy (DR) remains a pressing issue worldwide. Abnormal angiogenesis is a distinct vascular lesion in DR, and research has established that vascular endothelial growth factor A (VEGF-A) is a primary mediator of such changes. However, limitations in current anti-VEGF therapies suggest that our understanding of molecular networks underlying ocular angiogenesis remains far from complete. Based on our long non-coding RNA (lncRNA) array analyses, HOX antisense intergenic RNA (HOTAIR) was identified as one of the top upregulated lncRNAs in high glucose-cultured human retinal endothelial cells (HRECs). Given the well-documented roles of HOTAIR in cancer, no studies have examined the epigenetic implications of HOTAIR in DR, and we investigated such relationships herein. METHODS. We used HRECs exposed to various glucose concentrations and epigenetic modulators to examine HOTAIR, angiogenic, and DR-related molecular markers. Oxidative stress, angiogenesis, and mitochondrial dysfunction were assessed. Retinal tissues of diabetic rodents and the vitreous humor and serum of patients with proliferative DR were also investigated. RESULTS. Hyperglycemia significantly augmented HOTAIR expression in HRECs and promoted angiogenesis, oxidative damage, and mitochondrial aberrations. Similarly, vitreous humor and serum from proliferative DR patients and retinas from diabetic animals demonstrated increased HOTAIR expression compared to non-diabetic controls. HOTAIR knockdown protected against glucose-induced increases of angiogenic and diabetesassociated molecules in the retina. Mechanistically, we showed that HOTAIR exerts its capabilities by preventing oxidative stress and modulating epigenetic pathways involving histone methylation, histone acetylation, DNA methylation, and transcription factors. CONCLUSIONS. Our findings suggest that HOTAIR is a critical lncRNA in the pathogenesis of DR and may potentially be important for diagnostic and therapeutic targeting.
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页数:12
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