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Now published in The Lancet

Downregulation of circRNA DMNT3B Contributes to Diabetic Retinal Vascular Dysfunction Through Targeting miR-20b-5p and BAMBI

34 Pages Posted: 13 Sep 2019

See all articles by Ke Zhu

Ke Zhu

Fudan University - Department of Ophthalmology and Optometry

Xin Hu

Fudan University - Department of Neurology

Han Chen

Fudan University - Department of Ophthalmology and Optometry

Fang Li

Fudan University - Department of Neurology

Ning Yin

Fudan University - Department of Neurology

Ai-Lin Liu

Fudan University - Department of Neurology

Kun Shan

Fudan University - Department of Ophthalmology and Optometry

Yao-Wu Qin

Fudan University - Department of Ophthalmology and Optometry

Xin Huang

Fudan University - Department of Neurology

Qing Chang

Fudan University - Department of Ophthalmology and Optometry

Ge-Zhi Xu

Fudan University - Department of Ophthalmology and Optometry

Zhongfeng Wang

Fudan University - Department of Neurology

More...

Abstract

Background: Diabetic retinopathy, a vascular complication of diabetes mellitus, is the leading cause of visual impairment and blindness. circRNAs act as competing endogenous RNA, sponging target miRNA and thus influencing mRNA expression in vascular diseases. We investigated whether and how circDNMT3B is involved in retinal vascular dysfunction under diabetic conditions.

Methods: qRT-PCR was performed to detect expression of circDNMT3B, miR-20b-5p, and BAMBI in retinal microvascular endothelial cells under diabetic conditions. Western blot, Cell Counting Kit-8, Transwell, Matrigel tube formation, and retinal trypsin digestion assays were conducted to explore the roles of circDNMT3B/miR-20b-5p/BAMBI in retinal vascular dysfunction. Bioinformatics analysis and luciferase reporter, siRNA, and overexpression assays were used to reveal the mechanisms of the circDNMT3B/miR-20b-5p/BAMBI interaction. Electroretinograms were used to evaluate visual function.

Findings: Upregulation of miR-20b-5p under diabetic conditions promoted proliferation, migration, and tube formation of human retinal microvascular endothelial cells (HRMECs), which was mediated by downregulated BAMBI. Under diabetic conditions, circDNMT3B, which acts as a sponge of miR-20b-5p, is downregulated. circDNMT3B overexpression reduced retinal acellular capillary number and alleviated visual damage in diabetic rats. Changes in expression of circDNMT3B and miR-20b-5p were confirmed in the proliferative fibrovascular membranes of patients with diabetic retinopathy.

Interpretation: Downregulation of circDNMT3B contributes to vascular dysfunction in diabetic retinas through regulating miR-20b-5p and BAMBI, providing a potential treatment strategy for diabetic retinopathy.

Funding Statement: This work was supported by the National Natural Science Foundation of China (No. 81790642, 31800872, 81570854, and 81770944), the National Key Basic Research Program of China (2013CB967503), the Shanghai Municipal Science and Technology Major Project (No.2018SHZDZX01) and ZJLab.

Declaration of Interests: All authors declare no conflict interests.

Ethics Approval Statement: All procedures were explained to patients, and informed consent was provided.

All procedures met the ethical standards of the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research and the guidelines of Fudan University.

This study was approved by the Institutional Ethics Review Committee of the Eye & ENT Hospital of Fudan University.

Keywords: Diabetic retinopathy; retinal microvascular endothelial cells; circDNMT3B; miR-20b-5p; BAMBI

Suggested Citation

Zhu, Ke and Hu, Xin and Chen, Han and Li, Fang and Yin, Ning and Liu, Ai-Lin and Shan, Kun and Qin, Yao-Wu and Huang, Xin and Chang, Qing and Xu, Ge-Zhi and Wang, Zhongfeng, Downregulation of circRNA DMNT3B Contributes to Diabetic Retinal Vascular Dysfunction Through Targeting miR-20b-5p and BAMBI (March 9, 2019). Available at SSRN: https://ssrn.com/abstract=3449319 or http://dx.doi.org/10.2139/ssrn.3449319

Ke Zhu

Fudan University - Department of Ophthalmology and Optometry

Shanghai, 200031
China

Xin Hu

Fudan University - Department of Neurology

138 Yixueyuan Road
Shanghai, 200032
China

Han Chen

Fudan University - Department of Ophthalmology and Optometry

Shanghai, 200031
China

Fang Li

Fudan University - Department of Neurology

138 Yixueyuan Road
Shanghai, 200032
China

Ning Yin

Fudan University - Department of Neurology

138 Yixueyuan Road
Shanghai, 200032
China

Ai-Lin Liu

Fudan University - Department of Neurology

138 Yixueyuan Road
Shanghai, 200032
China

Kun Shan

Fudan University - Department of Ophthalmology and Optometry

Shanghai, 200031
China

Yao-Wu Qin

Fudan University - Department of Ophthalmology and Optometry

Shanghai, 200031
China

Xin Huang

Fudan University - Department of Neurology

138 Yixueyuan Road
Shanghai, 200032
China

Qing Chang

Fudan University - Department of Ophthalmology and Optometry

Shanghai, 200031
China

Ge-Zhi Xu

Fudan University - Department of Ophthalmology and Optometry ( email )

Shanghai, 200031
China

Zhongfeng Wang (Contact Author)

Fudan University - Department of Neurology ( email )

138 Yixueyuan Road
Shanghai, 200032
China