Skip to main content
Top
Published in: Acta Diabetologica 12/2020

01-12-2020 | Diabetic Retinopathy | Original Article

MicroRNA-148a-3p alleviates high glucose-induced diabetic retinopathy by targeting TGFB2 and FGF2

Authors: Jihong Wang, Yong Yao, Kelei Wang, Jia Li, Ting Chu, Haicui Shen

Published in: Acta Diabetologica | Issue 12/2020

Login to get access

Abstract

Aims

Diabetic retinopathy (DR), a common complication of type 1 or type 2 diabetes mellitus, has become the leading cause of blindness among adults in working age. The dysregulation of microRNA has been reported to be strongly related to the initiation or progression of DR. However, neither the biological role nor the molecular mechanism of miR-148a-3p has been researched in DR. This study is designed to investigate the function and mechanism of miR-148a-3p in DR.

Methods

The bioinformatics analysis (Targetscan: https://​www.​targetscan.​org/​vert_​72/​) and numerous experiments including real-time quantitative polymerase chain reaction, terminal deoxynucleotidyltransferase dUTP nick end labeling, CCK-8, western blot, vasculogenesis and luciferase reporter assays were used to research the function and mechanism of miR-148a-3p in DR.

Results

We constructed DR cell model by treating human retinal microvascular endothelial cells (HRECs) with different concentration gradients of high glucose (HG). Additionally, HG treatment reduced miR-148a-3p level in HRECs. In function, overexpression of miR-148a-3p caused an increase in cell viability and a decrease in cell apoptosis. Besides, miR-148a-3p overexpression led to a damage on blood–retinal barrier (BRB) and suppressed angiogenesis. In mechanism, miR-148a-3p specifically bound to 3′ untranslated region of TGFB2 and FGF2. At least, rescue assays demonstrated that the inhibitive influence of miR-148a-3p mimics on BRB injury was offset by overexpression of TGFB2 and the attenuation of angiogenesis resulting from miR-148a-3p mimics was abrogated by overexpression of FGF2

Conclusions

In a word, we discovered that miR-148a-3p alleviated HG-induced DR by targeting TGFB2 and FGF2. This novel discovery indicated miR-148a-3p as a potential target for DR diagnosis or treatment.
Literature
4.
go back to reference Sosna T (2016) History of diagnosis and therapy of diabetic retinopathy. Vnitr Lek 62(11 Suppl 4):S136–S141PubMed Sosna T (2016) History of diagnosis and therapy of diabetic retinopathy. Vnitr Lek 62(11 Suppl 4):S136–S141PubMed
5.
go back to reference Pelikanova T (2016) Diabetic retinopathy: pathogenesis and therapeutic implications. Vnitrni Lek 62(7–8):620–628 Pelikanova T (2016) Diabetic retinopathy: pathogenesis and therapeutic implications. Vnitrni Lek 62(7–8):620–628
12.
go back to reference Peng JS, Chen SY, Wu CL et al (2016) Amelioration of experimental autoimmune arthritis through targeting of synovial fibroblasts by intraarticular delivery of microRNAs 140–3p and 140–5p. Arthritis Rheumatol (Hoboken, NJ) 68(2):370–381. https://doi.org/10.1002/art.39446CrossRef Peng JS, Chen SY, Wu CL et al (2016) Amelioration of experimental autoimmune arthritis through targeting of synovial fibroblasts by intraarticular delivery of microRNAs 140–3p and 140–5p. Arthritis Rheumatol (Hoboken, NJ) 68(2):370–381. https://​doi.​org/​10.​1002/​art.​39446CrossRef
Metadata
Title
MicroRNA-148a-3p alleviates high glucose-induced diabetic retinopathy by targeting TGFB2 and FGF2
Authors
Jihong Wang
Yong Yao
Kelei Wang
Jia Li
Ting Chu
Haicui Shen
Publication date
01-12-2020
Publisher
Springer Milan
Published in
Acta Diabetologica / Issue 12/2020
Print ISSN: 0940-5429
Electronic ISSN: 1432-5233
DOI
https://doi.org/10.1007/s00592-020-01569-7

Other articles of this Issue 12/2020

Acta Diabetologica 12/2020 Go to the issue