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miRNA-301a-3p 通过调节六跨膜上皮抗原 4 促进糖尿病视网膜病变。

MicroRNA-301a-3p promotes diabetic retinopathy via regulation of six-transmembrane epithelial antigen of prostate 4.

机构信息

Department of Nursing, Xingtai Medical College, Hebei, 054000, China.

Department of Clinical, Xingtai Medical College, Hebei, 054000, China.

出版信息

Inflamm Res. 2021 Apr;70(4):445-457. doi: 10.1007/s00011-020-01431-0. Epub 2021 Feb 20.

DOI:10.1007/s00011-020-01431-0
PMID:33609142
Abstract

OBJECTIVE AND DESIGN

Diabetic retinopathy (DR) is one of the most serious microvascular complications of diabetes mellitus (DM). MicroRNAs (miRNAs) have been discovered to play a crucial role in DR, but the mechanisms underlying the effects of miR-301a-3p on DR are poorly understood. This paper was designed to explore the possible role of miR-301a-3p in DR.

METHODS

The diabetic rat model was established by a single intraperitoneal injection of streptozotocin (STZ). The effects of miR-301a-3p on the biological functions of HRECs were determined through a series of experiments in vitro/vivo.

RESULTS

The results revealed that interference with miR-301a-3p could decrease the expressions of inflammatory factors and apoptosis in the retinal tissue of DR. Furthermore, it can alleviate the oxidative stress in DR serum, reduce VEGF expression, increase endothelial cell marker expression, and inhibit (High Glucose) HG-induced apoptosis of HRECs. Six-transmembrane epithelial antigen of prostate 4 (STEAP4) was the target of miR-301a-3p. All the effects of miR-301a-3p in DR model were reversed by STEAP4 inhibitor.

CONCLUSION

miR-301a-3p promotes diabetic retinopathy via regulation of STEAP4. The findings in this study may provide a vital reference for the drug research and development in DR treatment.

摘要

目的和设计

糖尿病视网膜病变(DR)是糖尿病(DM)最严重的微血管并发症之一。现已发现 microRNAs(miRNAs)在 DR 中发挥着关键作用,但 miR-301a-3p 对 DR 影响的机制尚不清楚。本文旨在探讨 miR-301a-3p 在 DR 中的可能作用。

方法

通过单次腹腔注射链脲佐菌素(STZ)建立糖尿病大鼠模型。通过一系列体外/体内实验确定 miR-301a-3p 对 HRECs 生物学功能的影响。

结果

结果表明,干扰 miR-301a-3p 可降低 DR 视网膜组织中炎症因子和细胞凋亡的表达。此外,它可以减轻 DR 血清中的氧化应激,降低 VEGF 表达,增加内皮细胞标志物表达,并抑制(高葡萄糖)HG 诱导的 HRECs 凋亡。六跨膜上皮抗原 4(STEAP4)是 miR-301a-3p 的靶标。miR-301a-3p 在 DR 模型中的所有作用均被 STEAP4 抑制剂逆转。

结论

miR-301a-3p 通过调节 STEAP4 促进糖尿病视网膜病变。本研究的结果可为 DR 治疗的药物研究和开发提供重要参考。

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本文引用的文献

1
Effect of intravitreal conbercept treatment before vitrectomy in proliferative diabetic retinopathy.玻璃体切割术前玻璃体内注射康柏西普治疗增生性糖尿病视网膜病变的效果
Int J Ophthalmol. 2018 Jul 18;11(7):1217-1221. doi: 10.18240/ijo.2018.07.23. eCollection 2018.
2
Downregulation of miR-301a-3p sensitizes pancreatic cancer cells to gemcitabine treatment via PTEN.miR-301a-3p的下调通过PTEN使胰腺癌细胞对吉西他滨治疗敏感。
Am J Transl Res. 2017 Apr 15;9(4):1886-1895. eCollection 2017.
3
Diabetes and retinal vascular dysfunction.糖尿病与视网膜血管功能障碍。
氧化应激在糖尿病性血管内皮功能障碍中的作用。
Cardiovasc Diabetol. 2023 Sep 2;22(1):237. doi: 10.1186/s12933-023-01965-7.
4
Oxidative Stress and Its Regulation in Diabetic Retinopathy.氧化应激及其在糖尿病视网膜病变中的调节
Antioxidants (Basel). 2023 Aug 21;12(8):1649. doi: 10.3390/antiox12081649.
5
Noncoding RNAs Are Promising Therapeutic Targets for Diabetic Retinopathy: An Updated Review (2017-2022).非编码 RNA 是糖尿病视网膜病变有希望的治疗靶点:最新综述 (2017-2022)。
Biomolecules. 2022 Nov 28;12(12):1774. doi: 10.3390/biom12121774.
J Ophthalmic Vis Res. 2014 Jul-Sep;9(3):362-73. doi: 10.4103/2008-322X.143378.
4
Effects of VEGFR-1, VEGFR-2, and IGF-IR hammerhead ribozymes on glucose-mediated tight junction expression in cultured human retinal endothelial cells.血管内皮生长因子受体-1(VEGFR-1)、血管内皮生长因子受体-2(VEGFR-2)和胰岛素样生长因子受体-1(IGF-IR)锤头状核酶对培养的人视网膜内皮细胞中葡萄糖介导的紧密连接表达的影响。
Mol Vis. 2006 Jan 12;12:32-42.
5
VEGF-initiated blood-retinal barrier breakdown in early diabetes.糖尿病早期血管内皮生长因子引发的血视网膜屏障破坏
Invest Ophthalmol Vis Sci. 2001 Sep;42(10):2408-13.