» Articles » PMID: 36009007

The Protective Effects of Neurotrophins and MicroRNA in Diabetic Retinopathy, Nephropathy and Heart Failure Via Regulating Endothelial Function

Overview
Journal Biomolecules
Publisher MDPI
Date 2022 Aug 26
PMID 36009007
Authors
Affiliations
Soon will be listed here.
Abstract

Diabetes mellitus is a common disease affecting more than 537 million adults worldwide. The microvascular complications that occur during the course of the disease are widespread and affect a variety of organ systems in the body. Diabetic retinopathy is one of the most common long-term complications, which include, amongst others, endothelial dysfunction, and thus, alterations in the blood-retinal barrier (BRB). This particularly restrictive physiological barrier is important for maintaining the neuroretina as a privileged site in the body by controlling the inflow and outflow of fluid, nutrients, metabolic end products, ions, and proteins. In addition, people with diabetic retinopathy (DR) have been shown to be at increased risk for systemic vascular complications, including subclinical and clinical stroke, coronary heart disease, heart failure, and nephropathy. DR is, therefore, considered an independent predictor of heart failure. In the present review, the effects of diabetes on the retina, heart, and kidneys are described. In addition, a putative common microRNA signature in diabetic retinopathy, nephropathy, and heart failure is discussed, which may be used in the future as a biomarker to better monitor disease progression. Finally, the use of miRNA, targeted neurotrophin delivery, and nanoparticles as novel therapeutic strategies is highlighted.

Citing Articles

Tissue origin of endothelial cells determines immune system modulation and regulation of HIF-1α-, TGF-β-, and VEGF signaling.

Heiden R, Hannig L, Bernhard J, Vallon M, Schlecht A, Hofmann N iScience. 2025; 28(2):111740.

PMID: 39925414 PMC: 11804623. DOI: 10.1016/j.isci.2024.111740.


Effects of mesenchymal stromal cells and human recombinant Nerve Growth Factor delivered by bioengineered human corneal lenticule on an innovative model of diabetic retinopathy.

Pelusi L, Hurst J, Detta N, Pipino C, Lamolinara A, Conte G Front Endocrinol (Lausanne). 2024; 15:1462043.

PMID: 39473506 PMC: 11518713. DOI: 10.3389/fendo.2024.1462043.


The application and clinical translation of the self-evolving machine learning methods in predicting diabetic retinopathy and visualizing clinical transformation.

Li B, Hu L, Zhang S, Li S, Tang W, Chen G Front Endocrinol (Lausanne). 2024; 15:1429974.

PMID: 39363895 PMC: 11446766. DOI: 10.3389/fendo.2024.1429974.


Synergistic Effects of Weight Loss and Catheter Ablation: Can microRNAs Serve as Predictive Biomarkers for the Prevention of Atrial Fibrillation Recurrence?.

Forster C, Kunzel S, Shityakov S, Stavrakis S Int J Mol Sci. 2024; 25(9).

PMID: 38731908 PMC: 11083177. DOI: 10.3390/ijms25094689.


Serum VEGF, high-sensitivity CRP, and cystatin-C assist in the diagnosis of type 2 diabetic retinopathy complicated with hyperuricemia.

Wei J, Zhang J, Shi Y, Zhang H, Wu Y Open Med (Wars). 2023; 18(1):20230857.

PMID: 38075033 PMC: 10710213. DOI: 10.1515/med-2023-0857.


References
1.
Nico B, Mangieri D, Benagiano V, Crivellato E, Ribatti D . Nerve growth factor as an angiogenic factor. Microvasc Res. 2007; 75(2):135-41. DOI: 10.1016/j.mvr.2007.07.004. View

2.
COGAN D, Toussaint D, Kuwabara T . Retinal vascular patterns. IV. Diabetic retinopathy. Arch Ophthalmol. 1961; 66:366-78. DOI: 10.1001/archopht.1961.00960010368014. View

3.
Tang J, Kern T . Inflammation in diabetic retinopathy. Prog Retin Eye Res. 2011; 30(5):343-58. PMC: 3433044. DOI: 10.1016/j.preteyeres.2011.05.002. View

4.
Winer D, Winer S, Shen L, Wadia P, Yantha J, Paltser G . B cells promote insulin resistance through modulation of T cells and production of pathogenic IgG antibodies. Nat Med. 2011; 17(5):610-7. PMC: 3270885. DOI: 10.1038/nm.2353. View

5.
Skaper S . Neurotrophic Factors: An Overview. Methods Mol Biol. 2017; 1727:1-17. DOI: 10.1007/978-1-4939-7571-6_1. View