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Exosomal miRNA Profiling in Vitreous Humor in Proliferative Diabetic Retinopathy

MicroRNAs (miRNAs) are small noncoding RNAs which mediate some of the pathological mechanisms of diabetic retinopathy. The aim of this study was to identify differentially expressed miRNAs in the vitreal exosomes of proliferative diabetic retinopathy (PDR) patients and non-diabetic controls. Exosome...

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Autores principales: Kot, Agnieszka, Kaczmarek, Radoslaw
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818905/
https://www.ncbi.nlm.nih.gov/pubmed/36611916
http://dx.doi.org/10.3390/cells12010123
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author Kot, Agnieszka
Kaczmarek, Radoslaw
author_facet Kot, Agnieszka
Kaczmarek, Radoslaw
author_sort Kot, Agnieszka
collection PubMed
description MicroRNAs (miRNAs) are small noncoding RNAs which mediate some of the pathological mechanisms of diabetic retinopathy. The aim of this study was to identify differentially expressed miRNAs in the vitreal exosomes of proliferative diabetic retinopathy (PDR) patients and non-diabetic controls. Exosomes were extracted from the vitreous samples of 10 PDR patients and 10 controls. The expression of 372 miRNAs was determined using a quantitative polymerase chain reaction (qPCR) panel. We have demonstrated a significant dysregulation in 26 miRNAs. The most remarkable findings include a profound attenuation of the miR-125 family, as well as enhanced miR-21-5p expression in the diabetic samples. We also showed the downregulation of miR-204-5p and the upregulation of let-7g in PDR compared to the controls. This study identified miR-125 and miR-21 as potential targets for further functional analysis regarding their putative role in the pathogenesis of PDR.
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spelling pubmed-98189052023-01-07 Exosomal miRNA Profiling in Vitreous Humor in Proliferative Diabetic Retinopathy Kot, Agnieszka Kaczmarek, Radoslaw Cells Article MicroRNAs (miRNAs) are small noncoding RNAs which mediate some of the pathological mechanisms of diabetic retinopathy. The aim of this study was to identify differentially expressed miRNAs in the vitreal exosomes of proliferative diabetic retinopathy (PDR) patients and non-diabetic controls. Exosomes were extracted from the vitreous samples of 10 PDR patients and 10 controls. The expression of 372 miRNAs was determined using a quantitative polymerase chain reaction (qPCR) panel. We have demonstrated a significant dysregulation in 26 miRNAs. The most remarkable findings include a profound attenuation of the miR-125 family, as well as enhanced miR-21-5p expression in the diabetic samples. We also showed the downregulation of miR-204-5p and the upregulation of let-7g in PDR compared to the controls. This study identified miR-125 and miR-21 as potential targets for further functional analysis regarding their putative role in the pathogenesis of PDR. MDPI 2022-12-28 /pmc/articles/PMC9818905/ /pubmed/36611916 http://dx.doi.org/10.3390/cells12010123 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kot, Agnieszka
Kaczmarek, Radoslaw
Exosomal miRNA Profiling in Vitreous Humor in Proliferative Diabetic Retinopathy
title Exosomal miRNA Profiling in Vitreous Humor in Proliferative Diabetic Retinopathy
title_full Exosomal miRNA Profiling in Vitreous Humor in Proliferative Diabetic Retinopathy
title_fullStr Exosomal miRNA Profiling in Vitreous Humor in Proliferative Diabetic Retinopathy
title_full_unstemmed Exosomal miRNA Profiling in Vitreous Humor in Proliferative Diabetic Retinopathy
title_short Exosomal miRNA Profiling in Vitreous Humor in Proliferative Diabetic Retinopathy
title_sort exosomal mirna profiling in vitreous humor in proliferative diabetic retinopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818905/
https://www.ncbi.nlm.nih.gov/pubmed/36611916
http://dx.doi.org/10.3390/cells12010123
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