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miRNA Profiling of Circulating Small Extracellular Vesicles From Subarachnoid Hemorrhage Rats Using Next-Generation Sequencing

BACKGROUND: Extracellular vesicles (EVs) are produced during abnormal and normal physiological conditions. Understanding the expression profile of microRNA (miRNA) in plasma-derived small extracellular vesicles (sEVs) and their roles in subarachnoid hemorrhage (SAH) that cause cerebral vasospasm (CV...

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Autores principales: Lan, Shihai, Zhou, Lin, Wang, Yimei, Fang, Linchun, Yang, Le, Zheng, Suyue, Zhou, XinHui, Tang, Bin, Duan, Jian, Wu, Xiao, Yang, Chengxing, Hong, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439219/
https://www.ncbi.nlm.nih.gov/pubmed/32903819
http://dx.doi.org/10.3389/fncel.2020.00242
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author Lan, Shihai
Zhou, Lin
Wang, Yimei
Fang, Linchun
Yang, Le
Zheng, Suyue
Zhou, XinHui
Tang, Bin
Duan, Jian
Wu, Xiao
Yang, Chengxing
Hong, Tao
author_facet Lan, Shihai
Zhou, Lin
Wang, Yimei
Fang, Linchun
Yang, Le
Zheng, Suyue
Zhou, XinHui
Tang, Bin
Duan, Jian
Wu, Xiao
Yang, Chengxing
Hong, Tao
author_sort Lan, Shihai
collection PubMed
description BACKGROUND: Extracellular vesicles (EVs) are produced during abnormal and normal physiological conditions. Understanding the expression profile of microRNA (miRNA) in plasma-derived small extracellular vesicles (sEVs) and their roles in subarachnoid hemorrhage (SAH) that cause cerebral vasospasm (CVS) is imperative. METHODS: Sprague Dawley rats (250–300 g) were allocated to sham or SAH groups established using endovascular perforation method. miRNA expression profiles of plasma sEVs in both groups (each n = 4) were evaluated using next-generation sequencing (NGS). RESULTS: There were 142 microRNAs (miRNAs) significantly expressed differently between the two groups, of which 73 were up-regulated while 69 were down-regulated in SAH sEVs compared with those of sham (p < 0.05; fold change ≥ 2). The Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway and Gene Ontology (GO) analyses of differently expressed (DE) miRNAs revealed signaling pathways and target genes (TGs) in the SAH group. rno-miR-185-5p, rno-miR-103-3p, rno-miR-15b-3p, rno-miR-93-5p, and rno-miR-98-5p were the top five most up-regulated sEVs miRNAs. CONCLUSION: Our results suggest that miRNA can be selectively packaged into sEVs under SAH, and this could help develop potential targets for the prevention, diagnosis, and treatment of CVS after this condition.
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spelling pubmed-74392192020-09-03 miRNA Profiling of Circulating Small Extracellular Vesicles From Subarachnoid Hemorrhage Rats Using Next-Generation Sequencing Lan, Shihai Zhou, Lin Wang, Yimei Fang, Linchun Yang, Le Zheng, Suyue Zhou, XinHui Tang, Bin Duan, Jian Wu, Xiao Yang, Chengxing Hong, Tao Front Cell Neurosci Neuroscience BACKGROUND: Extracellular vesicles (EVs) are produced during abnormal and normal physiological conditions. Understanding the expression profile of microRNA (miRNA) in plasma-derived small extracellular vesicles (sEVs) and their roles in subarachnoid hemorrhage (SAH) that cause cerebral vasospasm (CVS) is imperative. METHODS: Sprague Dawley rats (250–300 g) were allocated to sham or SAH groups established using endovascular perforation method. miRNA expression profiles of plasma sEVs in both groups (each n = 4) were evaluated using next-generation sequencing (NGS). RESULTS: There were 142 microRNAs (miRNAs) significantly expressed differently between the two groups, of which 73 were up-regulated while 69 were down-regulated in SAH sEVs compared with those of sham (p < 0.05; fold change ≥ 2). The Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway and Gene Ontology (GO) analyses of differently expressed (DE) miRNAs revealed signaling pathways and target genes (TGs) in the SAH group. rno-miR-185-5p, rno-miR-103-3p, rno-miR-15b-3p, rno-miR-93-5p, and rno-miR-98-5p were the top five most up-regulated sEVs miRNAs. CONCLUSION: Our results suggest that miRNA can be selectively packaged into sEVs under SAH, and this could help develop potential targets for the prevention, diagnosis, and treatment of CVS after this condition. Frontiers Media S.A. 2020-08-13 /pmc/articles/PMC7439219/ /pubmed/32903819 http://dx.doi.org/10.3389/fncel.2020.00242 Text en Copyright © 2020 Lan, Zhou, Wang, Fang, Yang, Zheng, Zhou, Tang, Duan, Wu, Yang and Hong. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Lan, Shihai
Zhou, Lin
Wang, Yimei
Fang, Linchun
Yang, Le
Zheng, Suyue
Zhou, XinHui
Tang, Bin
Duan, Jian
Wu, Xiao
Yang, Chengxing
Hong, Tao
miRNA Profiling of Circulating Small Extracellular Vesicles From Subarachnoid Hemorrhage Rats Using Next-Generation Sequencing
title miRNA Profiling of Circulating Small Extracellular Vesicles From Subarachnoid Hemorrhage Rats Using Next-Generation Sequencing
title_full miRNA Profiling of Circulating Small Extracellular Vesicles From Subarachnoid Hemorrhage Rats Using Next-Generation Sequencing
title_fullStr miRNA Profiling of Circulating Small Extracellular Vesicles From Subarachnoid Hemorrhage Rats Using Next-Generation Sequencing
title_full_unstemmed miRNA Profiling of Circulating Small Extracellular Vesicles From Subarachnoid Hemorrhage Rats Using Next-Generation Sequencing
title_short miRNA Profiling of Circulating Small Extracellular Vesicles From Subarachnoid Hemorrhage Rats Using Next-Generation Sequencing
title_sort mirna profiling of circulating small extracellular vesicles from subarachnoid hemorrhage rats using next-generation sequencing
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439219/
https://www.ncbi.nlm.nih.gov/pubmed/32903819
http://dx.doi.org/10.3389/fncel.2020.00242
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