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Diagnostic Potential of Plasma Extracellular Vesicle miR-483-3p and Let-7d-3p for Sepsis

Background: microRNAs (miRNAs) from circulating extracellular vesicles (EVs) have been reported as disease biomarkers. This study aimed to identify the diagnostic value of plasma EV-miRNAs in sepsis. Methods: EVs were separated from the plasma of sepsis patients at admission and healthy controls. Th...

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Autores principales: Qiu, Guanguan, Fan, Jiajie, Zheng, Guoping, He, Jiangping, Lin, Fangping, Ge, Menghua, Huang, Lanfang, Wang, Jiangmei, Xia, Jie, Huang, Ruoqiong, Shu, Qiang, Xu, Jianguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847446/
https://www.ncbi.nlm.nih.gov/pubmed/35187084
http://dx.doi.org/10.3389/fmolb.2022.814240
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author Qiu, Guanguan
Fan, Jiajie
Zheng, Guoping
He, Jiangping
Lin, Fangping
Ge, Menghua
Huang, Lanfang
Wang, Jiangmei
Xia, Jie
Huang, Ruoqiong
Shu, Qiang
Xu, Jianguo
author_facet Qiu, Guanguan
Fan, Jiajie
Zheng, Guoping
He, Jiangping
Lin, Fangping
Ge, Menghua
Huang, Lanfang
Wang, Jiangmei
Xia, Jie
Huang, Ruoqiong
Shu, Qiang
Xu, Jianguo
author_sort Qiu, Guanguan
collection PubMed
description Background: microRNAs (miRNAs) from circulating extracellular vesicles (EVs) have been reported as disease biomarkers. This study aimed to identify the diagnostic value of plasma EV-miRNAs in sepsis. Methods: EVs were separated from the plasma of sepsis patients at admission and healthy controls. The expression of EV-miRNAs was evaluated by microarray and qRT-PCR. Results: A preliminary miRNA microarray of plasma EVs from a discovery cohort of 3 sepsis patients at admission and three healthy controls identified 11 miRNAs with over 2-fold upregulation in sepsis group. Based on this finding, EV samples from a validation cohort of 37 sepsis patients at admission and 25 healthy controls were evaluated for the expression of the 6 miRNAs relating injury and inflammation via qRT-PCR. Elevated expression of miR-483-3p and let-7d-3p was validated in sepsis patients and corroborated in a mouse model of sepsis. miR-483-3p and let-7d-3p levels positively correlated with the disease severity. Additionally, a combination of miR-483-3p and let-7d-3p had diagnostic value for sepsis. Furthermore, bioinformatic analysis and experimental validation showed that miR-483-3p and let-7d-3p target pathways regulating immune response and endothelial function. Conclusion: The present study reveals the potential role of plasma EV-miRNAs in the pathogenesis of sepsis and the utility of combining miR-483-3p and let-7d-3p as biomarkers for early sepsis diagnosis.
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spelling pubmed-88474462022-02-17 Diagnostic Potential of Plasma Extracellular Vesicle miR-483-3p and Let-7d-3p for Sepsis Qiu, Guanguan Fan, Jiajie Zheng, Guoping He, Jiangping Lin, Fangping Ge, Menghua Huang, Lanfang Wang, Jiangmei Xia, Jie Huang, Ruoqiong Shu, Qiang Xu, Jianguo Front Mol Biosci Molecular Biosciences Background: microRNAs (miRNAs) from circulating extracellular vesicles (EVs) have been reported as disease biomarkers. This study aimed to identify the diagnostic value of plasma EV-miRNAs in sepsis. Methods: EVs were separated from the plasma of sepsis patients at admission and healthy controls. The expression of EV-miRNAs was evaluated by microarray and qRT-PCR. Results: A preliminary miRNA microarray of plasma EVs from a discovery cohort of 3 sepsis patients at admission and three healthy controls identified 11 miRNAs with over 2-fold upregulation in sepsis group. Based on this finding, EV samples from a validation cohort of 37 sepsis patients at admission and 25 healthy controls were evaluated for the expression of the 6 miRNAs relating injury and inflammation via qRT-PCR. Elevated expression of miR-483-3p and let-7d-3p was validated in sepsis patients and corroborated in a mouse model of sepsis. miR-483-3p and let-7d-3p levels positively correlated with the disease severity. Additionally, a combination of miR-483-3p and let-7d-3p had diagnostic value for sepsis. Furthermore, bioinformatic analysis and experimental validation showed that miR-483-3p and let-7d-3p target pathways regulating immune response and endothelial function. Conclusion: The present study reveals the potential role of plasma EV-miRNAs in the pathogenesis of sepsis and the utility of combining miR-483-3p and let-7d-3p as biomarkers for early sepsis diagnosis. Frontiers Media S.A. 2022-02-02 /pmc/articles/PMC8847446/ /pubmed/35187084 http://dx.doi.org/10.3389/fmolb.2022.814240 Text en Copyright © 2022 Qiu, Fan, Zheng, He, Lin, Ge, Huang, Wang, Xia, Huang, Shu and Xu. https://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 Molecular Biosciences
Qiu, Guanguan
Fan, Jiajie
Zheng, Guoping
He, Jiangping
Lin, Fangping
Ge, Menghua
Huang, Lanfang
Wang, Jiangmei
Xia, Jie
Huang, Ruoqiong
Shu, Qiang
Xu, Jianguo
Diagnostic Potential of Plasma Extracellular Vesicle miR-483-3p and Let-7d-3p for Sepsis
title Diagnostic Potential of Plasma Extracellular Vesicle miR-483-3p and Let-7d-3p for Sepsis
title_full Diagnostic Potential of Plasma Extracellular Vesicle miR-483-3p and Let-7d-3p for Sepsis
title_fullStr Diagnostic Potential of Plasma Extracellular Vesicle miR-483-3p and Let-7d-3p for Sepsis
title_full_unstemmed Diagnostic Potential of Plasma Extracellular Vesicle miR-483-3p and Let-7d-3p for Sepsis
title_short Diagnostic Potential of Plasma Extracellular Vesicle miR-483-3p and Let-7d-3p for Sepsis
title_sort diagnostic potential of plasma extracellular vesicle mir-483-3p and let-7d-3p for sepsis
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847446/
https://www.ncbi.nlm.nih.gov/pubmed/35187084
http://dx.doi.org/10.3389/fmolb.2022.814240
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