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Profiling of exosomal microRNAs expression in umbilical cord blood from normal and preeclampsia patients

BACKGROUND: Epidemiological and experimental studies suggest that preeclampsia has a negative impact on maternity and offspring health. Previous studies report that dysregulation in utero-environment increases risk for elderly disease such as cardiovascular disease. However, the underlying mechanism...

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Autores principales: Pan, Hai-Tao, Shi, Xiao-Liang, Fang, Min, Sun, Xiang-Mei, Chen, Pan-Pan, Ding, Jin-Long, Xia, Gui-Yu, Yu, Bin, Zhang, Tao, Zhu, Hong-Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842963/
https://www.ncbi.nlm.nih.gov/pubmed/35152894
http://dx.doi.org/10.1186/s12884-022-04449-w
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author Pan, Hai-Tao
Shi, Xiao-Liang
Fang, Min
Sun, Xiang-Mei
Chen, Pan-Pan
Ding, Jin-Long
Xia, Gui-Yu
Yu, Bin
Zhang, Tao
Zhu, Hong-Dan
author_facet Pan, Hai-Tao
Shi, Xiao-Liang
Fang, Min
Sun, Xiang-Mei
Chen, Pan-Pan
Ding, Jin-Long
Xia, Gui-Yu
Yu, Bin
Zhang, Tao
Zhu, Hong-Dan
author_sort Pan, Hai-Tao
collection PubMed
description BACKGROUND: Epidemiological and experimental studies suggest that preeclampsia has a negative impact on maternity and offspring health. Previous studies report that dysregulation in utero-environment increases risk for elderly disease such as cardiovascular disease. However, the underlying mechanisms remain elusive. Specific microRNAs (miRNAs) are packaged in exosomes may regulate microvascular dysfunction in offspring of mothers with preeclampsia. The present study aimed to identify the differential expression profiles of microRNAs in the serum exosomes between patients with preeclampsia and normal pregnancies. METHODS: A comprehensive miRNA sequence-based approach was performed to compare exosomes carry miRNAs (Exo-miRNAs) expression levels in umbilical serum between normal and preeclampsia patients. Exosomes were isolated using the ExoQuick precipitation kit. Serum exosomes were then viewed under electron microscopy, and their characteristics determined by western blotting and nanoparticle-tracking analysis. Illumina platform was used to perform sequencing. Bioinformatics analysis was used to explore differentially expressed Exo-miRNAs in umbilical serum. RESULTS: Based on sequence similarity, 1733 known miRNAs were retrieved. Furthermore, 157 mature miRNAs in serum exosomes were significantly differential expressed between PE and those control groups (P<0.05, log(2)|FC| > 1). Out, of the 157 miRNAs, 96 were upregulated miRNAs whereas 61 miRNAs were downregulated. The 157 differentially expressed miRNAs targeted 51,424 differentially expressed genes. Functional analysis through KEGG pathway and Gene Ontology results uncovered that target genes of miRNAs with differential expression were significantly linked to several pathways and biological processes. CONCLUSION: The findings of this study showed differential expression of umbilical serum Exo-miRNAs in normal compared with PE patients, implying that these Exo-miRNAs may associate with microvascular dysfunction in offspring of mothers with preeclampsia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-022-04449-w.
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spelling pubmed-88429632022-02-16 Profiling of exosomal microRNAs expression in umbilical cord blood from normal and preeclampsia patients Pan, Hai-Tao Shi, Xiao-Liang Fang, Min Sun, Xiang-Mei Chen, Pan-Pan Ding, Jin-Long Xia, Gui-Yu Yu, Bin Zhang, Tao Zhu, Hong-Dan BMC Pregnancy Childbirth Research BACKGROUND: Epidemiological and experimental studies suggest that preeclampsia has a negative impact on maternity and offspring health. Previous studies report that dysregulation in utero-environment increases risk for elderly disease such as cardiovascular disease. However, the underlying mechanisms remain elusive. Specific microRNAs (miRNAs) are packaged in exosomes may regulate microvascular dysfunction in offspring of mothers with preeclampsia. The present study aimed to identify the differential expression profiles of microRNAs in the serum exosomes between patients with preeclampsia and normal pregnancies. METHODS: A comprehensive miRNA sequence-based approach was performed to compare exosomes carry miRNAs (Exo-miRNAs) expression levels in umbilical serum between normal and preeclampsia patients. Exosomes were isolated using the ExoQuick precipitation kit. Serum exosomes were then viewed under electron microscopy, and their characteristics determined by western blotting and nanoparticle-tracking analysis. Illumina platform was used to perform sequencing. Bioinformatics analysis was used to explore differentially expressed Exo-miRNAs in umbilical serum. RESULTS: Based on sequence similarity, 1733 known miRNAs were retrieved. Furthermore, 157 mature miRNAs in serum exosomes were significantly differential expressed between PE and those control groups (P<0.05, log(2)|FC| > 1). Out, of the 157 miRNAs, 96 were upregulated miRNAs whereas 61 miRNAs were downregulated. The 157 differentially expressed miRNAs targeted 51,424 differentially expressed genes. Functional analysis through KEGG pathway and Gene Ontology results uncovered that target genes of miRNAs with differential expression were significantly linked to several pathways and biological processes. CONCLUSION: The findings of this study showed differential expression of umbilical serum Exo-miRNAs in normal compared with PE patients, implying that these Exo-miRNAs may associate with microvascular dysfunction in offspring of mothers with preeclampsia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-022-04449-w. BioMed Central 2022-02-14 /pmc/articles/PMC8842963/ /pubmed/35152894 http://dx.doi.org/10.1186/s12884-022-04449-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Pan, Hai-Tao
Shi, Xiao-Liang
Fang, Min
Sun, Xiang-Mei
Chen, Pan-Pan
Ding, Jin-Long
Xia, Gui-Yu
Yu, Bin
Zhang, Tao
Zhu, Hong-Dan
Profiling of exosomal microRNAs expression in umbilical cord blood from normal and preeclampsia patients
title Profiling of exosomal microRNAs expression in umbilical cord blood from normal and preeclampsia patients
title_full Profiling of exosomal microRNAs expression in umbilical cord blood from normal and preeclampsia patients
title_fullStr Profiling of exosomal microRNAs expression in umbilical cord blood from normal and preeclampsia patients
title_full_unstemmed Profiling of exosomal microRNAs expression in umbilical cord blood from normal and preeclampsia patients
title_short Profiling of exosomal microRNAs expression in umbilical cord blood from normal and preeclampsia patients
title_sort profiling of exosomal micrornas expression in umbilical cord blood from normal and preeclampsia patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842963/
https://www.ncbi.nlm.nih.gov/pubmed/35152894
http://dx.doi.org/10.1186/s12884-022-04449-w
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