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Circulating Exosomal miRNA Profile During Term and Preterm Birth Pregnancies: A Longitudinal Study

Despite decades of research in the field of human reproduction, the mechanisms responsible for human parturition still remain elusive. The objective of this study was to describe the changes in the exosomal miRNA concentrations circulating in the maternal plasma between mothers delivering term and p...

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Autores principales: Menon, Ramkumar, Debnath, Chirantan, Lai, Andrew, Guanzon, Dominic, Bhatnagar, Shinjini, Kshetrapal, Pallavi K, Sheller-Miller, Samantha, Salomon, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394761/
https://www.ncbi.nlm.nih.gov/pubmed/30358826
http://dx.doi.org/10.1210/en.2018-00836
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author Menon, Ramkumar
Debnath, Chirantan
Lai, Andrew
Guanzon, Dominic
Bhatnagar, Shinjini
Kshetrapal, Pallavi K
Sheller-Miller, Samantha
Salomon, Carlos
author_facet Menon, Ramkumar
Debnath, Chirantan
Lai, Andrew
Guanzon, Dominic
Bhatnagar, Shinjini
Kshetrapal, Pallavi K
Sheller-Miller, Samantha
Salomon, Carlos
author_sort Menon, Ramkumar
collection PubMed
description Despite decades of research in the field of human reproduction, the mechanisms responsible for human parturition still remain elusive. The objective of this study was to describe the changes in the exosomal miRNA concentrations circulating in the maternal plasma between mothers delivering term and preterm neonates, across gestation using a longitudinal study design. This descriptive study identifies the miRNA content in exosomes present in maternal plasma of term and preterm birth (PTB) (n = 20 and n = 10 per each gestational period, respectively) across gestation (i.e., first, second, and third trimesters and at the time of delivery). Changes in exosomal miRNA signature in maternal plasma during term and preterm gestation were determined using the NextSeq 500 high-output 75 cycles sequencing platform. A total of 167 and 153 miRNAs were found to significantly change (P < 0.05) as a function of the gestational age across term and PTB pregnancies, respectively. Interestingly, a comparison analysis between the exosomal miRNA profile between term and PTB reveals a total of 173 miRNAs that significantly change (P < 0.05) across gestation. Specific trends of changes (i.e., increase, decrease, and both) as a function of the gestational age were also identified. The bioinformatics analyses establish that the differences in the miRNA profile are targeting signaling pathways associated with TGF-β signaling, p53, and glucocorticoid receptor signaling, respectively. These data suggest that the miRNA content of circulating exosomes in maternal blood might represent a biomolecular “fingerprint” of the progression of pregnancy.
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spelling pubmed-63947612019-03-05 Circulating Exosomal miRNA Profile During Term and Preterm Birth Pregnancies: A Longitudinal Study Menon, Ramkumar Debnath, Chirantan Lai, Andrew Guanzon, Dominic Bhatnagar, Shinjini Kshetrapal, Pallavi K Sheller-Miller, Samantha Salomon, Carlos Endocrinology Research Articles Despite decades of research in the field of human reproduction, the mechanisms responsible for human parturition still remain elusive. The objective of this study was to describe the changes in the exosomal miRNA concentrations circulating in the maternal plasma between mothers delivering term and preterm neonates, across gestation using a longitudinal study design. This descriptive study identifies the miRNA content in exosomes present in maternal plasma of term and preterm birth (PTB) (n = 20 and n = 10 per each gestational period, respectively) across gestation (i.e., first, second, and third trimesters and at the time of delivery). Changes in exosomal miRNA signature in maternal plasma during term and preterm gestation were determined using the NextSeq 500 high-output 75 cycles sequencing platform. A total of 167 and 153 miRNAs were found to significantly change (P < 0.05) as a function of the gestational age across term and PTB pregnancies, respectively. Interestingly, a comparison analysis between the exosomal miRNA profile between term and PTB reveals a total of 173 miRNAs that significantly change (P < 0.05) across gestation. Specific trends of changes (i.e., increase, decrease, and both) as a function of the gestational age were also identified. The bioinformatics analyses establish that the differences in the miRNA profile are targeting signaling pathways associated with TGF-β signaling, p53, and glucocorticoid receptor signaling, respectively. These data suggest that the miRNA content of circulating exosomes in maternal blood might represent a biomolecular “fingerprint” of the progression of pregnancy. Endocrine Society 2018-10-24 /pmc/articles/PMC6394761/ /pubmed/30358826 http://dx.doi.org/10.1210/en.2018-00836 Text en Copyright © 2019 Endocrine Society https://creativecommons.org/licenses/by/4.0/ This article has been published under the terms of the Creative Commons Attribution License (CC BY; https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Menon, Ramkumar
Debnath, Chirantan
Lai, Andrew
Guanzon, Dominic
Bhatnagar, Shinjini
Kshetrapal, Pallavi K
Sheller-Miller, Samantha
Salomon, Carlos
Circulating Exosomal miRNA Profile During Term and Preterm Birth Pregnancies: A Longitudinal Study
title Circulating Exosomal miRNA Profile During Term and Preterm Birth Pregnancies: A Longitudinal Study
title_full Circulating Exosomal miRNA Profile During Term and Preterm Birth Pregnancies: A Longitudinal Study
title_fullStr Circulating Exosomal miRNA Profile During Term and Preterm Birth Pregnancies: A Longitudinal Study
title_full_unstemmed Circulating Exosomal miRNA Profile During Term and Preterm Birth Pregnancies: A Longitudinal Study
title_short Circulating Exosomal miRNA Profile During Term and Preterm Birth Pregnancies: A Longitudinal Study
title_sort circulating exosomal mirna profile during term and preterm birth pregnancies: a longitudinal study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394761/
https://www.ncbi.nlm.nih.gov/pubmed/30358826
http://dx.doi.org/10.1210/en.2018-00836
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