4.5 Article

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

Journal

ENDOCRINOLOGY
Volume 160, Issue 2, Pages 249-275

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1210/en.2018-00836

Keywords

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Funding

  1. Bill and Melinda Gates Foundation
  2. Department of Biotechnology (DBT), Government of India
  3. Lions Medical Research Foundation
  4. National Health and Medical Research Council Grant [1114013]
  5. Fondo Nacional de Desarrollo Cientifico y Tecnologico Grant [1170809]
  6. National Health and Medical Research Council of Australia [1114013] Funding Source: NHMRC

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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-beta 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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