Circulating Extracellular Vesicles microRNAs Are Altered in Women Undergoing Preterm Birth

Author:

Ramos Bruna Ribeiro Andrade12,Tronco Júlia Abbade1ORCID,Carvalho Márcio3,Felix Tainara Francini4,Reis Patrícia Pintor5ORCID,Silveira Juliano Coelho6ORCID,Silva Márcia Guimarães1

Affiliation:

1. Department of Pathology, Botucatu Medical School, São Paulo State University (UNESP), Botucatu 17213-700, SP, Brazil

2. Faculty of Medicine—Jaú Campus, University of Western São Paulo (UNOESTE), Jaú 17213-700, SP, Brazil

3. Faculty of Veterinary Medicine and Animal Science, São Paulo State University (UNESP), Botucatu 17213-700, SP, Brazil

4. Experimental Research Unity (UNIPEX), Botucatu Medical School, São Paulo State University (UNESP), Botucatu 17213-700, SP, Brazil

5. Department of Surgery and Orthopedics, Botucatu Medical School, São Paulo State University (UNESP), Botucatu 17213-700, SP, Brazil

6. Department of Veterinary Medicine, Faculty of Animal Science and Food Engineering, São Paulo University (USP), Pirassununga 13635-900, SP, Brazil

Abstract

Preterm labor (PTL) and preterm premature rupture of membranes (PPROM) lead to high perinatal morbidity/mortality rates worldwide. Small extracellular vesicles (sEV) act in cell communication and contain microRNAs that may contribute to the pathogenesis of these complications. We aimed to compare the expression, in sEV from peripheral blood, of miRNAs between term and preterm pregnancies. This cross-sectional study included women who underwent PTL, PPROM, and term pregnancies, examined at the Botucatu Medical School Hospital, SP, Brazil. sEV were isolated from plasma. Western blot used to detect exosomal protein CD63 and nanoparticle tracking analysis were performed. The expression of 800 miRNAs was assessed by the nCounter Humanv3 miRNA Assay (NanoString). The miRNA expression and relative risk were determined. Samples from 31 women—15 preterm and 16 term—were included. miR-612 expression was increased in the preterm groups. miR-612 has been shown to increase apoptosis in tumor cells and to regulate the nuclear factor κB inflammatory pathway, processes involved in PTL/PPROM pathogenesis. miR-1253, miR-1283, miR378e, and miR-579-3p, all associated with cellular senescence, were downregulated in PPROM compared with term pregnancies. We conclude that miRNAs from circulating sEV are differentially expressed between term and preterm pregnancies and modulate genes in pathways that are relevant to PTL/PPROM pathogenesis.

Funder

São Paulo Research Foundation

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference61 articles.

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4. Brain damage in preterm infants: Etiological pathways;Arpino;Ann. Dell’istituto Super. Sanitã,2005

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