Placental exosomes isolated from urine of patients with gestational diabetes exhibit a differential profile expression of microRNAs across gestation
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Placenta-derived exosomes play an important role in cellular communication both in the mother and the fetus. Their concentration and composition are altered in several pregnancy disorders, such as gestational diabetes mellitus (GDM). The isolation and characterization of placental exosomes from serum, plasma and tissues from patients with GDM have been previously described; however, to the best of our knowledge, to date, there is no study available on placental exosomes isolated from urine of patients with GDM. In the present study, placental exosomes were purified from urine the 1st, 2nd and 3rd trimester of gestation. Placental exosomes were characterized by transmission electron microscopy in cryogenic mode and by western blot analysis, confirming the presence of exosomal vesicles. The expression profile of five microRNAs (miR-516-5p, miR-517-3p, miR-518-5p, miR-222-3p and miR-16-5p) was determined by RT-qPCR. In healthy pregnant women, the expression of the miRNAs increased across gestation, apart from miR-516-5p, which was not expressed at the 2nd trimester. All the miRNAs examined were downregulated in patients with GDM at the 3rd trimester of gestation. The downregulated miRNAs affected several metabolic pathways closely associated with the pathophysiology of GDM. This provides further evidence of the regulatory role of miRNAs in the GDM. This also suggests that the of urinary exosomes may be an excellent source of biomarkers and therapeutic targets. © 2020 Spandidos Publications. All rights reserved.
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Biomarkers; Gestational diabetes; MicroRNAs; Placental exosomes biological marker; microRNA; microRNA 16 5p; microRNA 222 3p; microRNA 516 5p; microRNA 517 3p; microRNA 518 5p; unclassified drug; adult; Article; clinical article; controlled study; down regulation; exosome; female; first trimester pregnancy; gene expression profiling; gene function; gene targeting; gestation period; human; human cell; pathogenesis; pregnancy diabetes mellitus; priority journal; second trimester pregnancy; signal transduction; third trimester pregnancy; transmission electron microscopy; urinalysis
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