MicroRNA-548 regulates high mobility group box 1 expression in patients with preterm birth and chorioamnionitis

• Published in: Scientific reports 2019-12, Vol.9 (1), p.19746-12, Article 19746
• Main Authors: Son, Ga-Hyun, Kim, Youngmi, Lee, Jae Jun, Lee, Keun-Young, Ham, Heejin, Song, Ji-Eun, Park, Sung Taek, Kim, Young-Han
• Format: Article
• Language: English
• Subjects: 13; 13/1; 13/109; 13/21; 631/337/384/331; 692/308/575; Adult; Amnion; Amnion - metabolism; Amnion - pathology; Amniotic fluid; Bioinformatics; Birth; Chorioamnionitis; Chorioamnionitis - metabolism; Chorioamnionitis - pathology; Cytokines; Epithelial cells; Epithelial Cells - metabolism; Epithelial Cells - pathology; Female; Gene Expression Regulation; HMGB1 protein; HMGB1 Protein - biosynthesis; Humanities and Social Sciences; Humans; Infant, Newborn; Inflammation; Lipopolysaccharides; MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; miRNA; Mobility; multidisciplinary; Pathogenesis; Pregnancy; Premature birth; Premature Birth - metabolism; Premature Birth - pathology; Science; Science (multidisciplinary)
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-019-56327-9

High mobility group box 1 (HMGB1) is a prototypic alarmin and plays an important role in the pathogenesis of inflammatory process in spontaneous preterm birth. This study was conducted to compare the levels of HMGB1 in amniotic fluid and amnion membranes in women with chorioamnionitis/intra-amniotic inflammation to the levels in healthy controls. We also aimed to elucidate the involvement of microRNA-548 (miR-548) in regulating HMGB1 expression and its function in human amniotic epithelial cells (hAECs). A bioinformatics analysis predicted the binding of HMGB1 by the miR-548 cluster. A repressed and forced expression assay in hAECs was performed to investigate the causal relationship between the miR-548 cluster and HMGB1. The levels of HMGB1 in amniotic fluid and amnion membranes were significantly higher in patients with intra-amniotic inflammation/chorioamnionitis than in those without inflammation. The miR-548 was significantly under-expressed in amnion membranes from patients with chorioamnionitis than in normal term controls. Repressed expression of miR-548 up-regulated HMGB1 expression in hAECs and increased its release from hAECs. Moreover, forced expression of miR-548 suppressed HMGB1 and inflammatory cytokines in hAECs, which increased when treated with lipopolysaccharide. These results suggest miR-548 can alter the inflammatory responses in hAECs, and might be involved in the pathogenesis of preterm birth by regulating HMGB1.