Upregulation of miR-181a-5p and miR-125b-2-3p in the Maternal Circulation of Fetuses with Rh-Negative Hemolytic Disease of the Fetus and Newborn Could Be Related to Dysfunction of Placental Function.

Autor: Xie XH; Department of Obstetrics and Gynecology, The First People's Hospital of Neijiang City, Neijiang, Sichuan 641000, China., Jiang M; Department of Obstetrics and Gynecology, The First People's Hospital of Neijiang City, Neijiang, Sichuan 641000, China., Xiong ZA; Chongqing Medical University, Chongqing 400016, China.; Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing 400010, China., Huang XQ; Department of Obstetrics and Gynecology, The First People's Hospital of Neijiang City, Neijiang, Sichuan 641000, China.
Jazyk: angličtina
Zdroj: Disease markers [Dis Markers] 2022 Sep 21; Vol. 2022, pp. 2594091. Date of Electronic Publication: 2022 Sep 21 (Print Publication: 2022).
DOI: 10.1155/2022/2594091
Abstrakt: The transplacental transfer of maternal antibodies to the fetus is a critical mechanism for infant protection and perinatal disease. Hemolytic disease of the fetus and newborn (HDFN) is a representative fetal disease caused by transplacental transfer of maternal IgG antibodies. However, it is unclear whether placental-related miRNAs are expressed in Rh-HDFN. Through the investigation of the miR-181a-5p and miR-125b-2-3p levels in maternal plasma using qPCR, we found that both miR-181a-5p and miR-125b-2-3p were highly expressed in maternal plasma of newborns with Rh-HDFN compared with healthy controls, indicating the potential roles of these two miRNAs in Rh-HDFN. To demonstrate whether dysregulation of miR-125b-2-3p and miR-181a-5p contributes to Rh-HDFN development, we analyze the placental miRNA-/mRNA sequencing data (GSE73714) using weighted gene coexpression network analysis (WGCNA), miRNA target predictive databases, and DAVID (Database for Annotation, Visualization, and Integrated Discovery). The results showed that miR-125b-2-3p and miR-181a-5p could regulate several biological processes including cytoplasmic microtubule organization and angiogenesis. Moreover, core promoter sequence-specific DNA binding and protein binding were highly enriched molecular functions, indicating the potential roles of transcriptional regulation. Further pathway enrichment showed that miR-181a-5p and miR-125b-2-3p could regulate several biological pathways that were closely related to placental function, including the FoxO signaling pathway, focal adhesion, mTOR signaling pathway, and central carbon metabolism in cancer. In conclusion, the present results first revealed miRNA expression in the maternal circulation of newborns with Rh-HDFN, which could be caused by dysfunction of the placenta.
Competing Interests: All authors declare that there are no conflicts of interest.
(Copyright © 2022 Xiao-Hui Xie et al.)
Databáze: MEDLINE
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