MicroRNA Regulation of Mitogenic Signaling Networks in the Human Placenta

• Published in: The Journal of biological chemistry Vol. 289; no. 44; pp. 30404 - 30416
• Main Authors: Farrokhnia, Farkhondeh, Aplin, John D., Westwood, Melissa, Forbes, Karen
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 31.10.2014; American Society for Biochemistry and Molecular Biology
• Subjects: Cell Line; Cell Proliferation; Developmental Biology; Female; Gene Regulatory Networks; Humans; MicroRNAs - physiology; Mitosis - genetics; Placenta - cytology; Placenta - metabolism; Pregnancy; Pregnancy Trimester, First; RNA Interference; Signal Transduction; Somatomedins - physiology; Transcriptome; Trophoblasts - physiology; Gene Regulation; Reproduction; Placenta; MicroRNA (miRNA); Trophoblast; Proliferation; Insulin-like Growth Factor (IGF); Developmental Factor
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M114.587295

Placental cell growth depends on an adaptable combination of an endogenous developmental program and the exogenous influence of maternal growth factors, both of which may be influenced by microRNA (miR)-dependent effects on gene expression. We have previously shown that global miR suppression in placenta accelerates proliferation and enhances levels of growth factor signaling mediators in cytotrophoblast. This study aimed to identify miRs involved in regulating placental growth. An initial array revealed 58 miR species whose expression differs between first trimester, when cytotrophoblast proliferation is rapid, and term, by which time proliferation has slowed. In silico analysis defined potential growth-regulatory miRs; among these, hsa-miR-145, hsa-miR-377, and hsa-let-7a were predicted to target known placental growth genes and were higher at term than in the first trimester, so they were selected for further analysis. Overexpression of miR-377 and let-7a, but not miR-145, in first trimester placental explants significantly reduced basal cytotrophoblast proliferation and expression of ERK and MYC. PCR arrays, in silico analysis, Western blotting, and 3′-UTR luciferase reporter assays revealed targets of miR-145 within the insulin-like growth factor axis. Analysis of proliferation in placental explants overexpressing miR-145 demonstrated its role as a mediator of insulin-like growth factor-induced trophoblast proliferation. These findings identify miR-377 and let-7a in regulation of endogenous cell growth and miR-145 in the placental response to maternal stimulation and will aid the development of therapeutic strategies for problem pregnancies.