miR-218-5p Induces Interleukin-1β and Endovascular Trophoblast Differentiation by Targeting the Transforming Growth Factor β-SMAD2 Pathway

The acquisition of an endovascular trophoblast (enEVT) phenotype is essential for normal placental development and healthy pregnancy. MicroRNAs (miRNAs) are small noncoding RNAs that play critical roles in regulating gene expression. We have recently reported that miR-218-5p promotes enEVT differentiation and spiral artery remodeling in part by targeting transforming growth factor beta 2 (TGF beta 2). We also identified IL1B, which encodes interleukin 1 beta (IL1 beta), as one of the most highly upregulated genes by miR-218-5p. In this study, we investigated how miR-218-5p regulates IL1B expression and IL1 beta secretion and the potential role of IL1 beta in enEVT differentiation. Using two cell lines derived from extravillous trophoblasts (EVTs), HTR-8/SVneo and Swan 71, we found that stable overexpression of miR-218-5p precursor, mir-218-1, or transient transfection of miR-218-5p mimic, significantly increased IL1B mRNA and IL1 beta protein levels in cells and conditioned media. We also showed that miR-218-5p directly interacted with SMAD2 3'UTR and reduced SMAD2 at mRNA and protein levels. Knockdown of SMAD2 induced IL1B expression and attenuated the inhibitory effect of TGF beta 2 on IL1B expression. On the other hand, overexpression of SMAD2 reduced IL1 beta levels and blocked the stimulatory effects of miR-218-5p on IL1B expression, trophoblast migration and endothelial-like network formation. In addition, treatment of trophoblasts with IL1 beta induced the formation of endothelial-like networks and the expression of enEVT markers in a dose-dependent manner. These results suggest that miR-218-5p inhibits the TGF beta/SMAD2 pathway to induce IL1 beta and enEVT differentiation. Finally, low doses of IL1 beta also inhibited the expression of miR-218-5p, suggesting the existence of a negative feedback regulatory loop. Taken together, our findings suggest a novel interactive miR-218-5p/TGF beta/SMAD2/IL1 beta signaling nexus that regulates enEVT differentiation.

Automated summary

miR-218-5p inhibits the TGF-β/SMAD2 pathway to induce IL1β expression and promote enEVT differentiation. IL1β, in turn, inhibits the expression of miR-218-5p, forming a negative feedback regulatory loop.