| First Author | Zeng YT | Year | 2023 |
| Journal | iScience | Volume | 26 |
| Issue | 10 | Pages | 107902 |
| PubMed ID | 37766993 | Mgi Jnum | J:342493 |
| Mgi Id | MGI:7538594 | Doi | 10.1016/j.isci.2023.107902 |
| Citation | Zeng YT, et al. (2023) GDF15 deficiency hinders human trophoblast invasion to mediate pregnancy loss through downregulating Smad1/5 phosphorylation. iScience 26(10):107902 |
| abstractText | Growth differentiation factor 15 (GDF15) belongs to the Transforming growth factor beta(TGF-beta) superfamily. The decrease of GDF15 in the serum of pregnant women was associated with miscarriage. Both IHC and ELISA assays showed that GDF15 in trophoblast tissue and serum of pregnant women who miscarried was significantly lower than in those who had a live birth. GDF15 deficiency was associated with embryo resorption in GDF15 knockout mice through CRIPSR editing. In addition, the migration and invasion ability of HTR-8/SVneo and JEG-3 cells were promoted by GDF15. Mechanistically, GDF15 increased Smad1/5 phosphorylation, resulting in upregulating SNAI1/2, VIMENTIN and downregulating E-CADHERIN. A dual-luciferase reporter assay confirmed that Smad-binding elements (SBE) and/or GC-rich motifs were activated and target genes such as SNAI1/2, SERPINE1, and TIMP3 were transcriptionally regulated by GDF15/Smad5 signaling. Therefore, our data revealed a crucial role of GDF15 on invasion of trophoblast by upregulating the activity of TGF-beta/Smad1/5 pathway. |
