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| Item Type: | Preprint |
|---|---|
| Title: | TGFb-induced SMAD1/5 activation drives transient epithelial-to-mesenchymal transition in trophoblasts |
| Creators Name: | Mähr, Sophia, Ingolfsdottir, Hallfridur, Alexdottir, Marta Sorokina, Hartmann, Sunhild, Nonn, Olivia, Gunnarsdottir, Johanna, Steingrimsdottir, Þóra, Jatzlau, Jerome, Knaus, Petra and Valdimarsdottir, Gudrun |
| Abstract: | Successful human placental development requires fetal trophoblasts to undergo epithelial-to-mesenchymal and mesenchymal-to-endothelial transitions, enabling invasion and remodeling of maternal spiral arteries for proper placental perfusion. These trans-differentiation processes are disrupted in preeclampsia, a major cause of maternal and fetal morbidity worldwide. Despite its clinical significance, the molecular mechanisms governing these differentiation trajectories at the fetal-maternal interface remain poorly defined. While Transforming Growth Factor-beta (TGFβ) has been implicated in trophoblast invasion, its role remains controversial. In this study, we report increased SMAD2/3 phosphorylation (pSMAD2/3), but reduced pSMAD1/5 and SNAIL levels in preeclamptic placentas. Mechanistically, we show that TGFβ1 induces transient SMAD1/5 phosphorylation via dual engagement of the TGFβ type I receptor ALK5 and the BMP type I receptor ALK2 in both HTR8/SVneo cells and human trophoblast stem cells. Moreover, single-nucleus transcriptomics of first-trimester placentas revealed co-expression of ACVR1, TGFBR1, SMAD1 and SMAD5 at the transition zone between cytotrophoblasts and extravillous trophoblasts. Our findings suggest that transient TGFβ-induced ALK5/ALK2-SMAD1/5 signaling is critical for EMT initiation, a prerequisite for proper placental differentiation. |
| Keywords: | Differentiation, Placenta, Preeclampsia, TGFbeta, SMAD1, 5, Trophoblasts |
| Source: | bioRxiv |
| Publisher: | Cold Spring Harbor Laboratory Press |
| Article Number: | 2025.07.21.665880 |
| Date: | 25 July 2025 |
| Official Publication: | https://doi.org/10.1101/2025.07.21.665880 |
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