Cellular signalling · 2025
WTAP targets SOX2 to inhibit trophoblast ferroptosis in the pathogenesis of preeclampsia via m6A-dependent ferroptosis regulation.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Geng Hao, Zhou Limei, Zhang Pei, Li Xing, Guo Ying, Cui Hongyan, Chen Xu
Аннотация
BACKGROUND: Preeclampsia (PE) is associated with trophoblast damage, which may be caused by aberrant ferroptosis, an important process in placental development and function. The key component of N6-methyladenosine (m6A)-wilms tumor 1 associated protein (WTAP) has been reported to be involved in the migration and invasion of trophoblasts in the pathogenesis of PE. However, the connection between WTAP and ferroptosis in PE remained poorly understood. Accordingly, in order to explore potential treatments for PE, and understand how WTAP influences the trophoblasts' ferroptosis in PE, researchers conducted in vitro and in vivo experiments.
METHODS: Relevant molecular biology assays were conducted to investigate the effect of WTAP.
RESULTS: Here, we report that both m6A and WTAP levels were downregulated in placental tissue samples of 20 PE participants and the hypoxia model of trophoblast cell line HTR-8/SVneo, and down-regulation of WTAP promotes PE progression through m6A-dependent ferroptosis regulation. Stem cell transcriptional factor (SOX2) can specifically bind to the promoters of ferroptosis-related genes GPX4, SLC7A11, and FTH1 to regulate their expression in HTR-8/SVneo cells. In terms of molecular mechanisms, WTAP in trophoblast targeted the SOX2 gene. Through binding to its 3'-UTR m6A site, WTAP increased the stability of SOX2 mRNA. Moreover, animal studies demonstrated that WTAP could suppress ferroptosis and alleviate the symptoms of preeclampsia in the rat model of preeclampsia via SOX2.
CONCLUSION: WTAP mediates the m6A modification of SOX2 to regulate trophoblast ferroptosis in vitro and in vivo. Our findings point to a novel approach to treating PE and provide the groundwork for future research into this disease's RNA epigenetic regulation mechanisms.
METHODS: Relevant molecular biology assays were conducted to investigate the effect of WTAP.
RESULTS: Here, we report that both m6A and WTAP levels were downregulated in placental tissue samples of 20 PE participants and the hypoxia model of trophoblast cell line HTR-8/SVneo, and down-regulation of WTAP promotes PE progression through m6A-dependent ferroptosis regulation. Stem cell transcriptional factor (SOX2) can specifically bind to the promoters of ferroptosis-related genes GPX4, SLC7A11, and FTH1 to regulate their expression in HTR-8/SVneo cells. In terms of molecular mechanisms, WTAP in trophoblast targeted the SOX2 gene. Through binding to its 3'-UTR m6A site, WTAP increased the stability of SOX2 mRNA. Moreover, animal studies demonstrated that WTAP could suppress ferroptosis and alleviate the symptoms of preeclampsia in the rat model of preeclampsia via SOX2.
CONCLUSION: WTAP mediates the m6A modification of SOX2 to regulate trophoblast ferroptosis in vitro and in vivo. Our findings point to a novel approach to treating PE and provide the groundwork for future research into this disease's RNA epigenetic regulation mechanisms.