Stem cell research & therapy · 2025
Umbilical cord mesenchymal stem cells protect against obstetric deep venous thrombosis in rats by suppressing ferroptosis.
СтатьяНазвание и аннотация: Перевод в очереди
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Cheng Xi, Zhang Junrong, Wang Weina, Xia Dongqin, Liu Lehan, Xie Yuanyuan, Du Rong, Ni Juanjuan, Zhang Mu, Ji Jingjing, Zhang Hao, Sun Huihua, Sun Baolan, Zhang Yuquan
Аннотация
BACKGROUND: The objective of the current investigation is to explore the role of ferroptosis in mediating the protective effects associated with umbilical cord mesenchymal stem cells (UCMSCs) on obstetric deep venous thrombosis (DVT) in vivo and in vitro.
METHODS: A pregnant rat model of DVT was created through the application of a "stenosis" technique targeting the inferior vena cava (IVC). Furthermore, the protective effects of UCMSCs were evaluated on pregnant rats with DVT and impaired endothelial cells. Subsequently, transcriptome sequencing was utilized to pinpoint the genes that exhibited differential expression in the thrombosed IVC tissues of rats belonging to both the DVT) and DVT + UCMSC groups. Finally, the role of the candidate gene was demonstrated.
RESULTS: The administration of UCMSCs into pregnant rats diagnosed with DVT notably led to a greater degree of angiogenesis, alleviated coagulation, inflammation, and ferroptosis, and ameliorated the pregnancy outcomes. In vitro, erastin induced typical features related to ferroptosis. UCMSC-conditioned medium (UC-CM) effectively enhanced the capacity of dysfunctional endothelial cells to undergo proliferation, migration, invasion, and the formation of vessel-like structures, and normalized the levels of reactive oxygen species and malondialdehyde. The analysis of KEGG pathway enrichment revealed that the signaling pathway associated with ferroptosis in the thrombosed tissues of rats in the UCMSC group markedly suppressed. The levels of arachidonate-15-lipoxygenase (ALOX15), a marker related to ferroptosis, was significantly downregulated in both thrombosed tissues and endothelial cells sorted out from these tissues after UCMSC transplantation. Furthermore, the function of ALOX15 was verified in vitro and in vivo. In conclusion, this study suggested that UCMSCs mitigated the inflammation levels, facilitated recanalization, and improved pregnancy outcomes in cases of obstetric DVT by mitigating ferroptosis within endothelial cells.
METHODS: A pregnant rat model of DVT was created through the application of a "stenosis" technique targeting the inferior vena cava (IVC). Furthermore, the protective effects of UCMSCs were evaluated on pregnant rats with DVT and impaired endothelial cells. Subsequently, transcriptome sequencing was utilized to pinpoint the genes that exhibited differential expression in the thrombosed IVC tissues of rats belonging to both the DVT) and DVT + UCMSC groups. Finally, the role of the candidate gene was demonstrated.
RESULTS: The administration of UCMSCs into pregnant rats diagnosed with DVT notably led to a greater degree of angiogenesis, alleviated coagulation, inflammation, and ferroptosis, and ameliorated the pregnancy outcomes. In vitro, erastin induced typical features related to ferroptosis. UCMSC-conditioned medium (UC-CM) effectively enhanced the capacity of dysfunctional endothelial cells to undergo proliferation, migration, invasion, and the formation of vessel-like structures, and normalized the levels of reactive oxygen species and malondialdehyde. The analysis of KEGG pathway enrichment revealed that the signaling pathway associated with ferroptosis in the thrombosed tissues of rats in the UCMSC group markedly suppressed. The levels of arachidonate-15-lipoxygenase (ALOX15), a marker related to ferroptosis, was significantly downregulated in both thrombosed tissues and endothelial cells sorted out from these tissues after UCMSC transplantation. Furthermore, the function of ALOX15 was verified in vitro and in vivo. In conclusion, this study suggested that UCMSCs mitigated the inflammation levels, facilitated recanalization, and improved pregnancy outcomes in cases of obstetric DVT by mitigating ferroptosis within endothelial cells.