2022
DOI: 10.1007/s43032-022-00939-6
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Human Trophoblast Cell-Derived Extracellular Vesicles Facilitate Preeclampsia by Transmitting miR-1273d, miR-4492, and miR-4417 to Target HLA-G

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Cited by 11 publications
(7 citation statements)
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“…MiR-1273d was found to be involved in hypoxia, immune, and inflammatory pathways. 33 MiR-1303 and miR-3064-5p regulate the permeability of the blood–brain barrier, 34 , 35 increasing the risk of viral infection or damage to the brain by toxic substances, ultimately leading to pathological changes in the central nervous system. MiR-4428 is involved in the PI3K-PKB signaling pathway that promotes cell survival.…”
Section: Discussionmentioning
confidence: 99%
“…MiR-1273d was found to be involved in hypoxia, immune, and inflammatory pathways. 33 MiR-1303 and miR-3064-5p regulate the permeability of the blood–brain barrier, 34 , 35 increasing the risk of viral infection or damage to the brain by toxic substances, ultimately leading to pathological changes in the central nervous system. MiR-4428 is involved in the PI3K-PKB signaling pathway that promotes cell survival.…”
Section: Discussionmentioning
confidence: 99%
“…EVs derived from hypoxic trophoblast cells regulate chondroitin polymerizing factor by delivering miR-150–3p to inhibit endothelial cell proliferation, migration, and angiogenesis [ 53 ]. EVs secreted by trophoblast cells under hypoxic conditions transferred miR-1273d, miR-4492, and miR-4417 to coordinate immune- and inflammation-related pathways to promote PE development [ 54 ]. Exos-MSC may alleviate the apoptosis of PE and promote the angiogenesis of placental tissue [ 16 ].…”
Section: Discussionmentioning
confidence: 99%
“…Also, placental tissues from PE patients showed a significantly decreased Foxp3 and significantly increased expression of miR-210, indicating a possibly positive co-regulation among them [78]. In vitro assays showed that under hypoxic conditions, human trophoblast cell-derived extracellular vesicles release miR-1273d, miR-4492, and miR-4417 to target HLA-G, mediating immune-and inflammation-related pathways and, consequently, triggering the development of PE [79].…”
Section: Mirnas In the Immune Dysregulation Of Preeclampsiamentioning
confidence: 97%