LOX-1 expression is reduced in placenta from pregnancies complicated by preeclampsia and in hypoxic cytotrophoblast
Pregnancy Hypertension, ISSN: 2210-7789, Vol: 25, Page: 255-261
2021
- 3Citations
- 14Captures
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Metrics Details
- Citations3
- Citation Indexes3
- Captures14
- Readers14
- 14
Article Description
The lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) is upregulated in the maternal vasculature in preeclampsia, and contributes to oxidative stress and endothelial dysfunction. However, its function in the placenta is unclear. This paper investigated LOX-1 expression in models of placental dysfunction and preeclampsia, and whether candidate therapeutics for preeclampsia could alter its expression. Placentas were collected from preterm pregnancies and cases of preterm preeclampsia and fetal growth restriction. Blood was collected from participants whose pregnancies were complicated by preterm fetal growth restriction and/or preeclampsia. Primary cytotrophoblast and placental explant tissue were cultured under hypoxic (1% O 2 ) or normoxic (8% O 2 ) conditions. Cytotrophoblast were exposed to 10% preeclamptic or control serum. Cytotrophoblast and preeclamptic explant tissue were treated with 100 µM esomeprazole, lansoprazole or rabeprazole. LOX-1 expression was assessed in all samples via qPCR. LOX-1 expression was reduced in placentas from cases of preterm preeclampsia, but not fetal growth restriction, compared to controls. LOX-1 expression was reduced in cytotrophoblast under hypoxia, but not in explant tissue. Treatment with preeclamptic serum in vitro did not alter cytotrophoblast LOX-1 expression. Circulating LOX-1 mRNA was unaltered in patients with fetal growth restriction, preeclampsia, and fetal hypoxia, compared to controls. Treatment with esomeprazole or lansoprazole in vitro increased placental LOX-1 expression. LOX-1 expression is reduced in preeclamptic placentas and hypoxic cytotrophoblast. Esomeprazole and lansoprazole increase placental LOX-1 expression. These findings demonstrate a role for LOX-1 in the placenta, and improve our understanding of maternal adaptations in pregnancy complications.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2210778921003172; http://dx.doi.org/10.1016/j.preghy.2021.07.243; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85111212193&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/34325289; https://linkinghub.elsevier.com/retrieve/pii/S2210778921003172; https://dx.doi.org/10.1016/j.preghy.2021.07.243
Elsevier BV
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