Role of Elevated SFLT‐1 on the Regulation of Placental Transporters in Women With Pre‐Eclampsia
Pre‐eclampsia (PE) is an obstetric complication associated with elevated levels of fms‐like tyrosine kinase 1 (sFlt‐1) and dysregulated trophoblast differentiation. However, limited information exists on the expression and regulation of placental drug transporters in PE. Transporter mRNA and protein...
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2020-05-01
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Online Access: | https://doi.org/10.1111/cts.12742 |
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doaj-62e46cb3e0794dd783aa4b42cb2c72252020-11-25T02:59:24ZengWileyClinical and Translational Science1752-80541752-80622020-05-0113358058810.1111/cts.12742Role of Elevated SFLT‐1 on the Regulation of Placental Transporters in Women With Pre‐EclampsiaDea Kojovic0Natalie V. Workewych1Micheline Piquette‐Miller2Leslie Dan Faculty of Pharmacy University of Toronto Toronto Ontario CanadaDepartment of Pharmacology and Toxicology Faculty of Medicine University of Toronto Toronto Ontario CanadaLeslie Dan Faculty of Pharmacy University of Toronto Toronto Ontario CanadaPre‐eclampsia (PE) is an obstetric complication associated with elevated levels of fms‐like tyrosine kinase 1 (sFlt‐1) and dysregulated trophoblast differentiation. However, limited information exists on the expression and regulation of placental drug transporters in PE. Transporter mRNA and protein expression were analyzed in human placentas diagnosed with PE (n = 34) and gestational age‐matched controls (n = 24), whereas placental BeWo cells were treated with angiogenic factors in vitro. Significant downregulation of breast cancer resistance protein (BCRP) and several other transporters were seen in placentas complicated by PE compared with controls, whereas mRNA levels of sFlt‐1 were induced by 2.5‐fold in PE placentas (P < 0.01). Treatment of BeWo cells with sFlt‐1 resulted in an 85–90% downregulation of BCRP, which was attenuated by vascular endothelial growth factor. Our findings suggest that placental function is compromised during PE due to altered expression of clinically important transporters. Furthermore, our in vitro results show that sFlt‐1 is involved in the regulation of BCRP.https://doi.org/10.1111/cts.12742 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Dea Kojovic Natalie V. Workewych Micheline Piquette‐Miller |
spellingShingle |
Dea Kojovic Natalie V. Workewych Micheline Piquette‐Miller Role of Elevated SFLT‐1 on the Regulation of Placental Transporters in Women With Pre‐Eclampsia Clinical and Translational Science |
author_facet |
Dea Kojovic Natalie V. Workewych Micheline Piquette‐Miller |
author_sort |
Dea Kojovic |
title |
Role of Elevated SFLT‐1 on the Regulation of Placental Transporters in Women With Pre‐Eclampsia |
title_short |
Role of Elevated SFLT‐1 on the Regulation of Placental Transporters in Women With Pre‐Eclampsia |
title_full |
Role of Elevated SFLT‐1 on the Regulation of Placental Transporters in Women With Pre‐Eclampsia |
title_fullStr |
Role of Elevated SFLT‐1 on the Regulation of Placental Transporters in Women With Pre‐Eclampsia |
title_full_unstemmed |
Role of Elevated SFLT‐1 on the Regulation of Placental Transporters in Women With Pre‐Eclampsia |
title_sort |
role of elevated sflt‐1 on the regulation of placental transporters in women with pre‐eclampsia |
publisher |
Wiley |
series |
Clinical and Translational Science |
issn |
1752-8054 1752-8062 |
publishDate |
2020-05-01 |
description |
Pre‐eclampsia (PE) is an obstetric complication associated with elevated levels of fms‐like tyrosine kinase 1 (sFlt‐1) and dysregulated trophoblast differentiation. However, limited information exists on the expression and regulation of placental drug transporters in PE. Transporter mRNA and protein expression were analyzed in human placentas diagnosed with PE (n = 34) and gestational age‐matched controls (n = 24), whereas placental BeWo cells were treated with angiogenic factors in vitro. Significant downregulation of breast cancer resistance protein (BCRP) and several other transporters were seen in placentas complicated by PE compared with controls, whereas mRNA levels of sFlt‐1 were induced by 2.5‐fold in PE placentas (P < 0.01). Treatment of BeWo cells with sFlt‐1 resulted in an 85–90% downregulation of BCRP, which was attenuated by vascular endothelial growth factor. Our findings suggest that placental function is compromised during PE due to altered expression of clinically important transporters. Furthermore, our in vitro results show that sFlt‐1 is involved in the regulation of BCRP. |
url |
https://doi.org/10.1111/cts.12742 |
work_keys_str_mv |
AT deakojovic roleofelevatedsflt1ontheregulationofplacentaltransportersinwomenwithpreeclampsia AT natalievworkewych roleofelevatedsflt1ontheregulationofplacentaltransportersinwomenwithpreeclampsia AT michelinepiquettemiller roleofelevatedsflt1ontheregulationofplacentaltransportersinwomenwithpreeclampsia |
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