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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Main Authors: Dea Kojovic, Natalie V. Workewych, Micheline Piquette‐Miller
Format: Article
Language:English
Published: Wiley 2020-05-01
Series:Clinical and Translational Science
Online Access:https://doi.org/10.1111/cts.12742
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spelling 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
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