Increased maternal and fetal cholesterol efflux capacity and placental cyp27a1 expression in pre-eclampsia

Preeclampsia is a pregnancy-specific condition that leads to increased cardiovascular risk in later life. A decrease in cholesterol efflux capacity is linked to CVD. We hypothesized that in preeclampsia there would be a disruption of maternal/fetal plasma to efflux cholesterol, as well as difference...

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Main Authors: Mistry, Hiten D., Kurlak, L.O., Mansour, Yosef, Zurkinden, Line, Mohaupt, Markus, Escher, Genevieve
Format: Article
Published: American Society for Biochemistry and Molecular Biology 2017
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Online Access:https://eprints.nottingham.ac.uk/44336/
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author Mistry, Hiten D.
Kurlak, L.O.
Mansour, Yosef
Zurkinden, Line
Mohaupt, Markus
Escher, Genevieve
author_facet Mistry, Hiten D.
Kurlak, L.O.
Mansour, Yosef
Zurkinden, Line
Mohaupt, Markus
Escher, Genevieve
author_sort Mistry, Hiten D.
building Nottingham Research Data Repository
collection Online Access
description Preeclampsia is a pregnancy-specific condition that leads to increased cardiovascular risk in later life. A decrease in cholesterol efflux capacity is linked to CVD. We hypothesized that in preeclampsia there would be a disruption of maternal/fetal plasma to efflux cholesterol, as well as differences in the concentrations of both placental sterol 27-hydroxylase (CYP27A1) and apoA1 binding protein (AIBP). Total, HDL-, and ABCA1-mediated cholesterol effluxes were performed with maternal and fetal plasma from women with preeclampsia and normotensive controls (both n = 17). apoA1 and apoE were quantified by chemiluminescence, and 27-hydroxycholesterol (27-OHC) by GC-MS. Immunohistochemistry was used to determine placental expression/localization of CYP27A1, AIBP, apoA1, apoE, and SRB1. Maternal and fetal total and HDL-mediated cholesterol efflux capacities were increased in preeclampsia (by 10–20%), but ABCA1-mediated efflux was decreased (by 20–35%; P < 0.05). Maternal and fetal apoE concentrations were higher in preeclampsia. Fetal plasma 27-OHC levels were decreased in preeclamptic samples (P < 0.05). Placental protein expression of both CYP27A1 and AIBP were localized around fetal vessels and significantly increased in preeclampsia (P = 0.04). Placental 27-OHC concentrations were also raised in preeclampsia (P < 0.05). Increased HDL-mediated cholesterol efflux capacity and placental CYP27A1/27-OHC could be a rescue mechanism in preeclampsia, to remove cholesterol from cells to limit lipid peroxidation and increase placental angiogenesis.
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spelling nottingham-443362020-05-04T18:49:28Z https://eprints.nottingham.ac.uk/44336/ Increased maternal and fetal cholesterol efflux capacity and placental cyp27a1 expression in pre-eclampsia Mistry, Hiten D. Kurlak, L.O. Mansour, Yosef Zurkinden, Line Mohaupt, Markus Escher, Genevieve Preeclampsia is a pregnancy-specific condition that leads to increased cardiovascular risk in later life. A decrease in cholesterol efflux capacity is linked to CVD. We hypothesized that in preeclampsia there would be a disruption of maternal/fetal plasma to efflux cholesterol, as well as differences in the concentrations of both placental sterol 27-hydroxylase (CYP27A1) and apoA1 binding protein (AIBP). Total, HDL-, and ABCA1-mediated cholesterol effluxes were performed with maternal and fetal plasma from women with preeclampsia and normotensive controls (both n = 17). apoA1 and apoE were quantified by chemiluminescence, and 27-hydroxycholesterol (27-OHC) by GC-MS. Immunohistochemistry was used to determine placental expression/localization of CYP27A1, AIBP, apoA1, apoE, and SRB1. Maternal and fetal total and HDL-mediated cholesterol efflux capacities were increased in preeclampsia (by 10–20%), but ABCA1-mediated efflux was decreased (by 20–35%; P < 0.05). Maternal and fetal apoE concentrations were higher in preeclampsia. Fetal plasma 27-OHC levels were decreased in preeclamptic samples (P < 0.05). Placental protein expression of both CYP27A1 and AIBP were localized around fetal vessels and significantly increased in preeclampsia (P = 0.04). Placental 27-OHC concentrations were also raised in preeclampsia (P < 0.05). Increased HDL-mediated cholesterol efflux capacity and placental CYP27A1/27-OHC could be a rescue mechanism in preeclampsia, to remove cholesterol from cells to limit lipid peroxidation and increase placental angiogenesis. American Society for Biochemistry and Molecular Biology 2017-06-10 Article PeerReviewed Mistry, Hiten D., Kurlak, L.O., Mansour, Yosef, Zurkinden, Line, Mohaupt, Markus and Escher, Genevieve (2017) Increased maternal and fetal cholesterol efflux capacity and placental cyp27a1 expression in pre-eclampsia. Journal of Lipid Research, 58 . pp. 1186-1185. ISSN 1539-7262 lipid/efflux; 27-hydroxycholesterol; apolipoproteins; pregnancy; hypertension; sterol 27-hydroxylase http://www.jlr.org/content/58/6/1186.short doi:10.1194/jlr.M071985 doi:10.1194/jlr.M071985
spellingShingle lipid/efflux; 27-hydroxycholesterol; apolipoproteins; pregnancy; hypertension; sterol 27-hydroxylase
Mistry, Hiten D.
Kurlak, L.O.
Mansour, Yosef
Zurkinden, Line
Mohaupt, Markus
Escher, Genevieve
Increased maternal and fetal cholesterol efflux capacity and placental cyp27a1 expression in pre-eclampsia
title Increased maternal and fetal cholesterol efflux capacity and placental cyp27a1 expression in pre-eclampsia
title_full Increased maternal and fetal cholesterol efflux capacity and placental cyp27a1 expression in pre-eclampsia
title_fullStr Increased maternal and fetal cholesterol efflux capacity and placental cyp27a1 expression in pre-eclampsia
title_full_unstemmed Increased maternal and fetal cholesterol efflux capacity and placental cyp27a1 expression in pre-eclampsia
title_short Increased maternal and fetal cholesterol efflux capacity and placental cyp27a1 expression in pre-eclampsia
title_sort increased maternal and fetal cholesterol efflux capacity and placental cyp27a1 expression in pre-eclampsia
topic lipid/efflux; 27-hydroxycholesterol; apolipoproteins; pregnancy; hypertension; sterol 27-hydroxylase
url https://eprints.nottingham.ac.uk/44336/
https://eprints.nottingham.ac.uk/44336/
https://eprints.nottingham.ac.uk/44336/