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Expression of ABCA1 Transporter and LXRA/LXRB Receptors in Placenta of Women with Late Onset Preeclampsia
Background: Appropriate levels of cholesterol are necessary for the mother and developing fetus, but theirexcess may cause preeclampsia. The ABCA1 transporter mediates the secretion of cholesterol and is highly regulated at the transcriptional level via the nuclear liver X receptors (LXRs). Methods:...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410380/ https://www.ncbi.nlm.nih.gov/pubmed/36013052 http://dx.doi.org/10.3390/jcm11164809 |
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author | Wolski, Hubert Ożarowski, Marcin Kurzawińska, Grażyna Bogacz, Anna Wolek, Marlena Łuszczyńska, Małgorzata Drews, Krzysztof Mrozikiewicz, Aleksandra E. Mikołajczak, Przemysław Ł. Kujawski, Radosław Czerny, Bogusław Karpiński, Tomasz M. Seremak-Mrozikiewicz, Agnieszka |
author_facet | Wolski, Hubert Ożarowski, Marcin Kurzawińska, Grażyna Bogacz, Anna Wolek, Marlena Łuszczyńska, Małgorzata Drews, Krzysztof Mrozikiewicz, Aleksandra E. Mikołajczak, Przemysław Ł. Kujawski, Radosław Czerny, Bogusław Karpiński, Tomasz M. Seremak-Mrozikiewicz, Agnieszka |
author_sort | Wolski, Hubert |
collection | PubMed |
description | Background: Appropriate levels of cholesterol are necessary for the mother and developing fetus, but theirexcess may cause preeclampsia. The ABCA1 transporter mediates the secretion of cholesterol and is highly regulated at the transcriptional level via the nuclear liver X receptors (LXRs). Methods: Sixteen preeclamptic and 39 normotensives healthy women with uncomplicated pregnancies were involved in the case-control study. The placental levels of ABCA1, LXRA and LXRB mRNA were quantified by real-time quantitative PCR. The concentrations of ABCA1, LXRA and LXRB proteins from the placenta were determined using an enzyme-linked immunosorbent assay Results: We found in the logistic regression model significantly lower placental expression of LXRB mRNA (crude OR = 0.26, 95% CI: 0.07–0.94, p = 0.040) and LXRA protein level (crude OR = 0.19, 95% CI: 0.05–0.69, p = 0.012) in late-onset preeclamptic women compared to healthy pregnant women. The values remained statistically significant after adjustment for possible confounders. Conclusions: Our results suggest that high placenta LXRA mRNA and LXRA protein expression levels decrease the risk of late-onset preeclampsia. These nuclear receptors could play a role in the development of preeclampsia through disturbances of lipid metabolism. |
format | Online Article Text |
id | pubmed-9410380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94103802022-08-26 Expression of ABCA1 Transporter and LXRA/LXRB Receptors in Placenta of Women with Late Onset Preeclampsia Wolski, Hubert Ożarowski, Marcin Kurzawińska, Grażyna Bogacz, Anna Wolek, Marlena Łuszczyńska, Małgorzata Drews, Krzysztof Mrozikiewicz, Aleksandra E. Mikołajczak, Przemysław Ł. Kujawski, Radosław Czerny, Bogusław Karpiński, Tomasz M. Seremak-Mrozikiewicz, Agnieszka J Clin Med Article Background: Appropriate levels of cholesterol are necessary for the mother and developing fetus, but theirexcess may cause preeclampsia. The ABCA1 transporter mediates the secretion of cholesterol and is highly regulated at the transcriptional level via the nuclear liver X receptors (LXRs). Methods: Sixteen preeclamptic and 39 normotensives healthy women with uncomplicated pregnancies were involved in the case-control study. The placental levels of ABCA1, LXRA and LXRB mRNA were quantified by real-time quantitative PCR. The concentrations of ABCA1, LXRA and LXRB proteins from the placenta were determined using an enzyme-linked immunosorbent assay Results: We found in the logistic regression model significantly lower placental expression of LXRB mRNA (crude OR = 0.26, 95% CI: 0.07–0.94, p = 0.040) and LXRA protein level (crude OR = 0.19, 95% CI: 0.05–0.69, p = 0.012) in late-onset preeclamptic women compared to healthy pregnant women. The values remained statistically significant after adjustment for possible confounders. Conclusions: Our results suggest that high placenta LXRA mRNA and LXRA protein expression levels decrease the risk of late-onset preeclampsia. These nuclear receptors could play a role in the development of preeclampsia through disturbances of lipid metabolism. MDPI 2022-08-17 /pmc/articles/PMC9410380/ /pubmed/36013052 http://dx.doi.org/10.3390/jcm11164809 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wolski, Hubert Ożarowski, Marcin Kurzawińska, Grażyna Bogacz, Anna Wolek, Marlena Łuszczyńska, Małgorzata Drews, Krzysztof Mrozikiewicz, Aleksandra E. Mikołajczak, Przemysław Ł. Kujawski, Radosław Czerny, Bogusław Karpiński, Tomasz M. Seremak-Mrozikiewicz, Agnieszka Expression of ABCA1 Transporter and LXRA/LXRB Receptors in Placenta of Women with Late Onset Preeclampsia |
title | Expression of ABCA1 Transporter and LXRA/LXRB Receptors in Placenta of Women with Late Onset Preeclampsia |
title_full | Expression of ABCA1 Transporter and LXRA/LXRB Receptors in Placenta of Women with Late Onset Preeclampsia |
title_fullStr | Expression of ABCA1 Transporter and LXRA/LXRB Receptors in Placenta of Women with Late Onset Preeclampsia |
title_full_unstemmed | Expression of ABCA1 Transporter and LXRA/LXRB Receptors in Placenta of Women with Late Onset Preeclampsia |
title_short | Expression of ABCA1 Transporter and LXRA/LXRB Receptors in Placenta of Women with Late Onset Preeclampsia |
title_sort | expression of abca1 transporter and lxra/lxrb receptors in placenta of women with late onset preeclampsia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410380/ https://www.ncbi.nlm.nih.gov/pubmed/36013052 http://dx.doi.org/10.3390/jcm11164809 |
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