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Canonical, Non-Canonical and Atypical Pathways of Nuclear Factor кb Activation in Preeclampsia
Although higher nuclear factor κB (NFκB) expression and activity is observed in preeclamptic placentas, its mechanism of activation is unknown. This is the first study to investigate whether the canonical, non-canonical, or atypical NFκB activation pathways may be responsible for the higher activati...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432517/ https://www.ncbi.nlm.nih.gov/pubmed/32759710 http://dx.doi.org/10.3390/ijms21155574 |
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author | Sakowicz, Agata Bralewska, Michalina Pietrucha, Tadeusz Habrowska-Górczyńska, Dominika E Piastowska-Ciesielska, Agnieszka W Gach, Agnieszka Rybak-Krzyszkowska, Magda Witas, Piotr J Huras, Hubert Grzesiak, Mariusz Biesiada, Lidia |
author_facet | Sakowicz, Agata Bralewska, Michalina Pietrucha, Tadeusz Habrowska-Górczyńska, Dominika E Piastowska-Ciesielska, Agnieszka W Gach, Agnieszka Rybak-Krzyszkowska, Magda Witas, Piotr J Huras, Hubert Grzesiak, Mariusz Biesiada, Lidia |
author_sort | Sakowicz, Agata |
collection | PubMed |
description | Although higher nuclear factor κB (NFκB) expression and activity is observed in preeclamptic placentas, its mechanism of activation is unknown. This is the first study to investigate whether the canonical, non-canonical, or atypical NFκB activation pathways may be responsible for the higher activation of NFκB observed in preeclamptic placentas. The study included 268 cases (130 preeclamptic women and 138 controls). We studied the expression of the genes coding for NFκB activators (NIK, IKKα, IKKβ, and CK2α) and inhibitors (IκBα and IκBβ) using RT-PCR in real time. The RT-PCR results were verified on the protein level using ELISA and Western blot. To determine the efficiency of the pathways, the ratios of activator(s) to one of the inhibitors (IκBα or IκBβ) were calculated for each studied pathway. The preeclamptic placentas demonstrated significantly lower IKKα and CK2α but higher IκBα and IκBβ protein levels. In addition, the calculated activator(s) to inhibitor (IκBα or IκBβ) ratios suggested that all studied pathways might be downregulated in preeclamptic placentas. Our results indicate that preeclamptic placentas may demonstrate mechanisms of NFκB activation other than the canonical, non-canonical, and atypical forms. In these mechanisms, inhibitors of NFκB may play a key role. These observations broaden the existing knowledge regarding the molecular background of preeclampsia development. |
format | Online Article Text |
id | pubmed-7432517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74325172020-08-24 Canonical, Non-Canonical and Atypical Pathways of Nuclear Factor кb Activation in Preeclampsia Sakowicz, Agata Bralewska, Michalina Pietrucha, Tadeusz Habrowska-Górczyńska, Dominika E Piastowska-Ciesielska, Agnieszka W Gach, Agnieszka Rybak-Krzyszkowska, Magda Witas, Piotr J Huras, Hubert Grzesiak, Mariusz Biesiada, Lidia Int J Mol Sci Article Although higher nuclear factor κB (NFκB) expression and activity is observed in preeclamptic placentas, its mechanism of activation is unknown. This is the first study to investigate whether the canonical, non-canonical, or atypical NFκB activation pathways may be responsible for the higher activation of NFκB observed in preeclamptic placentas. The study included 268 cases (130 preeclamptic women and 138 controls). We studied the expression of the genes coding for NFκB activators (NIK, IKKα, IKKβ, and CK2α) and inhibitors (IκBα and IκBβ) using RT-PCR in real time. The RT-PCR results were verified on the protein level using ELISA and Western blot. To determine the efficiency of the pathways, the ratios of activator(s) to one of the inhibitors (IκBα or IκBβ) were calculated for each studied pathway. The preeclamptic placentas demonstrated significantly lower IKKα and CK2α but higher IκBα and IκBβ protein levels. In addition, the calculated activator(s) to inhibitor (IκBα or IκBβ) ratios suggested that all studied pathways might be downregulated in preeclamptic placentas. Our results indicate that preeclamptic placentas may demonstrate mechanisms of NFκB activation other than the canonical, non-canonical, and atypical forms. In these mechanisms, inhibitors of NFκB may play a key role. These observations broaden the existing knowledge regarding the molecular background of preeclampsia development. MDPI 2020-08-04 /pmc/articles/PMC7432517/ /pubmed/32759710 http://dx.doi.org/10.3390/ijms21155574 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sakowicz, Agata Bralewska, Michalina Pietrucha, Tadeusz Habrowska-Górczyńska, Dominika E Piastowska-Ciesielska, Agnieszka W Gach, Agnieszka Rybak-Krzyszkowska, Magda Witas, Piotr J Huras, Hubert Grzesiak, Mariusz Biesiada, Lidia Canonical, Non-Canonical and Atypical Pathways of Nuclear Factor кb Activation in Preeclampsia |
title | Canonical, Non-Canonical and Atypical Pathways of Nuclear Factor кb Activation in Preeclampsia |
title_full | Canonical, Non-Canonical and Atypical Pathways of Nuclear Factor кb Activation in Preeclampsia |
title_fullStr | Canonical, Non-Canonical and Atypical Pathways of Nuclear Factor кb Activation in Preeclampsia |
title_full_unstemmed | Canonical, Non-Canonical and Atypical Pathways of Nuclear Factor кb Activation in Preeclampsia |
title_short | Canonical, Non-Canonical and Atypical Pathways of Nuclear Factor кb Activation in Preeclampsia |
title_sort | canonical, non-canonical and atypical pathways of nuclear factor кb activation in preeclampsia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432517/ https://www.ncbi.nlm.nih.gov/pubmed/32759710 http://dx.doi.org/10.3390/ijms21155574 |
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