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Anti-Apoptotic Effect of Apelin in Human Placenta: Studies on BeWo Cells and Villous Explants from Third-Trimester Human Pregnancy

Previously, we demonstrated the expression of apelin and G-protein-coupled receptor APJ in human placenta cell lines as well as its direct action on placenta cell proliferation and endocrinology. The objective of this study was to examine the effect of apelin on placenta apoptosis in BeWo cells and...

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Autores principales: Mlyczyńska, Ewa, Myszka, Małgorzata, Kurowska, Patrycja, Dawid, Monika, Milewicz, Tomasz, Bałajewicz-Nowak, Marta, Kowalczyk, Paweł, Rak, Agnieszka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7967155/
https://www.ncbi.nlm.nih.gov/pubmed/33803239
http://dx.doi.org/10.3390/ijms22052760
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author Mlyczyńska, Ewa
Myszka, Małgorzata
Kurowska, Patrycja
Dawid, Monika
Milewicz, Tomasz
Bałajewicz-Nowak, Marta
Kowalczyk, Paweł
Rak, Agnieszka
author_facet Mlyczyńska, Ewa
Myszka, Małgorzata
Kurowska, Patrycja
Dawid, Monika
Milewicz, Tomasz
Bałajewicz-Nowak, Marta
Kowalczyk, Paweł
Rak, Agnieszka
author_sort Mlyczyńska, Ewa
collection PubMed
description Previously, we demonstrated the expression of apelin and G-protein-coupled receptor APJ in human placenta cell lines as well as its direct action on placenta cell proliferation and endocrinology. The objective of this study was to examine the effect of apelin on placenta apoptosis in BeWo cells and villous explants from the human third trimester of pregnancy. The BeWo cells and villous explants were incubated with apelin (2 and 20 ng/mL) alone or with staurosporine for 24 to 72 h. First, we analysed the dose- and time-dependent effect of apelin on the expression of apoptotic factors on the mRNA level by real-time PCR and on the protein level using Western blot. Next, we checked caspase 3 and 7 activity by Caspase-Glo 3/7, DNA fragmentation by the Cell Death Detection ELISA kit and oxygen consumption by the MitoXpress-Xtra Oxygen Consumption assay. We found that apelin increased the expression of pro-survival and decreased proapoptotic factors on mRNA and protein levels in both BeWo cells and villous explants. Additionally, apelin inhibited caspase 3 and 7 activity and DNA fragmentation in staurosporine-induced apoptosis as also attenuated oxidative stress by increasing extracellular oxygen consumption. The antiapoptotic effect of apelin in BeWo cells was mediated by the APJ receptor and mitogen-activated protein kinase (ERK1/2/MAP3/1) and protein kinase B (AKT). The obtained results showed the antiapoptotic effect of apelin on trophoblast cells, suggesting its participation in the development of the placenta.
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spelling pubmed-79671552021-03-18 Anti-Apoptotic Effect of Apelin in Human Placenta: Studies on BeWo Cells and Villous Explants from Third-Trimester Human Pregnancy Mlyczyńska, Ewa Myszka, Małgorzata Kurowska, Patrycja Dawid, Monika Milewicz, Tomasz Bałajewicz-Nowak, Marta Kowalczyk, Paweł Rak, Agnieszka Int J Mol Sci Article Previously, we demonstrated the expression of apelin and G-protein-coupled receptor APJ in human placenta cell lines as well as its direct action on placenta cell proliferation and endocrinology. The objective of this study was to examine the effect of apelin on placenta apoptosis in BeWo cells and villous explants from the human third trimester of pregnancy. The BeWo cells and villous explants were incubated with apelin (2 and 20 ng/mL) alone or with staurosporine for 24 to 72 h. First, we analysed the dose- and time-dependent effect of apelin on the expression of apoptotic factors on the mRNA level by real-time PCR and on the protein level using Western blot. Next, we checked caspase 3 and 7 activity by Caspase-Glo 3/7, DNA fragmentation by the Cell Death Detection ELISA kit and oxygen consumption by the MitoXpress-Xtra Oxygen Consumption assay. We found that apelin increased the expression of pro-survival and decreased proapoptotic factors on mRNA and protein levels in both BeWo cells and villous explants. Additionally, apelin inhibited caspase 3 and 7 activity and DNA fragmentation in staurosporine-induced apoptosis as also attenuated oxidative stress by increasing extracellular oxygen consumption. The antiapoptotic effect of apelin in BeWo cells was mediated by the APJ receptor and mitogen-activated protein kinase (ERK1/2/MAP3/1) and protein kinase B (AKT). The obtained results showed the antiapoptotic effect of apelin on trophoblast cells, suggesting its participation in the development of the placenta. MDPI 2021-03-09 /pmc/articles/PMC7967155/ /pubmed/33803239 http://dx.doi.org/10.3390/ijms22052760 Text en © 2021 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
Mlyczyńska, Ewa
Myszka, Małgorzata
Kurowska, Patrycja
Dawid, Monika
Milewicz, Tomasz
Bałajewicz-Nowak, Marta
Kowalczyk, Paweł
Rak, Agnieszka
Anti-Apoptotic Effect of Apelin in Human Placenta: Studies on BeWo Cells and Villous Explants from Third-Trimester Human Pregnancy
title Anti-Apoptotic Effect of Apelin in Human Placenta: Studies on BeWo Cells and Villous Explants from Third-Trimester Human Pregnancy
title_full Anti-Apoptotic Effect of Apelin in Human Placenta: Studies on BeWo Cells and Villous Explants from Third-Trimester Human Pregnancy
title_fullStr Anti-Apoptotic Effect of Apelin in Human Placenta: Studies on BeWo Cells and Villous Explants from Third-Trimester Human Pregnancy
title_full_unstemmed Anti-Apoptotic Effect of Apelin in Human Placenta: Studies on BeWo Cells and Villous Explants from Third-Trimester Human Pregnancy
title_short Anti-Apoptotic Effect of Apelin in Human Placenta: Studies on BeWo Cells and Villous Explants from Third-Trimester Human Pregnancy
title_sort anti-apoptotic effect of apelin in human placenta: studies on bewo cells and villous explants from third-trimester human pregnancy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7967155/
https://www.ncbi.nlm.nih.gov/pubmed/33803239
http://dx.doi.org/10.3390/ijms22052760
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