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Sex-dependent dysregulation of human neutrophil responses by bisphenol A
BACKGROUND: In the present study, we aimed to investigate selected functions of human neutrophils exposed to bisphenol A (BPA) under in vitro conditions. As BPA is classified among xenoestrogens, we compared its action and effects with those of 17β-estradiol (E2). METHODS: Chemotaxis of neutrophils...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791670/ https://www.ncbi.nlm.nih.gov/pubmed/33413436 http://dx.doi.org/10.1186/s12940-020-00686-8 |
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author | Ratajczak-Wrona, Wioletta Garley, Marzena Rusak, Malgorzata Nowak, Karolina Czerniecki, Jan Wolosewicz, Katarzyna Dabrowska, Milena Wolczynski, Slawomir Radziwon, Piotr Jablonska, Ewa |
author_facet | Ratajczak-Wrona, Wioletta Garley, Marzena Rusak, Malgorzata Nowak, Karolina Czerniecki, Jan Wolosewicz, Katarzyna Dabrowska, Milena Wolczynski, Slawomir Radziwon, Piotr Jablonska, Ewa |
author_sort | Ratajczak-Wrona, Wioletta |
collection | PubMed |
description | BACKGROUND: In the present study, we aimed to investigate selected functions of human neutrophils exposed to bisphenol A (BPA) under in vitro conditions. As BPA is classified among xenoestrogens, we compared its action and effects with those of 17β-estradiol (E2). METHODS: Chemotaxis of neutrophils was examined using the Boyden chamber. Their phagocytosis and nicotinamide adenine dinucleotide phosphate hydrogen (NADPH) oxidase activity were assessed via Park’s method with latex beads and Park’s test with nitroblue tetrazolium. To assess the total concentration of nitric oxide (NO), the Griess reaction was utilized. Flow cytometry was used to assess the expression of cluster of differentiation (CD) antigens. The formation of neutrophil extracellular traps (NETs) was analyzed using a microscope (IN Cell Analyzer 2200 system). Expression of the investigated proteins was determined using Western blot. RESULTS: The analysis of results obtained for both sexes demonstrated that after exposure to BPA, the chemotactic capacity of neutrophils was reduced. In the presence of BPA, the phagocytic activity was found to be elevated in the cells obtained from women and reduced in the cells from men. Following exposure to BPA, the percentage of neutrophils with CD14 and CD284 (TLR4) expression, as well as the percentage of cells forming NETs, was increased in the cells from both sexes. The stimulatory role of BPA and E2 in the activation of NADPH oxidase was observed only in female cells. On the other hand, no influence of E2 on the expression of CD14 and CD284, chemotaxis, phagocytosis, and the amount of NET-positive neutrophils was found for both sexes. The study further showed that BPA intensified NO production and iNOS expression in the cells of both sexes. In addition, intensified expression of all tested PI3K-Akt pathway proteins was observed in male neutrophils. CONCLUSIONS: The study demonstrated the influence of BPA on neutrophil functions associated with locomotion and pathogen elimination, which in turn may disturb the immune response of these cells in both women and men. Analysis of the obtained data showed that the effect of this xenoestrogen on the human neutrophils was more pronounced than E2. |
format | Online Article Text |
id | pubmed-7791670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77916702021-01-11 Sex-dependent dysregulation of human neutrophil responses by bisphenol A Ratajczak-Wrona, Wioletta Garley, Marzena Rusak, Malgorzata Nowak, Karolina Czerniecki, Jan Wolosewicz, Katarzyna Dabrowska, Milena Wolczynski, Slawomir Radziwon, Piotr Jablonska, Ewa Environ Health Research BACKGROUND: In the present study, we aimed to investigate selected functions of human neutrophils exposed to bisphenol A (BPA) under in vitro conditions. As BPA is classified among xenoestrogens, we compared its action and effects with those of 17β-estradiol (E2). METHODS: Chemotaxis of neutrophils was examined using the Boyden chamber. Their phagocytosis and nicotinamide adenine dinucleotide phosphate hydrogen (NADPH) oxidase activity were assessed via Park’s method with latex beads and Park’s test with nitroblue tetrazolium. To assess the total concentration of nitric oxide (NO), the Griess reaction was utilized. Flow cytometry was used to assess the expression of cluster of differentiation (CD) antigens. The formation of neutrophil extracellular traps (NETs) was analyzed using a microscope (IN Cell Analyzer 2200 system). Expression of the investigated proteins was determined using Western blot. RESULTS: The analysis of results obtained for both sexes demonstrated that after exposure to BPA, the chemotactic capacity of neutrophils was reduced. In the presence of BPA, the phagocytic activity was found to be elevated in the cells obtained from women and reduced in the cells from men. Following exposure to BPA, the percentage of neutrophils with CD14 and CD284 (TLR4) expression, as well as the percentage of cells forming NETs, was increased in the cells from both sexes. The stimulatory role of BPA and E2 in the activation of NADPH oxidase was observed only in female cells. On the other hand, no influence of E2 on the expression of CD14 and CD284, chemotaxis, phagocytosis, and the amount of NET-positive neutrophils was found for both sexes. The study further showed that BPA intensified NO production and iNOS expression in the cells of both sexes. In addition, intensified expression of all tested PI3K-Akt pathway proteins was observed in male neutrophils. CONCLUSIONS: The study demonstrated the influence of BPA on neutrophil functions associated with locomotion and pathogen elimination, which in turn may disturb the immune response of these cells in both women and men. Analysis of the obtained data showed that the effect of this xenoestrogen on the human neutrophils was more pronounced than E2. BioMed Central 2021-01-07 /pmc/articles/PMC7791670/ /pubmed/33413436 http://dx.doi.org/10.1186/s12940-020-00686-8 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ratajczak-Wrona, Wioletta Garley, Marzena Rusak, Malgorzata Nowak, Karolina Czerniecki, Jan Wolosewicz, Katarzyna Dabrowska, Milena Wolczynski, Slawomir Radziwon, Piotr Jablonska, Ewa Sex-dependent dysregulation of human neutrophil responses by bisphenol A |
title | Sex-dependent dysregulation of human neutrophil responses by bisphenol A |
title_full | Sex-dependent dysregulation of human neutrophil responses by bisphenol A |
title_fullStr | Sex-dependent dysregulation of human neutrophil responses by bisphenol A |
title_full_unstemmed | Sex-dependent dysregulation of human neutrophil responses by bisphenol A |
title_short | Sex-dependent dysregulation of human neutrophil responses by bisphenol A |
title_sort | sex-dependent dysregulation of human neutrophil responses by bisphenol a |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791670/ https://www.ncbi.nlm.nih.gov/pubmed/33413436 http://dx.doi.org/10.1186/s12940-020-00686-8 |
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