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Nickel oxide nanoparticles can recruit eosinophils in the lungs of rats by the direct release of intracellular eotaxin

BACKGROUND: Instillation of highly soluble nanoparticles (NPs) into the lungs of rodents can cause acute eosinophilia without any previous sensitizations by the role of dissolved ions. However, whether gradually dissolving NPs can cause the same type of eosinophilia remains to be elucidated. We sele...

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Autores principales: Lee, Seonghan, Hwang, Sung-Hyun, Jeong, Jiyoung, Han, Youngju, Kim, Sung-Hyun, Lee, Dong-Keon, Lee, Hae-Suk, Chung, Seung-Tae, Jeong, Jayoung, Roh, Changhyun, Huh, Yun Seok, Cho, Wan-Seob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899890/
https://www.ncbi.nlm.nih.gov/pubmed/27283431
http://dx.doi.org/10.1186/s12989-016-0142-8
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author Lee, Seonghan
Hwang, Sung-Hyun
Jeong, Jiyoung
Han, Youngju
Kim, Sung-Hyun
Lee, Dong-Keon
Lee, Hae-Suk
Chung, Seung-Tae
Jeong, Jayoung
Roh, Changhyun
Huh, Yun Seok
Cho, Wan-Seob
author_facet Lee, Seonghan
Hwang, Sung-Hyun
Jeong, Jiyoung
Han, Youngju
Kim, Sung-Hyun
Lee, Dong-Keon
Lee, Hae-Suk
Chung, Seung-Tae
Jeong, Jayoung
Roh, Changhyun
Huh, Yun Seok
Cho, Wan-Seob
author_sort Lee, Seonghan
collection PubMed
description BACKGROUND: Instillation of highly soluble nanoparticles (NPs) into the lungs of rodents can cause acute eosinophilia without any previous sensitizations by the role of dissolved ions. However, whether gradually dissolving NPs can cause the same type of eosinophilia remains to be elucidated. We selected nickel oxide (NiO) as a gradually dissolving NP and evaluated the time course pulmonary inflammation pattern as well as its mechanisms. METHODS: NiO NPs were intratracheally instilled into female Wistar rats at various concentrations (50, 100, and 200 cm(2)/rat) and the lung inflammation was evaluated at various time-points (1, 2, 3, and 4 days). As positive controls, NiCl(2) and the ovalbumin-induced allergic airway inflammation model was applied. NiCl(2) was instilled at 171.1 μg Ni/rat, which is equivalent nickel concentration of 200 cm(2)/rat of NiO NPs. Cytological analysis and biochemical analysis including lactate dehydrogenase (LDH), total protein, and pro-inflammatory cytokines were measured in bronchoalveolar lavage fluid (BALF). The levels of total immunoglobulin E (IgE) and anaphylatoxins (C3a and C5a) were measured in BALF and serum. The levels of eotaxin were measured in the alveolar macrophages and normal lung tissue before and after addition of cell lysis buffer to evaluate whether the direct lysis of cells can release intracellular eotaxin. RESULTS: NiO NPs produced acute neutrophilic inflammation throughout the study. However, eosinophils were recruited at 3 and 4 days post-instillation of NiO NPs and the magnitude and pattern of inflammation was similar with NiCl(2) at 24 h post-instillation. The eosinophil recruitment by NiO NPs was not related with either the levels of total IgE or anaphylatoxins. The lysis of alveolar macrophages and normal lung tissue showed high levels of intracellular eotaxin and the levels of LDH showed positive correlation with the levels of eotaxin. CONCLUSIONS: Instillation of NiO NPs produced neutrophilia at 1 and 2 days after instillation, while the mixed type of neutrophilic and eosinophilic inflammation was produced at 3 and 4 days post-instillation, which was consistent with NiCl(2). The mechanism of the eosinophilia involves the direct release of intracellular eotaxin due to the rupture of cells by the accumulated solubilized nickel ions in the phagolysosome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12989-016-0142-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-48998902016-06-10 Nickel oxide nanoparticles can recruit eosinophils in the lungs of rats by the direct release of intracellular eotaxin Lee, Seonghan Hwang, Sung-Hyun Jeong, Jiyoung Han, Youngju Kim, Sung-Hyun Lee, Dong-Keon Lee, Hae-Suk Chung, Seung-Tae Jeong, Jayoung Roh, Changhyun Huh, Yun Seok Cho, Wan-Seob Part Fibre Toxicol Research BACKGROUND: Instillation of highly soluble nanoparticles (NPs) into the lungs of rodents can cause acute eosinophilia without any previous sensitizations by the role of dissolved ions. However, whether gradually dissolving NPs can cause the same type of eosinophilia remains to be elucidated. We selected nickel oxide (NiO) as a gradually dissolving NP and evaluated the time course pulmonary inflammation pattern as well as its mechanisms. METHODS: NiO NPs were intratracheally instilled into female Wistar rats at various concentrations (50, 100, and 200 cm(2)/rat) and the lung inflammation was evaluated at various time-points (1, 2, 3, and 4 days). As positive controls, NiCl(2) and the ovalbumin-induced allergic airway inflammation model was applied. NiCl(2) was instilled at 171.1 μg Ni/rat, which is equivalent nickel concentration of 200 cm(2)/rat of NiO NPs. Cytological analysis and biochemical analysis including lactate dehydrogenase (LDH), total protein, and pro-inflammatory cytokines were measured in bronchoalveolar lavage fluid (BALF). The levels of total immunoglobulin E (IgE) and anaphylatoxins (C3a and C5a) were measured in BALF and serum. The levels of eotaxin were measured in the alveolar macrophages and normal lung tissue before and after addition of cell lysis buffer to evaluate whether the direct lysis of cells can release intracellular eotaxin. RESULTS: NiO NPs produced acute neutrophilic inflammation throughout the study. However, eosinophils were recruited at 3 and 4 days post-instillation of NiO NPs and the magnitude and pattern of inflammation was similar with NiCl(2) at 24 h post-instillation. The eosinophil recruitment by NiO NPs was not related with either the levels of total IgE or anaphylatoxins. The lysis of alveolar macrophages and normal lung tissue showed high levels of intracellular eotaxin and the levels of LDH showed positive correlation with the levels of eotaxin. CONCLUSIONS: Instillation of NiO NPs produced neutrophilia at 1 and 2 days after instillation, while the mixed type of neutrophilic and eosinophilic inflammation was produced at 3 and 4 days post-instillation, which was consistent with NiCl(2). The mechanism of the eosinophilia involves the direct release of intracellular eotaxin due to the rupture of cells by the accumulated solubilized nickel ions in the phagolysosome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12989-016-0142-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-09 /pmc/articles/PMC4899890/ /pubmed/27283431 http://dx.doi.org/10.1186/s12989-016-0142-8 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Lee, Seonghan
Hwang, Sung-Hyun
Jeong, Jiyoung
Han, Youngju
Kim, Sung-Hyun
Lee, Dong-Keon
Lee, Hae-Suk
Chung, Seung-Tae
Jeong, Jayoung
Roh, Changhyun
Huh, Yun Seok
Cho, Wan-Seob
Nickel oxide nanoparticles can recruit eosinophils in the lungs of rats by the direct release of intracellular eotaxin
title Nickel oxide nanoparticles can recruit eosinophils in the lungs of rats by the direct release of intracellular eotaxin
title_full Nickel oxide nanoparticles can recruit eosinophils in the lungs of rats by the direct release of intracellular eotaxin
title_fullStr Nickel oxide nanoparticles can recruit eosinophils in the lungs of rats by the direct release of intracellular eotaxin
title_full_unstemmed Nickel oxide nanoparticles can recruit eosinophils in the lungs of rats by the direct release of intracellular eotaxin
title_short Nickel oxide nanoparticles can recruit eosinophils in the lungs of rats by the direct release of intracellular eotaxin
title_sort nickel oxide nanoparticles can recruit eosinophils in the lungs of rats by the direct release of intracellular eotaxin
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899890/
https://www.ncbi.nlm.nih.gov/pubmed/27283431
http://dx.doi.org/10.1186/s12989-016-0142-8
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