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Systemic Immune Effects of Titanium Dioxide Nanoparticles after Repeated Intratracheal Instillation in Rat
The potential immune effects of titanium dioxide nanoparticles (nano-TiO(2)) are raising concern. Our previous study verified that nano-TiO(2) induce local immune response in lung tissue followed by intratracheal instillation administration. In this study, we aim to evaluate the systemic immune effe...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013672/ https://www.ncbi.nlm.nih.gov/pubmed/24758935 http://dx.doi.org/10.3390/ijms15046961 |
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author | Fu, Yanyun Zhang, Yanqiu Chang, Xuhong Zhang, Yingjian Ma, Shumei Sui, Jing Yin, Lihong Pu, Yuepu Liang, Geyu |
author_facet | Fu, Yanyun Zhang, Yanqiu Chang, Xuhong Zhang, Yingjian Ma, Shumei Sui, Jing Yin, Lihong Pu, Yuepu Liang, Geyu |
author_sort | Fu, Yanyun |
collection | PubMed |
description | The potential immune effects of titanium dioxide nanoparticles (nano-TiO(2)) are raising concern. Our previous study verified that nano-TiO(2) induce local immune response in lung tissue followed by intratracheal instillation administration. In this study, we aim to evaluate the systemic immune effects of nano-TiO(2). Sprague Dawley rats were treated by intratracheal instillation with nano-TiO(2) at doses of 0.5, 4, and 32 mg/kg body weight, micro-TiO(2) with 32 mg/kg body weight and 0.9% NaCl, respectively. The exposure was conducted twice a week, for four consecutive weeks. Histopathological immune organs from exposed animals showed slight congestion in spleen, generally brown particulate deposition in cervical and axillary lymph node. Furthermore, immune function response was characterized by increased proliferation of T cells and B cells following mitogen stimulation and enhanced natural killer (NK) cell killing activity in spleen, accompanying by increased number of B cells in blood. No significant changes of Th1-type cytokines (IL-2 and INF-γ) and Th2-type cytokines (TNF-α and IL-6) were observed. Intratracheal exposure to nano-TiO(2) may be one of triggers to be responsible for the systemic immune response. Further study is needed to confirm long-lasting lymphocyte responses and the potential mechanisms. |
format | Online Article Text |
id | pubmed-4013672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-40136722014-05-08 Systemic Immune Effects of Titanium Dioxide Nanoparticles after Repeated Intratracheal Instillation in Rat Fu, Yanyun Zhang, Yanqiu Chang, Xuhong Zhang, Yingjian Ma, Shumei Sui, Jing Yin, Lihong Pu, Yuepu Liang, Geyu Int J Mol Sci Article The potential immune effects of titanium dioxide nanoparticles (nano-TiO(2)) are raising concern. Our previous study verified that nano-TiO(2) induce local immune response in lung tissue followed by intratracheal instillation administration. In this study, we aim to evaluate the systemic immune effects of nano-TiO(2). Sprague Dawley rats were treated by intratracheal instillation with nano-TiO(2) at doses of 0.5, 4, and 32 mg/kg body weight, micro-TiO(2) with 32 mg/kg body weight and 0.9% NaCl, respectively. The exposure was conducted twice a week, for four consecutive weeks. Histopathological immune organs from exposed animals showed slight congestion in spleen, generally brown particulate deposition in cervical and axillary lymph node. Furthermore, immune function response was characterized by increased proliferation of T cells and B cells following mitogen stimulation and enhanced natural killer (NK) cell killing activity in spleen, accompanying by increased number of B cells in blood. No significant changes of Th1-type cytokines (IL-2 and INF-γ) and Th2-type cytokines (TNF-α and IL-6) were observed. Intratracheal exposure to nano-TiO(2) may be one of triggers to be responsible for the systemic immune response. Further study is needed to confirm long-lasting lymphocyte responses and the potential mechanisms. Molecular Diversity Preservation International (MDPI) 2014-04-22 /pmc/articles/PMC4013672/ /pubmed/24758935 http://dx.doi.org/10.3390/ijms15046961 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Fu, Yanyun Zhang, Yanqiu Chang, Xuhong Zhang, Yingjian Ma, Shumei Sui, Jing Yin, Lihong Pu, Yuepu Liang, Geyu Systemic Immune Effects of Titanium Dioxide Nanoparticles after Repeated Intratracheal Instillation in Rat |
title | Systemic Immune Effects of Titanium Dioxide Nanoparticles after Repeated Intratracheal Instillation in Rat |
title_full | Systemic Immune Effects of Titanium Dioxide Nanoparticles after Repeated Intratracheal Instillation in Rat |
title_fullStr | Systemic Immune Effects of Titanium Dioxide Nanoparticles after Repeated Intratracheal Instillation in Rat |
title_full_unstemmed | Systemic Immune Effects of Titanium Dioxide Nanoparticles after Repeated Intratracheal Instillation in Rat |
title_short | Systemic Immune Effects of Titanium Dioxide Nanoparticles after Repeated Intratracheal Instillation in Rat |
title_sort | systemic immune effects of titanium dioxide nanoparticles after repeated intratracheal instillation in rat |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013672/ https://www.ncbi.nlm.nih.gov/pubmed/24758935 http://dx.doi.org/10.3390/ijms15046961 |
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