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Immunomodulatory properties of titanium dioxide nanostructural materials
OBJECTIVES: Although titanium dioxide (TiO(2)) nanostructural materials have been widely used in Biology and Medicine, very little is known about immunomodulation mechanism of these materials. Objectives of this study are to investigate in vitro immunomodulatory effects of TiO(2). Immunosuppressant...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892028/ https://www.ncbi.nlm.nih.gov/pubmed/29674801 http://dx.doi.org/10.4103/ijp.IJP_536_16 |
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author | Latha, T. Sree Reddy, Madhava C. R. Durbaka, Prasad V. Muthukonda, Shankar V. Lomada, Dakshayani |
author_facet | Latha, T. Sree Reddy, Madhava C. R. Durbaka, Prasad V. Muthukonda, Shankar V. Lomada, Dakshayani |
author_sort | Latha, T. Sree |
collection | PubMed |
description | OBJECTIVES: Although titanium dioxide (TiO(2)) nanostructural materials have been widely used in Biology and Medicine, very little is known about immunomodulation mechanism of these materials. Objectives of this study are to investigate in vitro immunomodulatory effects of TiO(2). Immunosuppressant may lower immune responses and are helpful for the treatment of graft versus host diseases and autoimmune disorders. MATERIALS AND METHODS: In this study, we used H(2)Ti(3)O(7) titanium dioxide nanotubes (TNT) nanotubes along with commercial TiO(2) nanoparticles (TNP) and TiO(2) fine particles (TFP). We investigated the in vitro immunomodulatory effects of TNP, TNT, and TFP using mixed lymphocyte reaction (MLR). Suppression was studied by 3-(4, 5-dimethylthiazol-2yl)-2, 5-diphenyl tetrazolium bromide (MTT) assay. Cytokine profile was measured by enzyme-linked immunosorbent assay (ELISA). RESULTS AND CONCLUSIONS: The results from this study illustrated that the TiO(2) nanostructural materials strongly suppressed splenocytes proliferation in MLR. For TNP and TNT, at 50 μg/ml suppression of 20%–25% and 30%–35%, respectively, and for TFP at 100 μg/ml suppression was 25%–30% was observed. Suppression of splenocytes proliferation in the presence of TNP, TNT, and TFP demonstrated that these nanostructural materials probably block T-cell-mediated responses in vitro. Our ELISA results confirmed that significantly lower levels of Th1 type cytokines (interleukin-2, interferon-γ) in the 48 h MLR culture supernatants. Our data suggest that TiO(2) nanostructural materials suppress splenocytes proliferation by suppressing Th1 cytokines. |
format | Online Article Text |
id | pubmed-5892028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58920282018-04-19 Immunomodulatory properties of titanium dioxide nanostructural materials Latha, T. Sree Reddy, Madhava C. R. Durbaka, Prasad V. Muthukonda, Shankar V. Lomada, Dakshayani Indian J Pharmacol Research Article OBJECTIVES: Although titanium dioxide (TiO(2)) nanostructural materials have been widely used in Biology and Medicine, very little is known about immunomodulation mechanism of these materials. Objectives of this study are to investigate in vitro immunomodulatory effects of TiO(2). Immunosuppressant may lower immune responses and are helpful for the treatment of graft versus host diseases and autoimmune disorders. MATERIALS AND METHODS: In this study, we used H(2)Ti(3)O(7) titanium dioxide nanotubes (TNT) nanotubes along with commercial TiO(2) nanoparticles (TNP) and TiO(2) fine particles (TFP). We investigated the in vitro immunomodulatory effects of TNP, TNT, and TFP using mixed lymphocyte reaction (MLR). Suppression was studied by 3-(4, 5-dimethylthiazol-2yl)-2, 5-diphenyl tetrazolium bromide (MTT) assay. Cytokine profile was measured by enzyme-linked immunosorbent assay (ELISA). RESULTS AND CONCLUSIONS: The results from this study illustrated that the TiO(2) nanostructural materials strongly suppressed splenocytes proliferation in MLR. For TNP and TNT, at 50 μg/ml suppression of 20%–25% and 30%–35%, respectively, and for TFP at 100 μg/ml suppression was 25%–30% was observed. Suppression of splenocytes proliferation in the presence of TNP, TNT, and TFP demonstrated that these nanostructural materials probably block T-cell-mediated responses in vitro. Our ELISA results confirmed that significantly lower levels of Th1 type cytokines (interleukin-2, interferon-γ) in the 48 h MLR culture supernatants. Our data suggest that TiO(2) nanostructural materials suppress splenocytes proliferation by suppressing Th1 cytokines. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5892028/ /pubmed/29674801 http://dx.doi.org/10.4103/ijp.IJP_536_16 Text en Copyright: © 2018 Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Latha, T. Sree Reddy, Madhava C. R. Durbaka, Prasad V. Muthukonda, Shankar V. Lomada, Dakshayani Immunomodulatory properties of titanium dioxide nanostructural materials |
title | Immunomodulatory properties of titanium dioxide nanostructural materials |
title_full | Immunomodulatory properties of titanium dioxide nanostructural materials |
title_fullStr | Immunomodulatory properties of titanium dioxide nanostructural materials |
title_full_unstemmed | Immunomodulatory properties of titanium dioxide nanostructural materials |
title_short | Immunomodulatory properties of titanium dioxide nanostructural materials |
title_sort | immunomodulatory properties of titanium dioxide nanostructural materials |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892028/ https://www.ncbi.nlm.nih.gov/pubmed/29674801 http://dx.doi.org/10.4103/ijp.IJP_536_16 |
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