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The Effects of Silica Nanoparticles in Macrophage Cells

Silica nanoparticles, which are applicable in many industrial fields, have been reported to induce cellular changes such as cytotoxicity in various cells and fibrosis in lungs. Because the immune system is the primary targeting organ reacting to internalized exogenous nanoparticles, we tried to figu...

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Autores principales: Kim, Seungjae, Jang, Jiyoung, Kim, Hyojin, Choi, Hoon, Lee, Kangtaek, Choi, In-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566426/
https://www.ncbi.nlm.nih.gov/pubmed/23397001
http://dx.doi.org/10.4110/in.2012.12.6.296
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author Kim, Seungjae
Jang, Jiyoung
Kim, Hyojin
Choi, Hoon
Lee, Kangtaek
Choi, In-Hong
author_facet Kim, Seungjae
Jang, Jiyoung
Kim, Hyojin
Choi, Hoon
Lee, Kangtaek
Choi, In-Hong
author_sort Kim, Seungjae
collection PubMed
description Silica nanoparticles, which are applicable in many industrial fields, have been reported to induce cellular changes such as cytotoxicity in various cells and fibrosis in lungs. Because the immune system is the primary targeting organ reacting to internalized exogenous nanoparticles, we tried to figure out the immunostimulatory effect of silica nanoparticles in macrophages using differently sized silica nanoparticles. Using U937 cells we assessed cytotoxicity by CCK-8 assay, ROS generation by CM-H(2)DCFDA, intracellular Ca(++) levels by staining with Fluo4-AM and IL-8 production by ELISA. At non-toxic concentration, the intracellular Ca(++) level has increased immediately after exposure to 15 nm particles, not to larger particles. ROS generation was detected significantly in response to 15 nm particles. However, all three different sizes of silica nanoparticles induced IL-8 production. 15 nm silica nanoparticles are more stimulatory than larger particles in cytotoxicity, intracellular Ca(++) increase and ROS generation. But IL-8 production was induced to same levels with 50 or 100 nm particles. Therefore, IL-8 production induced by silica nanoparticles may be dependent on other mechanisms rather than intracellular Ca(++) increase and ROS generation.
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spelling pubmed-35664262013-02-08 The Effects of Silica Nanoparticles in Macrophage Cells Kim, Seungjae Jang, Jiyoung Kim, Hyojin Choi, Hoon Lee, Kangtaek Choi, In-Hong Immune Netw Brief Communication Silica nanoparticles, which are applicable in many industrial fields, have been reported to induce cellular changes such as cytotoxicity in various cells and fibrosis in lungs. Because the immune system is the primary targeting organ reacting to internalized exogenous nanoparticles, we tried to figure out the immunostimulatory effect of silica nanoparticles in macrophages using differently sized silica nanoparticles. Using U937 cells we assessed cytotoxicity by CCK-8 assay, ROS generation by CM-H(2)DCFDA, intracellular Ca(++) levels by staining with Fluo4-AM and IL-8 production by ELISA. At non-toxic concentration, the intracellular Ca(++) level has increased immediately after exposure to 15 nm particles, not to larger particles. ROS generation was detected significantly in response to 15 nm particles. However, all three different sizes of silica nanoparticles induced IL-8 production. 15 nm silica nanoparticles are more stimulatory than larger particles in cytotoxicity, intracellular Ca(++) increase and ROS generation. But IL-8 production was induced to same levels with 50 or 100 nm particles. Therefore, IL-8 production induced by silica nanoparticles may be dependent on other mechanisms rather than intracellular Ca(++) increase and ROS generation. The Korean Association of Immunologists 2012-12 2012-12-31 /pmc/articles/PMC3566426/ /pubmed/23397001 http://dx.doi.org/10.4110/in.2012.12.6.296 Text en Copyright © 2012 The Korean Association of Immunologists http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communication
Kim, Seungjae
Jang, Jiyoung
Kim, Hyojin
Choi, Hoon
Lee, Kangtaek
Choi, In-Hong
The Effects of Silica Nanoparticles in Macrophage Cells
title The Effects of Silica Nanoparticles in Macrophage Cells
title_full The Effects of Silica Nanoparticles in Macrophage Cells
title_fullStr The Effects of Silica Nanoparticles in Macrophage Cells
title_full_unstemmed The Effects of Silica Nanoparticles in Macrophage Cells
title_short The Effects of Silica Nanoparticles in Macrophage Cells
title_sort effects of silica nanoparticles in macrophage cells
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566426/
https://www.ncbi.nlm.nih.gov/pubmed/23397001
http://dx.doi.org/10.4110/in.2012.12.6.296
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