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Cellular Responses of Industrially Relevant Silica Dust on Human Glial Cells In Vitro

Despite the rigorous emission control measures in the ferroalloy industry, there are still emissions of dust during the production of various alloys. Dust particles were collected from laboratory scale processes where oxide particulate matter was formed from liquid silicon (metallurgical grade). The...

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Autores principales: Arnoldussen, Yke Jildouw, Kringlen Ervik, Torunn, Baarnes Eriksen, Mina, Kero, Ida, Skaug, Vidar, Zienolddiny, Shanbeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359019/
https://www.ncbi.nlm.nih.gov/pubmed/30654492
http://dx.doi.org/10.3390/ijms20020358
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author Arnoldussen, Yke Jildouw
Kringlen Ervik, Torunn
Baarnes Eriksen, Mina
Kero, Ida
Skaug, Vidar
Zienolddiny, Shanbeh
author_facet Arnoldussen, Yke Jildouw
Kringlen Ervik, Torunn
Baarnes Eriksen, Mina
Kero, Ida
Skaug, Vidar
Zienolddiny, Shanbeh
author_sort Arnoldussen, Yke Jildouw
collection PubMed
description Despite the rigorous emission control measures in the ferroalloy industry, there are still emissions of dust during the production of various alloys. Dust particles were collected from laboratory scale processes where oxide particulate matter was formed from liquid silicon (metallurgical grade). The dust was produced in a dry air atmosphere to mimic industrial conditions. To investigate possible effects of ultrafine dust on the central nervous system, a human astrocytic cell line was employed to investigate inflammatory effects of particles as astrocytes play a number of active and neuron supporting roles in the brain. Toxicity on the astrocytes by amorphous silica generated in laboratory scale was compared to crystalline macro-sized silica using several doses to determine toxicological dose response curves. The cell viability experiments indicated that low particle doses of amorphous silica induced a small nonsignificant reduction in cell viability compared to crystalline silica which led to increased levels of toxicity. The gene expression of amyloid precursor protein (APP), a biomarker of neurodegenerative disease, was affected by particle exposure. Furthermore, particle exposure, in a dose-and time-dependent manner, affected the ability of the cells to communicate through gap junction channels. In conclusion, in vitro studies using low doses of particles are important to understand mechanisms of toxicity of occupational exposure to silica particles. However, these studies cannot be extrapolated to real exposure scenarios at work place, therefore, controlling and keeping the particle exposure levels low at the work place, would prevent potential negative health effects.
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spelling pubmed-63590192019-02-06 Cellular Responses of Industrially Relevant Silica Dust on Human Glial Cells In Vitro Arnoldussen, Yke Jildouw Kringlen Ervik, Torunn Baarnes Eriksen, Mina Kero, Ida Skaug, Vidar Zienolddiny, Shanbeh Int J Mol Sci Article Despite the rigorous emission control measures in the ferroalloy industry, there are still emissions of dust during the production of various alloys. Dust particles were collected from laboratory scale processes where oxide particulate matter was formed from liquid silicon (metallurgical grade). The dust was produced in a dry air atmosphere to mimic industrial conditions. To investigate possible effects of ultrafine dust on the central nervous system, a human astrocytic cell line was employed to investigate inflammatory effects of particles as astrocytes play a number of active and neuron supporting roles in the brain. Toxicity on the astrocytes by amorphous silica generated in laboratory scale was compared to crystalline macro-sized silica using several doses to determine toxicological dose response curves. The cell viability experiments indicated that low particle doses of amorphous silica induced a small nonsignificant reduction in cell viability compared to crystalline silica which led to increased levels of toxicity. The gene expression of amyloid precursor protein (APP), a biomarker of neurodegenerative disease, was affected by particle exposure. Furthermore, particle exposure, in a dose-and time-dependent manner, affected the ability of the cells to communicate through gap junction channels. In conclusion, in vitro studies using low doses of particles are important to understand mechanisms of toxicity of occupational exposure to silica particles. However, these studies cannot be extrapolated to real exposure scenarios at work place, therefore, controlling and keeping the particle exposure levels low at the work place, would prevent potential negative health effects. MDPI 2019-01-16 /pmc/articles/PMC6359019/ /pubmed/30654492 http://dx.doi.org/10.3390/ijms20020358 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Arnoldussen, Yke Jildouw
Kringlen Ervik, Torunn
Baarnes Eriksen, Mina
Kero, Ida
Skaug, Vidar
Zienolddiny, Shanbeh
Cellular Responses of Industrially Relevant Silica Dust on Human Glial Cells In Vitro
title Cellular Responses of Industrially Relevant Silica Dust on Human Glial Cells In Vitro
title_full Cellular Responses of Industrially Relevant Silica Dust on Human Glial Cells In Vitro
title_fullStr Cellular Responses of Industrially Relevant Silica Dust on Human Glial Cells In Vitro
title_full_unstemmed Cellular Responses of Industrially Relevant Silica Dust on Human Glial Cells In Vitro
title_short Cellular Responses of Industrially Relevant Silica Dust on Human Glial Cells In Vitro
title_sort cellular responses of industrially relevant silica dust on human glial cells in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359019/
https://www.ncbi.nlm.nih.gov/pubmed/30654492
http://dx.doi.org/10.3390/ijms20020358
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