Multi-walled carbon nanotube induced frustrated phagocytosis, cytotoxicity and pro-inflammatory conditions in macrophages are length dependent and greater than that of asbestos

•MWCNTs were synthesised with specific physicochemical characteristics.•Particle characteristics known to induce respiratory disease were assessed: length, iron content, crystallinity.•MWCNT length was found to be a driving force in biological responses.•Iron and crystal structure had less influence...

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Veröffentlicht in:Toxicology in vitro 2015-10, Vol.29 (7), p.1513-1528
Hauptverfasser: Boyles, Matthew S.P., Young, Lesley, Brown, David M., MacCalman, Laura, Cowie, Hilary, Moisala, Anna, Smail, Fiona, Smith, Paula J.W., Proudfoot, Lorna, Windle, Alan H., Stone, Vicki
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container_end_page 1528
container_issue 7
container_start_page 1513
container_title Toxicology in vitro
container_volume 29
creator Boyles, Matthew S.P.
Young, Lesley
Brown, David M.
MacCalman, Laura
Cowie, Hilary
Moisala, Anna
Smail, Fiona
Smith, Paula J.W.
Proudfoot, Lorna
Windle, Alan H.
Stone, Vicki
description •MWCNTs were synthesised with specific physicochemical characteristics.•Particle characteristics known to induce respiratory disease were assessed: length, iron content, crystallinity.•MWCNT length was found to be a driving force in biological responses.•Iron and crystal structure had less influence in biological responses.•MWCNTs induced greater detrimental biological responses compared to asbestos. The potential toxicity of carbon nanotubes (CNTs) has been compared to pathogenic fibres such as asbestos. It is important to test this hypothesis to ascertain safe methods for CNT production, handling and disposal. In this study aspects reported to contribute to CNT toxicity were assessed: length, aspect ratio, iron content and crystallinity; with responses compared to industrially produced MWCNTs and toxicologically relevant materials such as asbestos. The impacts of these particles on a range of macrophage models in vitro were assessed due to the key role of macrophages in particle clearance and particle/fibre-induced disease. Industrially produced and long MWCNTs were cytotoxic to cells, and were potent in inducing pro-inflammatory and pro-fibrotic immune responses. Short CNTs did not induce any cytotoxicity. Frustrated phagocytosis was most evident in response to long CNTs, as was respiratory burst and reduction in phagocytic ability. Short CNTs, metal content and crystallinity had less or no influence on these endpoints, suggesting that many responses were fibre-length dependent. This study demonstrates that CNTs are potentially pathogenic, as they were routinely found to induce detrimental responses in macrophages greater than those induced by asbestos at the same mass-based dose.
doi_str_mv 10.1016/j.tiv.2015.06.012
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The potential toxicity of carbon nanotubes (CNTs) has been compared to pathogenic fibres such as asbestos. It is important to test this hypothesis to ascertain safe methods for CNT production, handling and disposal. In this study aspects reported to contribute to CNT toxicity were assessed: length, aspect ratio, iron content and crystallinity; with responses compared to industrially produced MWCNTs and toxicologically relevant materials such as asbestos. The impacts of these particles on a range of macrophage models in vitro were assessed due to the key role of macrophages in particle clearance and particle/fibre-induced disease. Industrially produced and long MWCNTs were cytotoxic to cells, and were potent in inducing pro-inflammatory and pro-fibrotic immune responses. Short CNTs did not induce any cytotoxicity. Frustrated phagocytosis was most evident in response to long CNTs, as was respiratory burst and reduction in phagocytic ability. Short CNTs, metal content and crystallinity had less or no influence on these endpoints, suggesting that many responses were fibre-length dependent. 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The potential toxicity of carbon nanotubes (CNTs) has been compared to pathogenic fibres such as asbestos. It is important to test this hypothesis to ascertain safe methods for CNT production, handling and disposal. In this study aspects reported to contribute to CNT toxicity were assessed: length, aspect ratio, iron content and crystallinity; with responses compared to industrially produced MWCNTs and toxicologically relevant materials such as asbestos. The impacts of these particles on a range of macrophage models in vitro were assessed due to the key role of macrophages in particle clearance and particle/fibre-induced disease. Industrially produced and long MWCNTs were cytotoxic to cells, and were potent in inducing pro-inflammatory and pro-fibrotic immune responses. Short CNTs did not induce any cytotoxicity. Frustrated phagocytosis was most evident in response to long CNTs, as was respiratory burst and reduction in phagocytic ability. Short CNTs, metal content and crystallinity had less or no influence on these endpoints, suggesting that many responses were fibre-length dependent. This study demonstrates that CNTs are potentially pathogenic, as they were routinely found to induce detrimental responses in macrophages greater than those induced by asbestos at the same mass-based dose.</description><subject>Animals</subject><subject>Asbestos</subject><subject>Asbestos, Amosite - toxicity</subject><subject>Bronchoalveolar Lavage Fluid - cytology</subject><subject>Carbon nanotubes</subject><subject>Cell Line</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>Chemokine CCL2 - metabolism</subject><subject>Frustrated phagocytosis</subject><subject>Humans</subject><subject>Iron - analysis</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - physiology</subject><subject>Male</subject><subject>Mice</subject><subject>Nanoparticles</subject><subject>Nanotubes, Carbon - chemistry</subject><subject>Nanotubes, Carbon - toxicity</subject><subject>Particle Size</subject><subject>Phagocytosis - drug effects</subject><subject>Rats, Sprague-Dawley</subject><subject>Soot - toxicity</subject><subject>Transforming Growth Factor beta1 - metabolism</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0887-2333</issn><issn>1879-3177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc2OFCEUhYnROO3oA7gxLF1YJT9VFBVXZuJfMsaNrgkFl246VdACNdpv5SNK2aNLN3AD556Tkw-h55S0lFDx-tgWf9cyQvuWiJZQ9gDtqBzGhtNheIh2RMqhYZzzK_Qk5yMhpJeMPEZXTBApKOM79OvzOhff_NDzDBYbnaYYcNAhlnUC7INdTX13ac0l6VLH00HvozmXmH1-hbehxJ_e-HLGOtTvFBsf3KyXRZeYztjEYH3xMeTqhhdtUtwsIGOdAM8Q9uWALZwgWAjlj8c-QY1KuBx02I6Co8M6T5Br6lP0yOk5w7P7-xp9e__u683H5vbLh083b28b0_GuNNxKKoENowNHmRYdCNG5TjCQTkwjtZ2bBib7viNdP3AygBsZjMBcXRPW8Gv08uJbG31fa7RafDYwzzpAXLOiA2W94L0kVUov0tot5wROnZJfdDorStQGSh1VBaU2UIoIVUHVnRf39uu0gP238ZdMFby5CKCWvPOQVDYeQqXhE5iibPT_sf8NEyGo8A</recordid><startdate>201510</startdate><enddate>201510</enddate><creator>Boyles, Matthew S.P.</creator><creator>Young, Lesley</creator><creator>Brown, David M.</creator><creator>MacCalman, Laura</creator><creator>Cowie, Hilary</creator><creator>Moisala, Anna</creator><creator>Smail, Fiona</creator><creator>Smith, Paula J.W.</creator><creator>Proudfoot, Lorna</creator><creator>Windle, Alan H.</creator><creator>Stone, Vicki</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope></search><sort><creationdate>201510</creationdate><title>Multi-walled carbon nanotube induced frustrated phagocytosis, cytotoxicity and pro-inflammatory conditions in macrophages are length dependent and greater than that of asbestos</title><author>Boyles, Matthew S.P. ; 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The potential toxicity of carbon nanotubes (CNTs) has been compared to pathogenic fibres such as asbestos. It is important to test this hypothesis to ascertain safe methods for CNT production, handling and disposal. In this study aspects reported to contribute to CNT toxicity were assessed: length, aspect ratio, iron content and crystallinity; with responses compared to industrially produced MWCNTs and toxicologically relevant materials such as asbestos. The impacts of these particles on a range of macrophage models in vitro were assessed due to the key role of macrophages in particle clearance and particle/fibre-induced disease. Industrially produced and long MWCNTs were cytotoxic to cells, and were potent in inducing pro-inflammatory and pro-fibrotic immune responses. Short CNTs did not induce any cytotoxicity. Frustrated phagocytosis was most evident in response to long CNTs, as was respiratory burst and reduction in phagocytic ability. Short CNTs, metal content and crystallinity had less or no influence on these endpoints, suggesting that many responses were fibre-length dependent. This study demonstrates that CNTs are potentially pathogenic, as they were routinely found to induce detrimental responses in macrophages greater than those induced by asbestos at the same mass-based dose.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>26086123</pmid><doi>10.1016/j.tiv.2015.06.012</doi><tpages>16</tpages></addata></record>
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subjects Animals
Asbestos
Asbestos, Amosite - toxicity
Bronchoalveolar Lavage Fluid - cytology
Carbon nanotubes
Cell Line
Cell Survival - drug effects
Cells, Cultured
Chemokine CCL2 - metabolism
Frustrated phagocytosis
Humans
Iron - analysis
Macrophages - drug effects
Macrophages - metabolism
Macrophages - physiology
Male
Mice
Nanoparticles
Nanotubes, Carbon - chemistry
Nanotubes, Carbon - toxicity
Particle Size
Phagocytosis - drug effects
Rats, Sprague-Dawley
Soot - toxicity
Transforming Growth Factor beta1 - metabolism
Tumor Necrosis Factor-alpha - metabolism
title Multi-walled carbon nanotube induced frustrated phagocytosis, cytotoxicity and pro-inflammatory conditions in macrophages are length dependent and greater than that of asbestos
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