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Cellular Responses of Human Lymphatic Endothelial Cells to Carbon Nanomaterials
One of the greatest challenges to overcome in the pursuit of the medical application of carbon nanomaterials (CNMs) is safety. Particularly, when considering the use of CNMs in drug delivery systems (DDSs), evaluation of safety at the accumulation site is an essential step. In this study, we evaluat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407296/ https://www.ncbi.nlm.nih.gov/pubmed/32674394 http://dx.doi.org/10.3390/nano10071374 |
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author | Sano, Mahoko Izumiya, Makoto Haniu, Hisao Ueda, Katsuya Konishi, Kosuke Ishida, Haruka Kuroda, Chika Uemura, Takeshi Aoki, Kaoru Matsuda, Yoshikazu Saito, Naoto |
author_facet | Sano, Mahoko Izumiya, Makoto Haniu, Hisao Ueda, Katsuya Konishi, Kosuke Ishida, Haruka Kuroda, Chika Uemura, Takeshi Aoki, Kaoru Matsuda, Yoshikazu Saito, Naoto |
author_sort | Sano, Mahoko |
collection | PubMed |
description | One of the greatest challenges to overcome in the pursuit of the medical application of carbon nanomaterials (CNMs) is safety. Particularly, when considering the use of CNMs in drug delivery systems (DDSs), evaluation of safety at the accumulation site is an essential step. In this study, we evaluated the toxicity of carbon nanohorns (CNHs), which are potential DDSs, using human lymph node endothelial cells that have been reported to accumulate CNMs, as a comparison to fibrous, multi-walled carbon nanotubes (MWCNTs) and particulate carbon black (CB). The effect of different surface characteristics was also evaluated using two types of CNHs (untreated and oxidized). In the fibrous MWCNT, cell growth suppression, as well as expression of inflammatory cytokine genes was observed, as in previous reports. In contrast, no significant toxicity was observed for particulate CB and CNHs, which was different from the report of CB cytotoxicity in vascular endothelial cells. These results show that (1) lymph endothelial cells need to be tested separately from other endothelial cells for safety evaluation of nanomaterials, and (2) the potential of CNHs as DDSs. |
format | Online Article Text |
id | pubmed-7407296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74072962020-08-11 Cellular Responses of Human Lymphatic Endothelial Cells to Carbon Nanomaterials Sano, Mahoko Izumiya, Makoto Haniu, Hisao Ueda, Katsuya Konishi, Kosuke Ishida, Haruka Kuroda, Chika Uemura, Takeshi Aoki, Kaoru Matsuda, Yoshikazu Saito, Naoto Nanomaterials (Basel) Article One of the greatest challenges to overcome in the pursuit of the medical application of carbon nanomaterials (CNMs) is safety. Particularly, when considering the use of CNMs in drug delivery systems (DDSs), evaluation of safety at the accumulation site is an essential step. In this study, we evaluated the toxicity of carbon nanohorns (CNHs), which are potential DDSs, using human lymph node endothelial cells that have been reported to accumulate CNMs, as a comparison to fibrous, multi-walled carbon nanotubes (MWCNTs) and particulate carbon black (CB). The effect of different surface characteristics was also evaluated using two types of CNHs (untreated and oxidized). In the fibrous MWCNT, cell growth suppression, as well as expression of inflammatory cytokine genes was observed, as in previous reports. In contrast, no significant toxicity was observed for particulate CB and CNHs, which was different from the report of CB cytotoxicity in vascular endothelial cells. These results show that (1) lymph endothelial cells need to be tested separately from other endothelial cells for safety evaluation of nanomaterials, and (2) the potential of CNHs as DDSs. MDPI 2020-07-14 /pmc/articles/PMC7407296/ /pubmed/32674394 http://dx.doi.org/10.3390/nano10071374 Text en © 2020 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 Sano, Mahoko Izumiya, Makoto Haniu, Hisao Ueda, Katsuya Konishi, Kosuke Ishida, Haruka Kuroda, Chika Uemura, Takeshi Aoki, Kaoru Matsuda, Yoshikazu Saito, Naoto Cellular Responses of Human Lymphatic Endothelial Cells to Carbon Nanomaterials |
title | Cellular Responses of Human Lymphatic Endothelial Cells to Carbon Nanomaterials |
title_full | Cellular Responses of Human Lymphatic Endothelial Cells to Carbon Nanomaterials |
title_fullStr | Cellular Responses of Human Lymphatic Endothelial Cells to Carbon Nanomaterials |
title_full_unstemmed | Cellular Responses of Human Lymphatic Endothelial Cells to Carbon Nanomaterials |
title_short | Cellular Responses of Human Lymphatic Endothelial Cells to Carbon Nanomaterials |
title_sort | cellular responses of human lymphatic endothelial cells to carbon nanomaterials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407296/ https://www.ncbi.nlm.nih.gov/pubmed/32674394 http://dx.doi.org/10.3390/nano10071374 |
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