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Gold nanoparticles disrupt actin organization and pulmonary endothelial barriers
This study explored the impact of gold nanoparticles on the metabolic activity and morphology of human pulmonary endothelial cell monolayers. We developed a gold nanoparticle library of three different sizes and two surface chemistries that include anionic citrate and the cationic polyelectrolyte po...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414109/ https://www.ncbi.nlm.nih.gov/pubmed/32770112 http://dx.doi.org/10.1038/s41598-020-70148-1 |
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author | Sinclair, Whitney E. Chang, Huei-Huei Dan, Arkaprava Kenis, Paul J. A. Murphy, Catherine J. Leckband, Deborah E. |
author_facet | Sinclair, Whitney E. Chang, Huei-Huei Dan, Arkaprava Kenis, Paul J. A. Murphy, Catherine J. Leckband, Deborah E. |
author_sort | Sinclair, Whitney E. |
collection | PubMed |
description | This study explored the impact of gold nanoparticles on the metabolic activity and morphology of human pulmonary endothelial cell monolayers. We developed a gold nanoparticle library of three different sizes and two surface chemistries that include anionic citrate and the cationic polyelectrolyte poly(allylamine hydrochloride). The nanoparticles were characterized in cell culture medium to assess how their physical properties are altered after exposure to biological fluids. A bovine serum albumin pretreatment protocol was developed to stabilize the nanoparticles in cell culture medium. Results of this study show that an 18 h exposure of human pulmonary artery endothelial cells to the different nanoparticles modestly affects cellular metabolic activity. However, nanoparticle exposure perturbs the cortical actin networks and induces the formation of intercellular gaps. In particular, exposure to the poly(allylamine hydrochloride)-coated particles reduces the area of cell–cell junctions—a change that correlates with increased leakiness of endothelial barriers. The presence of excess polyelectrolyte capping agents in the supernatant of poly(allylamine hydrochloride)-coated nanoparticles significantly impacts endothelial morphology. Pretreatment of the particle supernatant with bovine serum albumin mitigates the negative effects of free or bound polyelectrolytes on endothelial cell monolayers. |
format | Online Article Text |
id | pubmed-7414109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74141092020-08-10 Gold nanoparticles disrupt actin organization and pulmonary endothelial barriers Sinclair, Whitney E. Chang, Huei-Huei Dan, Arkaprava Kenis, Paul J. A. Murphy, Catherine J. Leckband, Deborah E. Sci Rep Article This study explored the impact of gold nanoparticles on the metabolic activity and morphology of human pulmonary endothelial cell monolayers. We developed a gold nanoparticle library of three different sizes and two surface chemistries that include anionic citrate and the cationic polyelectrolyte poly(allylamine hydrochloride). The nanoparticles were characterized in cell culture medium to assess how their physical properties are altered after exposure to biological fluids. A bovine serum albumin pretreatment protocol was developed to stabilize the nanoparticles in cell culture medium. Results of this study show that an 18 h exposure of human pulmonary artery endothelial cells to the different nanoparticles modestly affects cellular metabolic activity. However, nanoparticle exposure perturbs the cortical actin networks and induces the formation of intercellular gaps. In particular, exposure to the poly(allylamine hydrochloride)-coated particles reduces the area of cell–cell junctions—a change that correlates with increased leakiness of endothelial barriers. The presence of excess polyelectrolyte capping agents in the supernatant of poly(allylamine hydrochloride)-coated nanoparticles significantly impacts endothelial morphology. Pretreatment of the particle supernatant with bovine serum albumin mitigates the negative effects of free or bound polyelectrolytes on endothelial cell monolayers. Nature Publishing Group UK 2020-08-07 /pmc/articles/PMC7414109/ /pubmed/32770112 http://dx.doi.org/10.1038/s41598-020-70148-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sinclair, Whitney E. Chang, Huei-Huei Dan, Arkaprava Kenis, Paul J. A. Murphy, Catherine J. Leckband, Deborah E. Gold nanoparticles disrupt actin organization and pulmonary endothelial barriers |
title | Gold nanoparticles disrupt actin organization and pulmonary endothelial barriers |
title_full | Gold nanoparticles disrupt actin organization and pulmonary endothelial barriers |
title_fullStr | Gold nanoparticles disrupt actin organization and pulmonary endothelial barriers |
title_full_unstemmed | Gold nanoparticles disrupt actin organization and pulmonary endothelial barriers |
title_short | Gold nanoparticles disrupt actin organization and pulmonary endothelial barriers |
title_sort | gold nanoparticles disrupt actin organization and pulmonary endothelial barriers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414109/ https://www.ncbi.nlm.nih.gov/pubmed/32770112 http://dx.doi.org/10.1038/s41598-020-70148-1 |
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