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Intracellular Trafficking of Fluorescent Nanodiamonds and Regulation of Their Cellular Toxicity
[Image: see text] In this paper, cellular management of fluorescent nanodiamonds (FNDs) has been studied for better understanding in the design for potential applications of FNDs in biomedicine. The FNDs have shown to be photostable probes for bioimaging and thus are well-suited, for example, long-t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044821/ https://www.ncbi.nlm.nih.gov/pubmed/30023673 http://dx.doi.org/10.1021/acsomega.7b00339 |
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author | Prabhakar, Neeraj Khan, Meraj H. Peurla, Markus Chang, Huan-Cheng Hänninen, Pekka E. Rosenholm, Jessica M. |
author_facet | Prabhakar, Neeraj Khan, Meraj H. Peurla, Markus Chang, Huan-Cheng Hänninen, Pekka E. Rosenholm, Jessica M. |
author_sort | Prabhakar, Neeraj |
collection | PubMed |
description | [Image: see text] In this paper, cellular management of fluorescent nanodiamonds (FNDs) has been studied for better understanding in the design for potential applications of FNDs in biomedicine. The FNDs have shown to be photostable probes for bioimaging and thus are well-suited, for example, long-term tracking purposes. The FNDs also exhibit good biocompatibility and, in general, low toxicity for cell labeling. To demonstrate the underlying mechanism of cells coping the low but potentially toxic effects by nondegradable FNDs, we have studied their temporal intracellular trafficking. The FNDs were observed to be localized as distinct populations inside cells in early endosomes, lysosomes, and in proximity to the plasma membrane. The localization of FNDs in early endosomes suggests the internalization of FNDs, and lysosomal localization, in turn, can be interpreted as a prestate for exocytosis via lysosomal degradation pathway. The endocytosis and exocytosis appear to be occurring simultaneously in our observations. The mechanism of continuous endocytosis and exocytosis of FNDs could be necessary for cells to maintain normal proliferation. Furthermore, 120 h cell growth assay was performed to verify the long-term biocompatibility of FNDs for cellular studies. |
format | Online Article Text |
id | pubmed-6044821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60448212018-07-16 Intracellular Trafficking of Fluorescent Nanodiamonds and Regulation of Their Cellular Toxicity Prabhakar, Neeraj Khan, Meraj H. Peurla, Markus Chang, Huan-Cheng Hänninen, Pekka E. Rosenholm, Jessica M. ACS Omega [Image: see text] In this paper, cellular management of fluorescent nanodiamonds (FNDs) has been studied for better understanding in the design for potential applications of FNDs in biomedicine. The FNDs have shown to be photostable probes for bioimaging and thus are well-suited, for example, long-term tracking purposes. The FNDs also exhibit good biocompatibility and, in general, low toxicity for cell labeling. To demonstrate the underlying mechanism of cells coping the low but potentially toxic effects by nondegradable FNDs, we have studied their temporal intracellular trafficking. The FNDs were observed to be localized as distinct populations inside cells in early endosomes, lysosomes, and in proximity to the plasma membrane. The localization of FNDs in early endosomes suggests the internalization of FNDs, and lysosomal localization, in turn, can be interpreted as a prestate for exocytosis via lysosomal degradation pathway. The endocytosis and exocytosis appear to be occurring simultaneously in our observations. The mechanism of continuous endocytosis and exocytosis of FNDs could be necessary for cells to maintain normal proliferation. Furthermore, 120 h cell growth assay was performed to verify the long-term biocompatibility of FNDs for cellular studies. American Chemical Society 2017-06-16 /pmc/articles/PMC6044821/ /pubmed/30023673 http://dx.doi.org/10.1021/acsomega.7b00339 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Prabhakar, Neeraj Khan, Meraj H. Peurla, Markus Chang, Huan-Cheng Hänninen, Pekka E. Rosenholm, Jessica M. Intracellular Trafficking of Fluorescent Nanodiamonds and Regulation of Their Cellular Toxicity |
title | Intracellular Trafficking of Fluorescent Nanodiamonds
and Regulation of Their Cellular
Toxicity |
title_full | Intracellular Trafficking of Fluorescent Nanodiamonds
and Regulation of Their Cellular
Toxicity |
title_fullStr | Intracellular Trafficking of Fluorescent Nanodiamonds
and Regulation of Their Cellular
Toxicity |
title_full_unstemmed | Intracellular Trafficking of Fluorescent Nanodiamonds
and Regulation of Their Cellular
Toxicity |
title_short | Intracellular Trafficking of Fluorescent Nanodiamonds
and Regulation of Their Cellular
Toxicity |
title_sort | intracellular trafficking of fluorescent nanodiamonds
and regulation of their cellular
toxicity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044821/ https://www.ncbi.nlm.nih.gov/pubmed/30023673 http://dx.doi.org/10.1021/acsomega.7b00339 |
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