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C. elegans-on-a-chip for in situ and in vivo Ag nanoparticles’ uptake and toxicity assay

Nanomaterials are extensively used in consumer products and medical applications, but little is known about their environmental and biological toxicities. Moreover, the toxicity analysis requires sophisticated instruments and labor-intensive experiments. Here we report a microfluidic chip incorporat...

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Autores principales: Kim, Jin Ho, Lee, Seung Hwan, Cha, Yun Jeong, Hong, Sung Jin, Chung, Sang Kug, Park, Tai Hyun, Choi, Shin Sik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5220357/
https://www.ncbi.nlm.nih.gov/pubmed/28067319
http://dx.doi.org/10.1038/srep40225
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author Kim, Jin Ho
Lee, Seung Hwan
Cha, Yun Jeong
Hong, Sung Jin
Chung, Sang Kug
Park, Tai Hyun
Choi, Shin Sik
author_facet Kim, Jin Ho
Lee, Seung Hwan
Cha, Yun Jeong
Hong, Sung Jin
Chung, Sang Kug
Park, Tai Hyun
Choi, Shin Sik
author_sort Kim, Jin Ho
collection PubMed
description Nanomaterials are extensively used in consumer products and medical applications, but little is known about their environmental and biological toxicities. Moreover, the toxicity analysis requires sophisticated instruments and labor-intensive experiments. Here we report a microfluidic chip incorporated with the nematode Caenorhabditis elegans that rapidly displays the changes in body growth and gene expression specifically responsive to the silver nanoparticles (AgNPs). C. elegans were cultured in microfluidic chambers in the presence or absence of AgNPs and were consequently transferred to wedge-shaped channels, which immobilized the animals, allowing the evaluation of parameters such as length, moving distance, and fluorescence from the reporter gene. The AgNPs reduced the length of C. elegans body, which was easily identified in the channel of chip. In addition, the decrease of body width enabled the worm to advance the longer distance compared to the animal without nanoparticles in a wedge-shaped channel. The transgenic marker DNA, mtl-2::gfp was highly expressed upon the uptake of AgNPs, resulting in green fluorescence emission. The comparative investigation using gold nanoparticles and heavy-metal ions indicated that these parameters are specific to AgNPs. These results demonstrate that C. elegans-on-a-chip has a great potential as a rapid and specific nanoparticle detection or nanotoxicity assessment system.
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spelling pubmed-52203572017-01-11 C. elegans-on-a-chip for in situ and in vivo Ag nanoparticles’ uptake and toxicity assay Kim, Jin Ho Lee, Seung Hwan Cha, Yun Jeong Hong, Sung Jin Chung, Sang Kug Park, Tai Hyun Choi, Shin Sik Sci Rep Article Nanomaterials are extensively used in consumer products and medical applications, but little is known about their environmental and biological toxicities. Moreover, the toxicity analysis requires sophisticated instruments and labor-intensive experiments. Here we report a microfluidic chip incorporated with the nematode Caenorhabditis elegans that rapidly displays the changes in body growth and gene expression specifically responsive to the silver nanoparticles (AgNPs). C. elegans were cultured in microfluidic chambers in the presence or absence of AgNPs and were consequently transferred to wedge-shaped channels, which immobilized the animals, allowing the evaluation of parameters such as length, moving distance, and fluorescence from the reporter gene. The AgNPs reduced the length of C. elegans body, which was easily identified in the channel of chip. In addition, the decrease of body width enabled the worm to advance the longer distance compared to the animal without nanoparticles in a wedge-shaped channel. The transgenic marker DNA, mtl-2::gfp was highly expressed upon the uptake of AgNPs, resulting in green fluorescence emission. The comparative investigation using gold nanoparticles and heavy-metal ions indicated that these parameters are specific to AgNPs. These results demonstrate that C. elegans-on-a-chip has a great potential as a rapid and specific nanoparticle detection or nanotoxicity assessment system. Nature Publishing Group 2017-01-09 /pmc/articles/PMC5220357/ /pubmed/28067319 http://dx.doi.org/10.1038/srep40225 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kim, Jin Ho
Lee, Seung Hwan
Cha, Yun Jeong
Hong, Sung Jin
Chung, Sang Kug
Park, Tai Hyun
Choi, Shin Sik
C. elegans-on-a-chip for in situ and in vivo Ag nanoparticles’ uptake and toxicity assay
title C. elegans-on-a-chip for in situ and in vivo Ag nanoparticles’ uptake and toxicity assay
title_full C. elegans-on-a-chip for in situ and in vivo Ag nanoparticles’ uptake and toxicity assay
title_fullStr C. elegans-on-a-chip for in situ and in vivo Ag nanoparticles’ uptake and toxicity assay
title_full_unstemmed C. elegans-on-a-chip for in situ and in vivo Ag nanoparticles’ uptake and toxicity assay
title_short C. elegans-on-a-chip for in situ and in vivo Ag nanoparticles’ uptake and toxicity assay
title_sort c. elegans-on-a-chip for in situ and in vivo ag nanoparticles’ uptake and toxicity assay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5220357/
https://www.ncbi.nlm.nih.gov/pubmed/28067319
http://dx.doi.org/10.1038/srep40225
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