Gold nanoparticles reduce food sensation in Caenorhabditis elegans via the voltage-gated channel EGL-19

Introduction: The increasing use of gold nanoparticles (Au NPs) in the medical field has raised concerns about the potential adverse effect of Au NPs exposure. However, it is difficult to assess the health risks of Au NPs exposure at the individual organ level using current measurement techniques. M...

Full description

Saved in:
Bibliographic Details
Main Authors: Wang, Meimei, Zhang, Zhenzhen, Sun, Ning, Yang, Baolin, Mo, Jihao, Wang, Daping, Su, Mingqin, Hu, Jian, Wang, Miaomiao, Wang, Lei
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2023
Subjects:
Online Access:https://hdl.handle.net/10356/169448
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-169448
record_format dspace
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Biological sciences
Gold Nanoparticles
RNA Sequencing
spellingShingle Science::Biological sciences
Gold Nanoparticles
RNA Sequencing
Wang, Meimei
Zhang, Zhenzhen
Sun, Ning
Yang, Baolin
Mo, Jihao
Wang, Daping
Su, Mingqin
Hu, Jian
Wang, Miaomiao
Wang, Lei
Gold nanoparticles reduce food sensation in Caenorhabditis elegans via the voltage-gated channel EGL-19
description Introduction: The increasing use of gold nanoparticles (Au NPs) in the medical field has raised concerns about the potential adverse effect of Au NPs exposure. However, it is difficult to assess the health risks of Au NPs exposure at the individual organ level using current measurement techniques. Methods: The physical and chemical properties of Au NPs were characterized by transmission electron microscope (TEM), Fourier transform infrared (FTIR), and zeta sizer. The RNA-seq data of Au NPs-exposed worms were analyzed. The food intake was measured by liquid culture and Pharyngeal pumping rate. The function of the smell and taste neurons was evaluated by the chemotaxis and avoidance assay. The activation of ASE neurons was analyzed by calcium imaging. The gene expression of ins-22 and egl-19 was obtained from the C. elegans single cell RNA-seq databases. Results: Our data analysis indicated that 62.8% of the significantly altered genes were functional in the nervous system. Notably, developmental stage analysis demonstrated that exposure to Au NPs interfered with animal development by regulating foraging behavior. Also, our chemotaxis results showed that exposure to Au NPs reduced the sensation of C. elegans to NaCl, which was consistent with the decrease in calcium transit of ASEL. Further studies confirmed that the reduced calcium transit was dependent on voltage-gated calcium channel EGL-19. The neuropeptide INS-22 was partially involved in Au NPs-induced NaCl sensation defect. Therefore, we proposed that Au NPs reduced the calcium transit in the ASEL neuron through egl-19-dependent calcium channels. It was partially regulated by the DAF-16 targeting neuropeptide INS-22. Discussion: Our results demonstrate that Au NPs affect food sensation by reducing the calcium transit in ASEL neurons, which further leads to reduced pharynx pumping and feeding defects. The toxicology studies of Au NPs from worms have great potential to guide the usage of Au NPs in the medical field such as targeted drug delivery.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Wang, Meimei
Zhang, Zhenzhen
Sun, Ning
Yang, Baolin
Mo, Jihao
Wang, Daping
Su, Mingqin
Hu, Jian
Wang, Miaomiao
Wang, Lei
format Article
author Wang, Meimei
Zhang, Zhenzhen
Sun, Ning
Yang, Baolin
Mo, Jihao
Wang, Daping
Su, Mingqin
Hu, Jian
Wang, Miaomiao
Wang, Lei
author_sort Wang, Meimei
title Gold nanoparticles reduce food sensation in Caenorhabditis elegans via the voltage-gated channel EGL-19
title_short Gold nanoparticles reduce food sensation in Caenorhabditis elegans via the voltage-gated channel EGL-19
title_full Gold nanoparticles reduce food sensation in Caenorhabditis elegans via the voltage-gated channel EGL-19
title_fullStr Gold nanoparticles reduce food sensation in Caenorhabditis elegans via the voltage-gated channel EGL-19
title_full_unstemmed Gold nanoparticles reduce food sensation in Caenorhabditis elegans via the voltage-gated channel EGL-19
title_sort gold nanoparticles reduce food sensation in caenorhabditis elegans via the voltage-gated channel egl-19
publishDate 2023
url https://hdl.handle.net/10356/169448
_version_ 1773551246176681984
spelling sg-ntu-dr.10356-1694482023-07-24T15:32:00Z Gold nanoparticles reduce food sensation in Caenorhabditis elegans via the voltage-gated channel EGL-19 Wang, Meimei Zhang, Zhenzhen Sun, Ning Yang, Baolin Mo, Jihao Wang, Daping Su, Mingqin Hu, Jian Wang, Miaomiao Wang, Lei School of Biological Sciences Science::Biological sciences Gold Nanoparticles RNA Sequencing Introduction: The increasing use of gold nanoparticles (Au NPs) in the medical field has raised concerns about the potential adverse effect of Au NPs exposure. However, it is difficult to assess the health risks of Au NPs exposure at the individual organ level using current measurement techniques. Methods: The physical and chemical properties of Au NPs were characterized by transmission electron microscope (TEM), Fourier transform infrared (FTIR), and zeta sizer. The RNA-seq data of Au NPs-exposed worms were analyzed. The food intake was measured by liquid culture and Pharyngeal pumping rate. The function of the smell and taste neurons was evaluated by the chemotaxis and avoidance assay. The activation of ASE neurons was analyzed by calcium imaging. The gene expression of ins-22 and egl-19 was obtained from the C. elegans single cell RNA-seq databases. Results: Our data analysis indicated that 62.8% of the significantly altered genes were functional in the nervous system. Notably, developmental stage analysis demonstrated that exposure to Au NPs interfered with animal development by regulating foraging behavior. Also, our chemotaxis results showed that exposure to Au NPs reduced the sensation of C. elegans to NaCl, which was consistent with the decrease in calcium transit of ASEL. Further studies confirmed that the reduced calcium transit was dependent on voltage-gated calcium channel EGL-19. The neuropeptide INS-22 was partially involved in Au NPs-induced NaCl sensation defect. Therefore, we proposed that Au NPs reduced the calcium transit in the ASEL neuron through egl-19-dependent calcium channels. It was partially regulated by the DAF-16 targeting neuropeptide INS-22. Discussion: Our results demonstrate that Au NPs affect food sensation by reducing the calcium transit in ASEL neurons, which further leads to reduced pharynx pumping and feeding defects. The toxicology studies of Au NPs from worms have great potential to guide the usage of Au NPs in the medical field such as targeted drug delivery. Published version This work was supported in part by grants from National Natural Science Foundation of China (22176002); Young Scientists Fund of the National Natural Science Foundation of China (82201315). Anhui Provincial Natural Science Foundation (2008085MB49); Open Project Fund of the Key Laboratory of the Ministry of Education for the Birth Population (JKZD20202); Funded Project of Anhui Medical University’s Research Level Improvement Program (2021xkjT004) and Funded Project of Anhui Medical University Basic and Clinical Cooperative Research Promotion Program (2021xkjT041). 2023-07-19T01:12:57Z 2023-07-19T01:12:57Z 2023 Journal Article Wang, M., Zhang, Z., Sun, N., Yang, B., Mo, J., Wang, D., Su, M., Hu, J., Wang, M. & Wang, L. (2023). Gold nanoparticles reduce food sensation in Caenorhabditis elegans via the voltage-gated channel EGL-19. International Journal of Nanomedicine, 18, 1659-1676. https://dx.doi.org/10.2147/IJN.S394666 1176-9114 https://hdl.handle.net/10356/169448 10.2147/IJN.S394666 18 2-s2.0-85151795401 18 1659 1676 en International Journal of Nanomedicine © 2023 Wang et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). application/pdf