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Title: | Gold nanoparticles reduce food sensation in Caenorhabditis elegans via the voltage-gated channel EGL-19 | Authors: | Wang, Meimei Zhang, Zhenzhen Sun, Ning Yang, Baolin Mo, Jihao Wang, Daping Su, Mingqin Hu, Jian Wang, Miaomiao Wang, Lei |
Keywords: | Science::Biological sciences | Issue Date: | 2023 | Source: | 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 | Journal: | International Journal of Nanomedicine | Abstract: | 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. | URI: | https://hdl.handle.net/10356/169448 | ISSN: | 1176-9114 | DOI: | 10.2147/IJN.S394666 | Schools: | School of Biological Sciences | Rights: | © 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). | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | SBS Journal Articles |
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