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      Comprehensive phenotyping and transcriptome profiling to study nanotoxicity in C. elegans

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          Abstract

          Engineered nanoparticles are used at an increasing rate in both industry and medicine without fully understanding their impact on health and environment. The nematode Caenorhabditis elegans is a suitable model to study the toxic effects of nanoparticles as it is amenable to comprehensive phenotyping, such as locomotion, growth, neurotoxicity and reproduction. In this study, we systematically evaluated the effects of silver (Ag) and five metal oxide nanoparticles: SiO 2, CeO 2, CuO, Al 2O 3 and TiO 2. The results showed that Ag and SiO 2 exposures had the most toxic effects on locomotion velocity, growth and reproduction, whereas CeO 2, Al 2O 3 and CuO exposures were mostly neurotoxic. We further performed RNAseq to compare the gene expression profiles underlying Ag and SiO 2toxicities. Gene set enrichment analyses revealed that exposures to Ag and SiO 2consistently downregulated several biological processes (regulations in locomotion, reproductive process and cell growth) and pathways (neuroactive ligand-receptor interaction, wnt and MAPK signaling, etc.), with opposite effects on genes involved in innate immunity. Our results contribute to mechanistic insights into toxicity of Ag and SiO 2 nanoparticles and demonstrated that C. elegans as a valuable model for nanotoxicity assessment.

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          Most cited references53

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          Hsp70 chaperones: Cellular functions and molecular mechanism

          Abstract. Hsp70 proteins are central components of the cellular network of molecular chaperones and folding catalysts. They assist a large variety of protein folding processes in the cell by transient association of their substrate binding domain with short hydrophobic peptide segments within their substrate proteins. The substrate binding and release cycle is driven by the switching of Hsp70 between the low-affinity ATP bound state and the high-affinity ADP bound state. Thus, ATP binding and hydrolysis are essential in vitro and in vivo for the chaperone activity of Hsp70 proteins. This ATPase cycle is controlled by co-chaperones of the family of J-domain proteins, which target Hsp70s to their substrates, and by nucleotide exchange factors, which determine the lifetime of the Hsp70-substrate complex. Additional co-chaperones fine-tune this chaperone cycle. For specific tasks the Hsp70 cycle is coupled to the action of other chaperones, such as Hsp90 and Hsp100.
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            TSC2 integrates Wnt and energy signals via a coordinated phosphorylation by AMPK and GSK3 to regulate cell growth.

            Mutation in the TSC2 tumor suppressor causes tuberous sclerosis complex, a disease characterized by hamartoma formation in multiple tissues. TSC2 inhibits cell growth by acting as a GTPase-activating protein toward Rheb, thereby inhibiting mTOR, a central controller of cell growth. Here, we show that Wnt activates mTOR via inhibiting GSK3 without involving beta-catenin-dependent transcription. GSK3 inhibits the mTOR pathway by phosphorylating TSC2 in a manner dependent on AMPK-priming phosphorylation. Inhibition of mTOR by rapamycin blocks Wnt-induced cell growth and tumor development, suggesting a potential therapeutic value of rapamycin for cancers with activated Wnt signaling. Our results show that, in addition to transcriptional activation, Wnt stimulates translation and cell growth by activating the TSC-mTOR pathway. Furthermore, the sequential phosphorylation of TSC2 by AMPK and GSK3 reveals a molecular mechanism of signal integration in cell growth regulation.
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              Finding function in novel targets: C. elegans as a model organism.

              Despite its apparent simplicity, the nematode worm Caenorhabditis elegans has developed into an important model for biomedical research, particularly in the functional characterization of novel drug targets that have been identified using genomics technologies. The cellular complexity and the conservation of disease pathways between C. elegans and higher organisms, together with the simplicity and cost-effectiveness of cultivation, make for an effective in vivo model that is amenable to whole-organism high-throughput compound screens and large-scale target validation. This review describes how C. elegans models can be used to advance our understanding of the molecular mechanisms of drug action and disease pathogenesis.
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                Author and article information

                Contributors
                Journal
                PeerJ
                PeerJ
                peerj
                peerj
                PeerJ
                PeerJ Inc. (San Diego, USA )
                2167-8359
                27 February 2020
                2020
                : 8
                : e8684
                Affiliations
                [1 ]Institute of Parasitology, McGill University , Montreal, Canada
                [2 ]Department of Animal Science, McGill University , Montreal, Quebec, Canada
                Article
                8684
                10.7717/peerj.8684
                7049462
                be6403b1-5bd2-4222-8e83-be668d68d6d2
                ©2020 Viau et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.

                History
                : 10 October 2019
                : 4 February 2020
                Funding
                Funded by: Fonds Québécois de la Recherche sur la Nature et les Technologies (FQRNT), Genome Canada, Genome Quebec
                Funded by: The Natural Sciences and Engineering Research Council of Canada (NSERC) Discovery Grant
                This study was supported by the Fonds Québécois de la Recherche sur la Nature et les Technologies (FQRNT), Genome Canada, Genome Quebec and the Natural Sciences and Engineering Research Council of Canada (NSERC) Discovery Grant. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Bioinformatics
                Molecular Biology
                Toxicology
                Ecotoxicology

                c. elegans, ag, sio2, nanoparticles, locomotion velocity, growth inhibition, reproduction, neurotoxicity, rnaseq

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