4.8 Article

Toxicogenomic Responses of the Model Organism Caenorhabditis elegans to Gold Nanoparticles

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 46, 期 7, 页码 4115-4124

出版社

AMER CHEMICAL SOC
DOI: 10.1021/es2033108

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资金

  1. National Science Foundation (NSF)
  2. Environmental Protection Agency (EPA) under NSF [EF-0830093]
  3. Center for the Environmental Implications of Nano Technology (CENT), EPA [RD-83457401]
  4. Transatlantic Initiative for Nanotechnology and the Environment (TINE)
  5. University of Kentucky Office
  6. EU [CP-FP 247739]
  7. NERC [NE/H013644/1] Funding Source: UKRI
  8. Natural Environment Research Council [ceh010023, NE/H013644/1] Funding Source: researchfish

向作者/读者索取更多资源

We used Au nanoparticles (Au-NPs) as a model for studying particle-specific effects of manufactured nanomaterials (MNMs) by examining the toxicogenomic responses in a model soil organism, Caenorhabditis elegans. Global genome expression for nematodes exposed to 4-nm citrate-coated Au-NPs at the LC10 level (5.9 mg.L-1) revealed significant differential expression of 797 genes. The levels of expression for five genes (apl-1, dyn-1, act-5, abu-11, and hsp-4) were confirmed independently with qRT-PCR Seven common biological pathways associated with 38 of these genes were identified. Up-regulation of 26 pqn/abu genes from noncanonical unfolded protein response (UPR) pathway and molecular chaperones (hsp-16.1, hsp-70, hsp-3, and hsp-4) were observed and are likely indicative of endoplasmic reticulum stress. Significant increase in sensitivity to Au-NPs in a mutant from noncanonical UPR (pqn-5) suggests possible involvement of the genes from this pathway in a protective mechanism against Au-NPs. Significant responses to Au-NPs in endocytosis mutants (chc-1 and rme-2) provide evidence for endocytosis pathway being induced by Au-NPs. These results demonstrate that Au-NPs are bioavailable and cause adverse effects to C. elegans by activating both general and specific biological pathways. The experiments with mutants further support involvement of several of these pathways in Au-NP toxicity and/or detoxification.

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