4.8 Article

In vivo testing of gold nanoparticles using the Caenorhabditis elegans model organism

期刊

ACTA BIOMATERIALIA
卷 53, 期 -, 页码 598-609

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2017.01.080

关键词

Biological interactions; Caenorhabditis elegans; Digestive system; Enterocytes; Endocytosis; Gold nanoparticles

资金

  1. NIH Office of Research Infrastructure Programs [P40 OD010440]
  2. Spanish Ministry of Economy [MAT2015-64442-R]
  3. Spanish Ministry of Economy (Ramon y Cajal program) [RyC-2010-06082]
  4. Spanish Ministry of Economy (FPU program) [FPU12/05549]
  5. Spanish Ministry of Economy (Severo Ochoa Program - European Social Funds) [SEV-2015-0496]
  6. Generalitat de Catalunya [2014SGR213]
  7. People Program of the European Commission - European Social Fund [303630]
  8. Christian Boulin fellowship from EMBL
  9. COST Action HINT [MP1202]
  10. COST Action GENIE [BM1408-A]
  11. Spanish Ministry of Economy and Competitiveness [SEV-2015-0522]
  12. Fundacio Privada Cellex
  13. CERCA Programme from the Generalitat de Catalunya
  14. RCUK (BBSRC - Biotechnology and Biological Sciences Research Council) [BB/E025099/1]
  15. BBSRC [BB/E025099/1] Funding Source: UKRI

向作者/读者索取更多资源

Gold nanoparticles (AuNPs) are present in many man-made products and cosmetics and are also used by the food and medical industries. Tight regulations regarding the use of mammalian animals for product testing can hamper the study of the specific interactions between engineered nanoparticles and biological systems. Invertebrate models, such as the nematode Caenorhabditis elegans (C. elegans), can offer alternative approaches during the early phases of nanoparticle discovery. Here, we thoroughly evaluated the biodistribution of 11-nm and 150-nm citrate-capped AuNPs in the model organism C. elegans at multiple scales, moving from micrometric to nanometric resolution and from the organismal to cellular level. We confirmed that the nanoparticles were not able to cross the intestinal and dermal barriers. We investigated the effect of AuNPs on the survival and reproductive performance of C. elegans, and correlated these effects with the uptake of AuNPs in terms of their number, surface area, and metal mass. In general, exposure to 11-nm AuNPs resulted in a higher toxicity than the larger 150-nm AuNPs. NP aggregation inside C. elegans was determined using absorbance microspectroscopy, which allowed the plasmonic properties of AuNPs to be correlated with their confinement inside the intestinal lumen, where anatomical traits, acidic pH and the presence of biomolecules play an essential role on NP aggregation. Finally, quantitative PCR of selected molecular markers indicated that exposure to AuNPs did not significantly affect endocytosis and intestinal barrier integrity. Statement of Significance This work highlights how the simple, yet information-rich, animal model C. elegans is ideally suited for preliminary screening of nanoparticles or chemicals mitigating most of the difficulties associated with mammalian animal models, namely the ethical issues, the high cost, and time constraints. This is of particular relevance to the cosmetic, food, and pharmaceutical industries, which all have to justify the use of animals, especially during the discovery, development and initial screening phases. This work provides a detailed and thorough analysis of 11-nm and 150-nm AuNPs at multiple levels of organization (the whole organism, organs, tissues, cells and molecules). (C) 2017 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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