4.7 Article

NMR Metabolomics Reveals Metabolism-Mediated Protective Effects in Liver (HepG2) Cells Exposed to Subtoxic Levels of Silver Nanoparticles

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 17, Issue 4, Pages 1636-1646

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jproteome.7b00905

Keywords

liver (HepG2) cells; silver nanoparticles (AgNPs); ionic silver; NMR metabolomics; cell metabolism

Funding

  1. project CICECO-Aveiro Institute of Materials [FCT UID/CTM/50011/2013]
  2. project CESAM [FCT UID/AMB/50017/2013]
  3. national funds through the FCT/MEC
  4. European Regional Development Fund (FEDER) under the PT2020 Partnership Agreement
  5. FEDER through COMPETE [FCOMP-01-0124-FEDER-021456, FCT PTDC/SAU-TOX/120953/2010]
  6. national funds through FCT
  7. European Union Framework Programme for Research and Innovation HORIZON 2020, under the TEAMING grant - The Discoveries CTR [739572]
  8. FCT [SFRH/BD/79494/2011, SFRH/BPD/111736/2015, SFRH/BPD/89982/2012]
  9. Portuguese National NMR (PTNMR) Network
  10. FCT funds
  11. Fundação para a Ciência e a Tecnologia [SFRH/BD/79494/2011] Funding Source: FCT

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The expansion of biomedical and therapeutic applications of silver nanoparticles (AgNPs) raises the need to further understand their biological effects on human cells. In this work, NMR metabolomics has been applied to reveal the metabolic effects of AgNPs toward human hepatoma (HepG2) cells, which are relevant with respect to nanoparticle accumulation and detoxification. Cellular responses to widely disseminated citrate-coated AgNPs (Cit30) and to emergent biogenic AgNPs prepared using an aqueous plant extract as reducing and stabilizing agent (GS30) have been compared with a view to assess the influence of nanoparticle I coating on the metabolic effects produced. Subtoxic concentrations (IC5 and IC20) of both nanoparticle types caused profound changes in the cellular metabolome, suggesting adaptations in energy production processes (glucose metabolism and the phosphocreatine system), antioxidant defenses, protein degradation and lipid metabolism. These signatures were proposed to reflect mainly metabolism-mediated protective mechanisms and were found to be largely common to Cit30 and GS30 AgNPs, although differences in the magnitude of response, not captured by conventional cytotoxicity assessment, were detected. Overall, this study highlights the value of NMR metabolomics for revealing subtoxic biological effects and helping to understand cell-nanomaterial interactions.

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