Exposure to silver nanoparticles affects viability and function of natural killer cells, mostly via the release of

Loretta Müller1, Selina K Steiner2, Laura Rodriguez-Lorenzo3

  • 1University Children's Hospital Basel, Spitalstrasse 33, 4056, Basel, Switzerland. Loretta.mueller@ukbb.ch.

Insights

Silver nanoparticles (AgNPs) impair natural killer (NK) cell function, reducing their viability and cytotoxic potential. This immune modulation by AgNPs warrants further investigation for potential health risks.

Area of Science:

  • Immunology
  • Nanotoxicology
  • Cell Biology

Background:

  • Natural killer (NK) cells are crucial for innate immunity, viral defense, and tumor surveillance.
  • NK cell activity is regulated by surface receptors and involves cytokine release and cell killing.
  • Increasing use of engineered nanoparticles, like silver nanoparticles (AgNPs), raises concerns about human exposure and potential health effects.

Purpose of the Study:

  • To investigate the effects of 20-nm silver nanoparticles (AgNPs) on human NK cell viability, phenotype, and function.
  • To compare the impact of AgNPs with silver ions (Ag+) on NK cells.
  • To assess the potential immunomodulatory risks associated with AgNP exposure.

Main Methods:

  • Human peripheral blood NK cells were exposed overnight to varying concentrations of AgNPs and Ag+ ions.
  • Analysis included cell viability, surface receptor expression (inhibitory and activating), intracellular markers, cytokine release, and cytotoxic potential.
  • Polyriboinosinic-polyribocytidylic acid stimulation was used to assess NK cell cytotoxic capacity.

Main Results:

  • AgNP exposure, unlike Ag+ ions, significantly reduced NK cell viability and cytotoxic potential.
  • AgNPs increased the expression of the inhibitory receptor CD159a.
  • Both AgNPs and Ag+ ions altered the expression of activating receptors (CD335, CD16, CD314).

Conclusions:

  • Exposure to AgNPs alters NK cell function and phenotype.
  • AgNPs may pose a risk for modulating human immune responses.
  • Further research is needed to fully understand the immunotoxicological implications of AgNP exposure.

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