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Published on: June 2, 2023
The effects of silver nanoparticles on RAW 264.7. Macrophages and human whole blood cell cultures
Kim Leigh Lategan1, Chavon Rene Walters2, Edmund John Pool3
1UWC, Robert Sobukwe Road, Bellville, South Africa, Cape Town, 7535.
Abstract:
Silver nanoparticles (AgNPs) are commonly found in consumer products due to their antimicrobial properties. This study evaluated the effects of AgNPs on the murine macrophage cell line RAW 264.7 and human whole blood cell cultures (WBCs). Effects of AgNPs on RAW cells were assessed in the presence or absence of lipopolysaccharide (LPS). Effects of AgNPs on WBCs were monitored under basal conditions and in the presence of either LPS or phytohaemmagglutinin (PHA). AgNPs were cytotoxic to WBCs at 250 μg/ml. Under basal conditions, RAW cells ≥ 62.5. μg/ml and WBCs > 25 μg/ml AgNPs induced biomarkers associated with inflammation. Under LPS stimulated conditions, 250 μg/ml AgNP inhibited biomarkers associated with inflammation for both cultures. Under basal conditions, and in the presence of 250 μg/ml AgNP, WBCs produced acquired immune system cytokines IL-10 and IFNγ. IL-10 synthesis by WBCs was partially inhibited by 250 μg/ml AgNP in the presence of PHA. Proteome profiles of RAW cell supernatants show that AgNPs modulate biomarkers associated with inflammation. WBCs proteome analysis shows modulation of biomarkers associated with anti-inflammatory effects.
Insights
Silver nanoparticles (AgNPs) can cause inflammation in immune cells at low doses but may reduce inflammation under certain conditions. AgNPs also impact cytokine production and proteome profiles in both cell types.
Area of Science:
- Immunology
- Nanotechnology
- Toxicology
Background:
- Silver nanoparticles (AgNPs) are widely used in consumer products for their antimicrobial properties.
- Understanding the biological effects of AgNPs on human and animal immune cells is crucial.
Purpose of the Study:
- To investigate the effects of AgNPs on murine macrophage RAW 264.7 cells and human whole blood cells (WBCs).
- To assess AgNP-induced cytotoxicity, inflammation biomarkers, cytokine production, and proteome modulation.
Main Methods:
- Exposure of RAW 264.7 cells and WBCs to varying concentrations of AgNPs under basal, lipopolysaccharide (LPS), or phytohaemagglutinin (PHA) stimulated conditions.
- Assessment of cytotoxicity, inflammatory biomarkers, and cytokine profiles (IL-10, IFNγ).
- Proteome analysis of cell supernatants to identify modulated proteins.
Main Results:
- AgNPs exhibited cytotoxicity to WBCs at 250 μg/ml.
- AgNPs induced inflammation biomarkers in RAW cells (≥ 62.5 μg/ml) and WBCs (> 25 μg/ml) under basal conditions.
- At 250 μg/ml, AgNPs inhibited inflammation biomarkers in LPS-stimulated cultures.
- WBCs produced IL-10 and IFNγ under basal conditions with AgNPs, with partial IL-10 inhibition by PHA.
- Proteome analysis revealed AgNP-induced modulation of inflammation and anti-inflammatory biomarkers.
Conclusions:
- AgNPs exert dose-dependent effects on immune cells, inducing inflammation at lower doses and potentially mitigating it at higher, stimulated doses.
- AgNPs influence the production of key immune cytokines and alter cellular proteomes, indicating complex immunomodulatory effects.
- Further research is needed to fully elucidate the toxicological and therapeutic potential of AgNPs in biological systems.
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