Direct Observations of Silver Nanowire-Induced Frustrated Phagocytosis among NR8383 Lung Alveolar Macrophages.
Evgeny OgorodnikArpad KarsaiKang-Hsin WangFu-Tong LiuSu Hao LoKent E PinkertonBenjamin GilbertDominik R HaudenschildGang-Yu LiuPublished in: The journal of physical chemistry. B (2020)
The interaction of long nanowires and living cells is directly related to nanowires' nanotoxicity and health impacts. Interactions of silver nanowires (AgNWs) and macrophage cell lines (NR8383) were investigated using laser scanning confocal microscopy and single cell compression (SCC). With high-resolution imaging and mechanics measurement of individual cells, AgNW-induced frustrated phagocytosis was clearly captured in conjunction with structural and property changes of cells. While frustrated phagocytosis is known for long microwires and long carbon nanotubes, this work reports first direct observations of frustrated phagocytosis of AgNWs among living cells in situ. In the case of partial penetration of AgNWs into NR8383 cells, confocal imaging revealed actin participation at the entry sites, whose behavior differs from microwire-induced frustrated phagocytosis. The impacts of frustrated phagocytosis on the cellular membrane and cytoskeleton were also quantified by measuring the mechanical properties using SCC. Taken collectively, this study reveals the structural and property characteristics of nanowire-induced frustrated phagocytosis, which deepens our understanding of nanowire-cell interactions and nanocytotoxicity.
Keyphrases
- high resolution
- living cells
- induced apoptosis
- single cell
- room temperature
- diabetic rats
- high glucose
- fluorescent probe
- cell cycle arrest
- healthcare
- drug induced
- oxidative stress
- carbon nanotubes
- emergency department
- stem cells
- risk assessment
- high throughput
- physical activity
- rna seq
- signaling pathway
- adipose tissue
- social media
- cell therapy
- photodynamic therapy
- health information
- fluorescence imaging
- silver nanoparticles
- stress induced
- cell migration