Real-Time Assessment of the Antifungal Activity of Primary Human Immune Cells
筆記録
Begin with a glass-based imaging dish containing a suspension of human neutrophils — or immune cells and visualize it under a fluorescence imaging system.
Introduce genetically modified fluorescent Aspergillus reporter conidia — or fungal spores, and capture images at regular intervals up to 6 hours.
The fungal spores express red fluorescent proteins and are externally labeled with non-degradable magenta fluorophores — helping to distinguish dead cells from live ones.
During incubation, neutrophils interact with pathogen-associated molecules on conidia through pattern recognition receptors, facilitating their engulfment within a phagosome.
Later, the phagosome fuses with the enzyme-containing lysosome, forming a phagolysosome.
Inside the phagolysosome, the reactive oxygen species and enzymes degrade conidia.
During live cell imaging, at the initial time point, intense red and magenta fluorescence within the phagosome of neutrophils indicates the presence of live conidia.
Over time, a decrease in red fluorescence with the retention of magenta fluorescence indicates the degradation of conidia, confirming the antifungal activity of neutrophils.
