Azithromycin and Chloramphenicol Diminish Neutrophil Extracellular Traps (NETs) Release.
Weronika BystrzyckaAneta Manda-HandzlikSandra SieczkowskaAneta MoskalikUrszula DemkowOlga CiepielaPublished in: International journal of molecular sciences (2017)
Neutrophils are one of the first cells to arrive at the site of infection, where they apply several strategies to kill pathogens: degranulation, respiratory burst, phagocytosis, and release of neutrophil extracellular traps (NETs). Antibiotics have an immunomodulating effect, and they can influence the properties of numerous immune cells, including neutrophils. The aim of this study was to investigate the effects of azithromycin and chloramphenicol on degranulation, apoptosis, respiratory burst, and the release of NETs by neutrophils. Neutrophils were isolated from healthy donors by density-gradient centrifugation method and incubated for 1 h with the studied antibiotics at different concentrations (0.5, 10 and 50 μg/mL-azithromycin and 10 and 50 μg/mL-chloramphenicol). Next, NET release was induced by a 3 h incubation with 100 nM phorbol 12-myristate 13-acetate (PMA). Amount of extracellular DNA was quantified by fluorometry, and NETs were visualized by immunofluorescent microscopy. Degranulation, apoptosis and respiratory burst were assessed by flow cytometry. We found that pretreatment of neutrophils with azithromycin and chloramphenicol decreases the release of NETs. Moreover, azithromycin showed a concentration-dependent effect on respiratory burst in neutrophils. Chloramphenicol did not affect degranulation, apoptosis nor respiratory burst. It can be concluded that antibiotics modulate the ability of neutrophils to release NETs influencing human innate immunity.
Keyphrases
- cell cycle arrest
- high frequency
- endoplasmic reticulum stress
- oxidative stress
- cell death
- flow cytometry
- induced apoptosis
- endothelial cells
- single molecule
- respiratory tract
- optical coherence tomography
- photodynamic therapy
- pi k akt
- high resolution
- high throughput
- cell proliferation
- high speed
- multidrug resistant
- mass spectrometry
- gram negative