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Visualizing Macrophage Extracellular Traps Using Confocal Microscopy
Published on: October 19, 2017
Enhanced Responsive Formation of Extracellular Traps in Macrophages Previously Exposed to Porphyromonas gingivalis
Yu-Jie Liu1,2,3, Jia-Lu Chen1,2,3, Zi-Bo Fu1,2,3
1Department of Periodontology, The Affiliated Stomatological Hospital of Nanjing Medical University, No. 1 Shanghai Road, Nanjing, 210029, China.
Abstract:
Tolerance is defined to be a hyporesponsive state following repeated stimulations with bacteria or their virulence factors and has potential impacts on the development of periodontitis. Recently, macrophages have been reported to release chromatin and antimicrobial peptides to form extracellular traps upon bacterial or chemical stimulations. Thus, we explored the roles and mechanisms of tolerance induced by Porphyromonas gingivalis (P. gingivalis) in macrophage extracellular traps (METs). Tolerance in peritoneal macrophages from mice was triggered by repeated P. gingivalis stimulation. METs were observed using fluorescence microscopy, and the levels of extracellular DNA were determined by microplate reader assays. The expression of p-RAF, p-MEK, and p-ERK was examined by Western blot, and reactive oxygen species (ROS) production was explored using flow cytometry. Moreover, the levels of intracellular Ca2+ were also determined by confocal microscopy to identify the possible mechanisms related to the changes in METs in P. gingivalis-pretreated macrophages. Repeated P. gingivalis stimulation contributed to the formation of METs and increased levels of extracellular DNA (p < 0.05). ROS generation and RAF/MEK/ERK phosphorylation were decreased in P. gingivalis-pretreated macrophages compared with non-pretreated cells (p < 0.05), which was inconsistent with the changes in METs. However, in P. gingivalis-pretreated macrophages, the levels of intracellular Ca2+ were significantly increased compared with the single stimulation group. Additionally, inhibition of intracellular Ca2+ resulted in a decrease in the levels of extracellular DNA in P. gingivalis-pretreated cells (p < 0.05). Taken together, P. gingivalis-pretreated macrophages released more METs, possibly related to the increased levels of intracellular Ca2+.
Insights
Repeated stimulation with Porphyromonas gingivalis induces tolerance in macrophages, leading to increased macrophage extracellular traps (METs). This phenomenon is linked to elevated intracellular calcium levels, not reduced ROS or RAF/MEK/ERK phosphorylation.
Area of Science:
- Immunology
- Cell Biology
- Microbiology
Background:
- Tolerance, a hyporesponsive state after repeated bacterial stimulation, impacts periodontitis development.
- Macrophages release extracellular traps (chromatin, antimicrobial peptides) upon stimulation.
- Porphyromonas gingivalis (P. gingivalis) is a key bacterium implicated in periodontitis.
Purpose of the Study:
- To investigate the role and mechanisms of tolerance induced by P. gingivalis in macrophage extracellular traps (METs).
- To explore how P. gingivalis affects MET formation and the underlying cellular signaling pathways.
Main Methods:
- Peritoneal macrophages from mice were repeatedly stimulated with P. gingivalis to induce tolerance.
- METs and extracellular DNA levels were quantified using fluorescence microscopy and microplate assays.
- Western blot analyzed RAF/MEK/ERK phosphorylation; flow cytometry assessed ROS production; confocal microscopy measured intracellular Ca2+.
Main Results:
- Repeated P. gingivalis stimulation increased MET formation and extracellular DNA levels.
- ROS generation and RAF/MEK/ERK phosphorylation were decreased in tolerant macrophages.
- Intracellular Ca2+ levels were significantly increased in P. gingivalis-pretreated macrophages.
- Inhibiting intracellular Ca2+ reduced extracellular DNA release in tolerant cells.
Conclusions:
- P. gingivalis-induced tolerance in macrophages enhances MET release.
- Increased intracellular Ca2+ is a key mechanism driving enhanced MET formation in tolerant macrophages.
- These findings offer insights into the immunopathology of periodontitis and potential therapeutic targets.
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