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.

Inflammation
|January 21, 2022
PubMed

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.