Doxycycline inhibits TREM-1 induction by Porphyromonas gingivalis

Nagihan Bostanci1, Georgios N Belibasakis

  • 1Oral Translational Research, Institute of Oral Biology, Center of Dental Medicine, University of Zürich, Switzerland. nagihan.bostanci@zzm.uzh.ch

Insights

Subantimicrobial doses of doxycycline (SDD) reduce the expression and release of triggering receptor expressed on myeloid cells 1 (TREM-1) induced by Porphyromonas gingivalis. This anti-inflammatory effect may explain SDD

Area of Science:

  • Immunology
  • Microbiology
  • Periodontology

Background:

  • Triggering receptor expressed on myeloid cells 1 (TREM-1) amplifies pro-inflammatory cytokine production.
  • Porphyromonas gingivalis is linked to periodontal and systemic inflammation.
  • Subantimicrobial doses of doxycycline (SDD) possess anti-inflammatory properties used in periodontal therapy.

Purpose of the Study:

  • To investigate the impact of SDD on P. gingivalis-induced TREM-1 expression and secretion.
  • To evaluate the anti-inflammatory effects of SDD in a cellular model of periodontal disease.

Main Methods:

  • Exposure of MonoMac-6 cells to P. gingivalis.
  • Treatment with varying concentrations of SDD.
  • Measurement of TREM-1 gene expression, soluble TREM-1 release, and interleukin-8 secretion.

Main Results:

  • P. gingivalis significantly increased TREM-1 expression and soluble TREM-1 release.
  • SDD (2-10 μg/mL) inhibited P. gingivalis-induced TREM-1 expression and release within 4 hours.
  • SDD reduced P. gingivalis-induced interleukin-8 secretion.

Conclusions:

  • SDD effectively inhibits P. gingivalis-induced TREM-1.
  • Inhibition of TREM-1 may contribute to the anti-inflammatory effects of SDD in periodontal disease.
  • SDD could potentially modulate systemic inflammatory responses.

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