Periodontitis promotes bacterial extracellular vesicle-induced neuroinflammation in the brain and trigeminal ganglion

PLoS Pathog. 2023 Oct 23;19(10):e1011743. doi: 10.1371/journal.ppat.1011743. eCollection 2023 Oct.

Abstract

Gram-negative bacteria derived extracellular vesicles (EVs), also known as outer membrane vesicles, have attracted significant attention due to their pathogenic roles in various inflammatory diseases. We recently demonstrated that EVs secreted by the periodontopathogen Aggregatibacter actinomycetemcomitans (Aa) can cross the blood-brain barrier (BBB) and that their extracellular RNA cargo can promote the secretion of proinflammatory cytokines, such as IL-6 and TNF-α, in the brain. To gain more insight into the relationship between periodontal disease (PD) and neuroinflammatory diseases, we investigated the effect of Aa EVs in a mouse model of ligature-induced PD. When EVs were administered through intragingival injection or EV-soaked gel, proinflammatory cytokines were strongly induced in the brains of PD mice. The use of TLR (Toll-like receptor)-reporter cell lines and MyD88 knockout mice confirmed that the increased release of cytokines was triggered by Aa EVs via TLR4 and TLR8 signaling pathways and their downstream MyD88 pathway. Furthermore, the injection of EVs through the epidermis and gingiva resulted in the direct retrograde transfer of Aa EVs from axon terminals to the cell bodies of trigeminal ganglion (TG) neurons and the subsequent activation of TG neurons. We also found that the Aa EVs changed the action potential of TG neurons. These findings suggest that EVs derived from periodontopathogens such as Aa might be involved in pathogenic pathways for neuroinflammatory diseases, neuropathic pain, and other systemic inflammatory symptoms as a comorbidity of periodontitis.

MeSH terms

  • Animals
  • Blood-Brain Barrier / metabolism
  • Cytokines / metabolism
  • Extracellular Vesicles* / metabolism
  • Mice
  • Mice, Knockout
  • Myeloid Differentiation Factor 88 / metabolism
  • Neuroinflammatory Diseases
  • Periodontal Diseases* / metabolism
  • Periodontitis* / metabolism
  • Trigeminal Ganglion

Substances

  • Myeloid Differentiation Factor 88
  • Cytokines

Grants and funding

This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) and funded by the Korean Government (MSIT 2017R1A5A2015391) to YL and H-JL, (2021R1A2C1004512) to H-JL, and (2020R1A2C1009364) to YL. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.