Effects of Erythromycin on Osteoclasts and Bone Resorption via DEL-1 Induction in Mice

Hikaru Tamura1,2,3, Tomoki Maekawa1,2, Hisanori Domon1,2

  • 1Division of Microbiology and Infectious Diseases, Graduate School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.

Insights

Erythromycin (ERM) reduces bone loss in periodontitis by increasing DEL-1 expression, which inhibits osteoclast formation. This mechanism highlights ERM's potential immunomodulatory role in treating periodontal disease.

Area of Science:

  • Immunology
  • Periodontology
  • Pharmacology

Background:

  • Macrolides, including erythromycin (ERM), are used for infectious diseases like periodontitis and possess immunomodulatory effects.
  • The precise mechanism of macrolide immunomodulation is unclear.
  • Developmental endothelial locus-1 (DEL-1) is crucial for immune homeostasis and osteoclastogenesis, and is downregulated in periodontitis.

Purpose of the Study:

  • To investigate if erythromycin's (ERM) inhibition of osteoclastogenesis is mediated by upregulating DEL-1 expression.
  • To elucidate the role of DEL-1 in ERM's effects on alveolar bone resorption in periodontitis.

Main Methods:

  • A ligature-induced periodontitis model in wild-type and DEL-1-deficient mice.
  • In vitro mechanistic studies using mouse bone marrow-derived macrophages.
  • Assessment of alveolar bone resorption and gene expression of osteoclast-related factors.

Main Results:

  • Erythromycin (ERM) treatment reduced bone loss and decreased osteoclast-related factors in wild-type mice by increasing DEL-1 expression.
  • ERM failed to suppress bone loss or alter gene expression in DEL-1-deficient mice.
  • In vitro, ERM downregulated osteoclast differentiation and calcium resorption.

Conclusions:

  • Erythromycin (ERM) induces DEL-1 in periodontal tissue, regulating osteoclastogenesis and reducing inflammatory bone resorption.
  • ERM's immunomodulatory effects in periodontitis appear to be DEL-1-dependent.
  • These findings suggest a novel therapeutic mechanism for ERM in periodontal disease.