SIGIRR Inhibits Periodontitis-Associated Inflammation and Promotes Regeneration by Blocking Sp1 Nuclear Translocation

J Periodontal Res. 2026 Apr;61(4):406-417. doi: 10.1111/jre.70074. Epub 2026 Jan 18.

Abstract

Aim: To investigate the contribution of the Single Immunoglobulin Interleukin-1 Receptor-Related Molecule (SIGIRR), a recently described negative mediator of inflammation signaling, in experimental periodontitis pathogenesis.

Methods: A comprehensive approach was employed, including the analysis of human periodontal tissues, in vitro experiments with Periodontal ligament stem cells (PDLSCs), and validation in a rat experimental periodontitis model. The mechanistic link between LPS stimulation and SIGIRR downregulation was investigated, focusing on the p38 pathway and transcription factor Sp1. Functional effects of SIGIRR overexpression on inflammatory cytokine production were assessed.

Results: SIGIRR expression was markedly downregulated in periodontitis and LPS-stimulated PDLSCs. This downregulation was mechanistically linked to LPS activation of the p38 pathway, which impaired nuclear translocation of the transcription factor Sp1, a key positive regulator of SIGIRR transcription. SIGIRR overexpression in PDLSCs significantly attenuated LPS-induced production of pro-inflammatory cytokines (IL-6, IL-8, TNF-α). Local administration of a SIGIRR-overexpressing lentivirus in the rat experimental periodontitis model effectively reduced local pro-inflammatory cytokine levels, and promoted alveolar bone repair.

Conclusion: Together, our findings establish a unique role for p38-Sp1-SIGIRR axis in the pathogenesis of experimental periodontitis and provide evidence that SIGIRR gene therapy promises to offer an alternative option for inflammation blockade and bone repair, facilitating the development of a novel therapeutic strategy.

Keywords: inflammatory microenvironment; periodontal ligament stem cells; single Ig IL‐1‐related receptor; specific protein 1.

MeSH terms

  • Active Transport, Cell Nucleus
  • Animals
  • Cells, Cultured
  • Cytokines / metabolism
  • Disease Models, Animal
  • Down-Regulation
  • Humans
  • Inflammation* / metabolism
  • Lipopolysaccharides / pharmacology
  • Male
  • Periodontal Ligament / cytology
  • Periodontitis* / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Interleukin-1* / metabolism
  • Regeneration* / physiology
  • Signal Transduction
  • Sp1 Transcription Factor* / metabolism
  • Stem Cells / metabolism
  • Tumor Necrosis Factor-alpha / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Lipopolysaccharides
  • Sp1 Transcription Factor
  • p38 Mitogen-Activated Protein Kinases
  • Receptors, Interleukin-1
  • SIGIRR protein, human
  • Cytokines
  • Tumor Necrosis Factor-alpha