Tobacco-derived particulates and the periodontal axis: Distinct cytotoxic and stress-related mechanisms in human gingival fibroblasts


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KOLCİ K., ÖZ E., YILDIRIM S., Azevedo R., GÜNGÖRMEK H. S., Almeida A., ...More

Scientific Reports, vol.16, no.1, 2026 (SCI-Expanded, Scopus) identifier identifier

  • Publication Type: Article / Article
  • Volume: 16 Issue: 1
  • Publication Date: 2026
  • Doi Number: 10.1038/s41598-026-35317-8
  • Journal Name: Scientific Reports
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, Chemical Abstracts Core, MEDLINE, Directory of Open Access Journals
  • Keywords: Autophagosome formation, Inflammation, Oxidative stress, Periodontal diseases, Tobacco products, Total particulate matter
  • Karadeniz Technical University Affiliated: Yes

Abstract

Tobacco products vary widely in their chemical composition and potential harm, yet their impact on oral tissue remains insufficiently characterized. This study comparatively investigated the cytotoxic, oxidative, and inflammatory responses, along with apoptotic/necrotic cell death, autophagosome formation, and tissue remodeling capacity, in human gingival fibroblasts (hGFs) exposed to total particulate matter (TPM) derived from a conventional cigarette (TPM-c) and a heated tobacco product (TPM-h). TPMs were chemically characterized by inductively coupled plasma mass spectrometry (ICP-MS) for heavy metal content. TPM-c induced notable cytotoxicity, necrosis, and impaired wound healing compared to TPM-h, although both products compromised hGF viability and function. In addition, higher levels of Cadmium (Cd), Lead (Pb), and Zinc (Zn) were detected in TPM-c. Triggered vascular endothelial growth factor-A (VEGF-A) upregulation as a defensive reaction to cellular stress was observed in hGFs via TPM-c, while TPM-h reduced autophagic response via Microtubule-associated protein 1 A/1 B-light chain 3-phosphatidyl ethanolamine conjugate/LC3-II (LC3β) expression. Both TPMs elevated interleukin-6 (IL-6) release, notably at intermediate and high doses. In summary, TPM-c demonstrated a greater capacity than TPM-h to induce cytotoxicity, oxidative and inflammatory damage, and disrupted tissue remodeling. Nonetheless, TPM-h was not devoid of toxicity, eliciting pro-inflammatory/ angiogenic responses concentration-dependently. These findings highlight the necessity of further investigation into the long-term effects of emerging tobacco products on periodontal disease progression and development.