Benzo[a]pyrene exacerbates bone destruction by inhibiting Treg differentiation, impairing Treg function and promoting osteoclastogenesis in rats with collagen-induced arthritis

  • Ecotoxicol Environ Saf. 2026 May:316:120135. doi: 10.1016/j.ecoenv.2026.120135.
Tingting Deng  1 ,  Xing Wang  2 ,  Tong Shi  3 ,  Yi Jiao  4 ,  Qishun Geng  3 ,  Zhaoran Wang  3 ,  Cheng Xiao  5
Affiliations
  • 1. Institute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China.
  • 2. Department of Nephrology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
  • 3. Institute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China; China-Japan Friendship Hospital (Institute of Clinical Medical Sciences), Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.
  • 4. Institute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China; Department of Emergency, China-Japan Friendship Hospital, Beijing, China.
  • 5. Institute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China; Department of Emergency, China-Japan Friendship Hospital, Beijing, China. Electronic address: [email protected].
PMID: 41980281 DOI: 10.1016/j.ecoenv.2026.120135
Abstract

Background: Emerging evidence has shown that exposure to polycyclic aromatic hydrocarbons (PAHs) is a risk factor for rheumatoid arthritis (RA). Benzo[a]pyrene (BaP), a representative PAH congener, exacerbates the development of collagen-induced arthritis (CIA) in animal models. However, the underlying mechanisms, particularly those involving the immune dynamic and functional plasticity of regulatory T cells (Tregs), remain largely unknown.

Method: In this study, a rat CIA model was used to evaluate the effect of BaP on RA onset following intervention with the Aryl Hydrocarbon Receptor (AHR) antagonist CH223191. The effects of BaP on the differentiation of regulatory T cells (Tregs) and osteoclasts (OCs) were subsequently assessed. Furthermore, the significance of the BaP-AHR axis in the pathogenesis of RA was determined using reverse transcriptionpolymerase chain reaction (RTPCR), flow cytometry and immunohistochemistry. Finally, the influence of BaP on osteoclastogenesis was confirmed through the coculture of Tregs and bone marrow-derived monocytes (BMMs).

Results: Our findings indicate that BaP significantly exacerbates joint inflammation and bone destruction in rats with CIA. Mechanistically, BaP not only suppresses the differentiation of Tregs but also impairs the ability of Tregs to secrete anti-inflammatory cytokines, such as IL-10 and TGF-β. Furthermore, BaP actively promotes the differentiation of OCs. These detrimental effects are predominantly mediated by activation of the AHR signalling pathway.

Conclusion: These results reveal the cellular and molecular mechanisms of BaP during RA pathogenesis, providing novel therapeutic targets for RA.

Keywords
Aryl hydrocarbon receptor; Benzo[a]pyrene; IL-10 and TGF-β; Osteoclasts; Regulatory T cells; Rheumatoid arthritis.
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