Fibroblasts derived C3 promotes the progression of experimental periodontitis through macrophage M1 polarization and osteoclast differentiation DOI Creative Commons
Hongchen Sun,

Feilong Ren,

Shize Zheng

et al.

Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 18, 2024

Abstract Complement C3 plays a critical role in periodontitis. However, its source, and underlying mechanisms remain unclear. In our study, by analyzing single-cell sequencing data from mouse model of periodontitis, we identified that is primarily derived periodontal fibroblasts. Subsequently, demonstrated C3a has detrimental effect ligature-induced C3ar-/- mice exhibited significantly less destruction support tissues compared to wild-type mice, characterized mild gingival tissue damage reduced alveolar bone loss. This reduction was associated with decreased production pro-inflammatory mediators osteoclast infiltration the tissues. Mechanistic studies suggested could promote macrophage polarization differentiation. Finally, patients found results observed were consistent human data. Therefore, findings clearly demonstrate destructive fibroblast-derived driven M1 These strongly feasibility C3a-targeted interventions for treatment

Language: Английский

Fibroblasts derived C3 promotes the progression of experimental periodontitis through macrophage M1 polarization and osteoclast differentiation DOI Creative Commons
Hongchen Sun,

Feilong Ren,

Shize Zheng

et al.

Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 18, 2024

Abstract Complement C3 plays a critical role in periodontitis. However, its source, and underlying mechanisms remain unclear. In our study, by analyzing single-cell sequencing data from mouse model of periodontitis, we identified that is primarily derived periodontal fibroblasts. Subsequently, demonstrated C3a has detrimental effect ligature-induced C3ar-/- mice exhibited significantly less destruction support tissues compared to wild-type mice, characterized mild gingival tissue damage reduced alveolar bone loss. This reduction was associated with decreased production pro-inflammatory mediators osteoclast infiltration the tissues. Mechanistic studies suggested could promote macrophage polarization differentiation. Finally, patients found results observed were consistent human data. Therefore, findings clearly demonstrate destructive fibroblast-derived driven M1 These strongly feasibility C3a-targeted interventions for treatment

Language: Английский

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