Thymosin α1 alleviates pulpitis by inhibiting ferroptosis of dental pulp cells.
10.1038/s41368-025-00394-4
- Author:
Jie WU
1
;
Qimei GONG
1
;
Wenxuan LIU
1
;
Aijia CHEN
1
;
Zekai LIAO
1
;
Yihua HUANG
1
;
Wenkai JIANG
2
;
Zhongchun TONG
3
Author Information
1. Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
2. State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration & National Clinical Research Center for Oral Diseases & Shaanxi Key Laboratory of Stomatology, Department of Operative Dentistry & Endodontics, School of Stomatology, Fourth Military Medical University, Xi'an, China. JiangW6@cardiff.ac.uk.
3. Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China. tongzhch@mail.sysu.edu.cn.
- Publication Type:Journal Article
- MeSH:
Ferroptosis/drug effects*;
Dental Pulp/drug effects*;
Animals;
Pulpitis/pathology*;
Rats;
Thymalfasin/pharmacology*;
Humans;
Male;
Thymosin/pharmacology*;
Disease Models, Animal;
Rats, Sprague-Dawley
- From:
International Journal of Oral Science
2025;17(1):68-68
- CountryChina
- Language:English
-
Abstract:
Tooth pulpitis is a prevalent oral disorder. Understanding the underlying mechanisms of pulpitis and developing effective treatment strategies hold great significance. Ferroptosis has recently emerged as a new form of cell death, but the role of ferroptosis in pulpitis remains largely unknown. In our study, single-cell RNA sequencing (scRNA-seq) was used to identify cellular heterogeneity between 3 pulpitis tissue and 3 healthy pulp tissue, and explored ferroptosis occurrence in pulpitis tissue and inflamed dental pulp cells (DPCs). In scRNA-seq, 40 231 cells (Pulpitis: 17 814; Healthy pulp: 22 417) were captured, and visualized into 12 distinct cell clusters. Differentially expressed ferroptosis-related genes (DE-FRGs) were almost presented in each cluster in pulpitis vs healthy pulp. ROS and Fe2+ levels significantly rose, and immunohistochemistry showed low expression of GPX4 and high expression of PTGS2 in pulpitis. In LPS-stimulated DPCs, thymosin α1 increased the expression of GPX4 and FTL, and decreased expression of TNF-α, IL-1β, IL-6, and Fe2+ levels. In rat pulpitis models, both prothymosin α (PTMA, precursor of thymosin α1) gelatin sponge placed at the hole of pulp (LPS-P(gs)) and PTMA injection in pulp (LPS-P(i)) significantly reduced infiltration of inflammatory cells and expression of PTGS2, and increased the expression of GPX4. In RNA sequencing, the expression of DE-FRGs were reversed when thymosin α1 were added in LPS-stimulated DPCs. Collectively, single-cell atlas reveals cellular heterogeneity between pulpitis and healthy pulp, and ferroptosis occurrence in pulpitis. Thymosin α1 may reduce ferroptosis in DPCs to alleviate pulpitis and thus potentially has the ability to treat pulpitis.
