Protective effects of Wuwei Xiaodu Drink against chronic osteomyelitis through Foxp3+CD25+CD4+ Treg cells via the IL-2/STAT5 signaling pathway.
10.1016/S1875-5364(22)60146-8
- Author:
Kai HUANG
1
;
Hai-Yong REN
1
;
Bing-Yuan LIN
1
;
Yi-Yang LIU
1
;
Qiao-Feng GUO
2
Author Information
1. Department of Orthopedics, Tongde Hospital of Zhejiang Province, Hangzhou 310012, China.
2. Department of Orthopedics, Tongde Hospital of Zhejiang Province, Hangzhou 310012, China. Electronic address: hzgqf1971@163.com.
- Publication Type:Journal Article
- Keywords:
Chronic osteomyelitis;
Immunodepression;
Tregs;
Wuwei Xiaodu Drink
- MeSH:
Animals;
Forkhead Transcription Factors/metabolism*;
Interleukin-2/metabolism*;
Osteomyelitis/metabolism*;
Rats;
STAT5 Transcription Factor/metabolism*;
Signal Transduction;
T-Lymphocytes, Regulatory
- From:
Chinese Journal of Natural Medicines (English Ed.)
2022;20(3):185-193
- CountryChina
- Language:English
-
Abstract:
To explore the effectiveness and safety of a Chinese medicinal decoction Wuwei Xiaodu Drink (WWXDD) in inhibiting chronic osteomyelitis via regulatory T cells signaling. The effective constitutes of WWXDD and osteomyelitis related genes were screened. Target proteins were cross-validated using the Venny database. GO function and KEGG pathway analysis were performed for target proteins, while pharmacological network was constructed. The bone properties were analyzed by HE staining and the concentrations of immune factors were measured by ELISA. The expression of CTLA-4 and Foxp3 mRNA and STAT5, p-STAT5, CTLA-4 and Foxp3 protein were detected using Real-time PCR and Western blot, respectively. FACS was used to analyze the percentages of cells. A total of 117 genes overlapped between 785 target genes of the active compounds of WWXDD and 912 osteomyelitis related genes. Inflammation-related genes, including IL-6, TNFα, IL-1β and IL-2 showed high connection degree in the drug-compound-disease-target network. GO function and KEGG pathway analysis revealed that 117 intersection genes mainly enriched in virus infection related pathways, immune related pathways and chemokine signaling pathway. Furthermore, the development of chronic osteomyelitis was suppressed in model rats after treatment with WWXDD. Meanwhile, the concentrations of IL-2 and CD4+CD25+Foxp3 Treg percentages together with the levels of p-STAT5, CTLA-4 and Foxp3 were also down-regulated. Furthermore, IL-2 and WWXDD drug-containing serum exhibited opposite effects on regulating IL-2, IL-10, TGF-β1, Foxp3, CTLA4 and STAT5. In addition, a STAT5 phosphorylation inhibitor suppressed the expression of Foxp3 and CTLA-4. WWXDD can treat chronic osteomyelitis through suppressing the main regulating factors of Tregs and interfere its immunodepression. Our results bring a new solution for chronic osteomyelitis.
