Proanthocyanidins alleviate lipopolysaccharide-induced inflammatory response by up-regulating SIRT1 expression and inhibiting NF-κB pathway in mouse RAW264.7 macrophages.
- Author:
Yunwei WANG
1
;
Hua YANG
2
;
Zhihong WANG
2
;
Yunshu YANG
3
;
Yang LIU
4
Author Information
1. Department of Burns and Cutaneous Surgery, the First Affiliated Hospital of the Air Force Medical University, Xi'an 710032, China.
2. Department of Orthopaedics, the 80th Group Army Hospital of the PLA, Weifang 261021, China.
3. Department of Burns and Cutaneous Surgery, the First Affiliated Hospital of the Air Force Medical University, Xi'an 710032, China. *Corresponding authors, E-mail: yangys0815@qq.com.
4. Department of Burns and Cutaneous Surgery, the First Affiliated Hospital of the Air Force Medical University, Xi'an 710032, China. *Corresponding authors, E-mail: 866915@qq.com.
- Publication Type:Journal Article
- MeSH:
Animals;
Mice;
Interleukin-4;
Interleukin-6;
Lipopolysaccharides;
Macrophages;
NF-kappa B;
Proanthocyanidins;
RNA, Messenger;
Sirtuin 1/genetics*;
Tumor Necrosis Factor-alpha;
RAW 264.7 Cells
- From:
Chinese Journal of Cellular and Molecular Immunology
2023;39(10):878-883
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the role of proanthocyanidins (PC) in lipopolysaccharide (LPS)-induced inflammatory response and its possible mechanism in RAW264.7 macrophages. Methods RAW264.7 macrophages were cultured and treated with PBS and different concentrations of PC for 24 hours, followed by 1 μg/mL LPS for 6 hours. Real-time PCR was used to detect the mRNA expression of interleukin1β (IL-1β), IL-6, monocyte chemoattractant protein 1 (MCP-1), tumor necrotic factor α (TNF-α), IL-4 and arginase 1 (Arg1) in RAW264.7 macrophages. Flow cytometry was used to detect the effects of PBS group, LPS group and PC combined with LPS group on M1 and M2 polarization of macrophages. The protein expressions of silenced information regulator 1 (SIRT1), nuclear factor kappa B p65(NF-κB p65) and acetylated NF-κB p65 (Ace-p65) were detected by Western blot analysis after different concentrations of PC treatment. Co-immunoprecipitation assay was used to detect the binding effect of SIRT1 to NF-κB p65 in macrophages treated with PC. Results Compared with PBS group, the mRNA expression of macrophage pro-inflammatory cytokines IL-1β, IL-6, MCP-1 and TNF-α decreased and the mRNA expression of anti-inflammatory factors IL-4 and Arg1 increased in PC group. Compared with LPS group, PC combined with LPS group could significantly inhibit M1 polarization and promote M2 polarization of macrophages. With the increase of PC concentration, the expression of SIRT1 was up-regulated, and NF-κB p65 protein did not change significantly. The expression of Ace-p65 protein decreased significantly when treated with high concentration of PC. Conclusion PC can significantly alleviate the LPS-induced inflammatory response by up-regulating the expression of SIRT1 and inhibiting NF-κB pathway in RAW264.7 macrophages.
