Epigallocatechin‐3‐gallate ameliorates lipopolysaccharide‐induced acute thymus involution in mice via AMPK/Sirt1 pathway

脂多糖 安普克 内卷(密宗) 生物 没食子酸 内分泌学 内科学 免疫学 药理学 微生物学 生物化学 磷酸化 医学 蛋白激酶A 神经科学 意识
作者
Qing Su,Shu‐Ping Yang,J S Guo,Yi‐Ren Rong,Yun Sun,Yurong Chai
出处
期刊:Microbiology and Immunology [Wiley]
卷期号:68 (8): 281-293 被引量:2
标识
DOI:10.1111/1348-0421.13159
摘要

The thymus, a site to culture the naïve T lymphocytes, is susceptible to atrophy or involution due to aging, inflammation, and oxidation. Epigallocatechin-3-gallate (EGCG) has been proven to possess anti-inflammatory, antioxidant, and antitumor activity. Here, we investigate the effects of EGCG on thymic involution induced by lipopolysaccharide (LPS), an endotoxin derived from Gram-negative bacteria. The methodology included an in vivo experiment on female Kunming mice exposed to LPS and EGCG. Morphological assessment of thymic involution, immunohistochemical detection, and thymocyte subsets analysis by flow cytometry were further carried out to evaluate the potential role of EGCG on the thymus. As a result, we found that EGCG alleviated LPS-induced thymic atrophy, increased mitochondrial membrane potential and superoxide dismutase levels, and decreased malondialdehyde and reactive oxygen species levels. In addition, EGCG pre-supplement restored the ratio of thymocyte subsets, the expression of autoimmune regulator, sex-determining region Y-box 2, and Nanog homebox, and reduced the number of senescent cells and collagen fiber deposition. Western blotting results indicated that EGCG treatment elevated LPS-induced decrease in pAMPK, Sirt1 protein expression. Collectively, EGCG relieved thymus architecture and function damaged by LPS via regulation of AMPK/Sirt1 signaling pathway. Our findings may provide a new strategy on protection of thymus from involution caused by LPS by using EGCG. And EGCG might be considered as a potential agent for the prevention and treatment of thymic involution.
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