Steroid Receptor Coactivator 3 Is Required for Clearing Bacteria and Repressing Inflammatory Response in Escherichia coli-Induced Septic Peritonitis

被引:29
作者
Chen, Qiang [1 ,2 ]
Chen, Tenghui [1 ]
Xu, Yixiang [1 ]
Zhu, Jingwei [1 ]
Jiang, Yuan [1 ]
Zhao, Yang [1 ]
Xu, Jianming [3 ]
Yu, Chundong [1 ]
机构
[1] Xiamen Univ, Minist Educ Cell Biol & Tumor Cell Engn, Sch Life Sci, Key Lab, Xiamen 361005, Fujian, Peoples R China
[2] Xiamen Univ, Affiliated Hosp 1, Xiamen 361005, Fujian, Peoples R China
[3] Baylor Coll Med, Dept Mol & Cell Biol, Houston, TX 77030 USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
INNATE IMMUNE-RESPONSE; OXYGEN SPECIES ROS; GENE-EXPRESSION; INDUCED APOPTOSIS; SEPSIS; INFECTION; PHAGOCYTOSIS; ACTIVATION; CANCER; SRC-3;
D O I
10.4049/jimmunol.0903802
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Steroid receptor coactivator 3 (SRC-3) is a multifunctional protein that plays an important role in regulation of bacterial LPS-induced inflammation. However, its involvement in host defense against bacterial infection remains unclear. In this study, we used SRC-3 knockout mice to assess the role of SRC-3 in antibacterial defense in Escherichia coli-induced septic peritonitis. After E. coli bacteria were injected i.p., SRC-3-deficient mice exhibited excessive local and systemic inflammatory responses and more severe bacterial burdens, leading to a significantly higher mortality compared with wild-type mice. Peritoneal macrophages of SRC-3-deficient mice showed a decrease in bacterial phagocytosis in culture and an increase in apoptosis, which was consistent with the defective bacterial clearance observed in SRC-3-deficient mice. Accordingly, SRC-3 null macrophages expressed much lower levels of scavenger receptor A, the antioxidant enzyme catalase, and antiapoptotic gene Bcl-2. Collectively, our data demonstrate that SRC-3 is important not only in modulating the local and systemic inflammation but also in intensifying bacterial clearance, which highlights a pivotal role of SRC-3 in the host defense system against bacterial infection. The Journal of Immunology, 2010, 185: 5444-5452.
引用
收藏
页码:5444 / 5452
页数:9
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