Total glucosides of paeony attenuated functional maturation of dendritic cells via blocking TLR4/5 signaling in vivo

被引:76
作者
Zhou, Zhou [1 ]
Lin, Jinpiao [1 ]
Huo, Rongfen [1 ]
Huang, Wenkang [2 ]
Zhang, Jian [2 ]
Wang, Li [1 ]
Sun, Yue [1 ]
Shen, Baihua [1 ]
Li, Ningli [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Inst Immunol, Inst Med Sci, Shanghai 200025, Peoples R China
[2] Shanghai Jiao Tong Univ, Key Lab Cell Differentiat & Apoptosis, Dept Pathophysiol, Natl Minist Educ,Sch Med, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金;
关键词
Total glucosides of paeony; Dendritic cells; Maturation; Toll like receptors; COLLAGEN-INDUCED ARTHRITIS; FIBROBLAST-LIKE SYNOVIOCYTES; RHEUMATOID-ARTHRITIS; TLR4-MD-2; COMPLEX; EPITHELIAL-CELLS; T-CELLS; DIFFERENTIATION; PAEONIFLORIN; RATS; MECHANISMS;
D O I
10.1016/j.intimp.2012.07.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It is well known that dendritic cells (DCs) play a critical role in the initiation and development of an immune response. Inhibitory effect on DC maturation alters immune-mediated inflammatory reaction in vivo. Total glucosides of paeony (TGP) are active compounds extracted from the roots of Paeonia lactiflora and have been widely used to ameliorate inflammation in therapy for autoimmune diseases. However, whether TGP act on DC maturation remains unknown. In this study, we investigated the effect of TGP on DC maturation in ovalbumin (OVA) immunized mice. Ear inflammation was inhibited by TGP (150 mg kg(-1), i.p. x 11 days) obviously. The antigen presenting capacity of DC derived from TGP-treated mice was arrested. Meanwhile, OVA specific T cell proliferation was inhibited. In addition, we found that maturation of DCs was decreased by TGP treatment. Furthermore. OVA specific T cell proliferation was rescued by the adoptive transfer of mature DCs (mDCs) into TGP treated OVA-challenged mice. The research on the mechanism showed that TGP significantly inhibited activation of TLR4/5 singling. All these results demonstrated that TGP inhibited DC maturation and function by selectively blocking TLR4/5 activation in vivo, which in turn leads to reduce immune-mediated inflammation in vivo, adding a novel mechanism and therapeutic target of TGP for inflammatory and autoimmune disease treatment. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:275 / 282
页数:8
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