Paeoniflorin ameliorates murine lupus nephritis by increasing CD4+Foxp3+ Treg cells via enhancing mTNFα-TNFR2 pathway

被引:24
作者
Liang, Chun-Ling [1 ,2 ,3 ]
Lu, Weihui [1 ,2 ,3 ]
Qiu, Feifei [1 ,2 ,3 ]
Li, Dan [4 ]
Liu, Huazhen [1 ,2 ,3 ]
Zheng, Fang [1 ,2 ,3 ]
Zhang, Qunfang [1 ,2 ,3 ]
Chen, Yuchao [1 ,2 ,3 ]
Lu, Chuanjian [1 ,2 ,3 ]
Li, Bin [4 ]
Dai, Zhenhua [1 ,2 ,3 ]
机构
[1] Guangdong Prov Acad Chinese Med Sci, Sect Immunol, 55 Nei Huan Xi Lu, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangdong Prov Acad Chinese Med Sci, Joint Immunol Program, 55 Nei Huan Xi Lu, Guangzhou 510006, Guangdong, Peoples R China
[3] Guangzhou Univ Chinese Med, Affiliated Hosp 2, Guangzhou 510006, Guangdong, Peoples R China
[4] Shanghai Jiao Tong Univ, Shanghai Inst Immunol, Dept Immunol, Sch Med, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金;
关键词
Lupus nephritis; Paeoniflorin; Macrophage; TNF-; TNFR2; Treg; REGULATORY T-CELLS; TNF-ALPHA; SUPPRESSIVE FUNCTION; DISEASE; EXPRESSION; MACROPHAGES; INFLAMMATION; RATS;
D O I
10.1016/j.bcp.2021.114434
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Treg cells are essential for re-establishing self-tolerance in lupus. However, given that direct Treg therapies may be inadequate to control autoimmunity and inflammation, a strategy of inducing or expanding endogenous Treg cells in vivo may be a good option. Macrophages are main tissue-infiltrating cells and play a role in promoting Treg differentiation while paeoniflorin (PF), a monoterpene glycoside, exhibits anti-inflammatory and immunoregulatory effects. Here, we studied the effects of PF on CD4+FoxP3+ Treg frequency and the potential mechanisms involving M2 macrophages. We demonstrated that PF ameliorated lupus nephritis in lupus-prone B6/gld mice by reducing urinary protein, serum creatinine and anti-dsDNA levels, diminishing renal cellular infiltration, improving renal immunopathology and downregulating renal gene and protein expressions of key cytokines, including IFN-?, IL-6, IL-12 and IL-23. PF also lowered the percentage of CD44highCD62Llow effector T cells while augmenting CD4+FoxP3+ Treg frequency in B6/gld mice. Importantly, PF increased TNFR2 expression on CD4+FoxP3+ Tregs, but not CD4+FoxP3- T cells, in vivo and in vitro. Furthermore, we found that CD206+ subset of F4/80+CD11b+ macrophages expressed a higher level of mTNF-? than their CD206- counterparts while PF increased mTNF-? expression on CD206+ macrophages in vitro and in vivo. In vitro studies showed that mTNF-?+ M2 macrophages were more potent in inducing Treg differentiation and proliferation than their mTNF?- counterparts, whereas the effects of mTNF-?+ M2 macrophages were largely reversed by separation of M2 macrophages using a transwell or TNFR2-blocking Ab in the culture. Finally, PF also promoted in vitro Treg generation induced by M2 macrophages. Thus, we demonstrated that mTNF?-TNFR2 interaction is a new mechanism responsible for Treg differentiation mediated by M2 macrophages. We provided the first evidence that PF may be used to treat lupus nephritis.
引用
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页数:13
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