Geniposide ameliorates atherosclerosis by regulating macrophage polarization via perivascular adipocyte-derived CXCL14

被引:11
|
作者
He, Peikun [1 ]
Wang, Hao [1 ]
Cheng, Saibo [1 ]
Hu, Fang [1 ]
Zhang, Lifang [1 ]
Chen, Weicong [1 ]
Xu, Yuling [2 ]
Zhang, Yaxin [1 ]
Gu, Yuyan [1 ]
Li, Zhaoyong [1 ]
Jin, Yao [1 ]
Liu, Xiaoyu [3 ]
Jia, Yuhua [1 ,4 ]
机构
[1] Southern Med Univ, Sch Tradit Chinese Med, Guangzhou, Guangdong, Peoples R China
[2] Fujian Med Univ, Coll Hlth, Fuzhou, Fujian, Peoples R China
[3] Southern Med Univ, Pingshan Gen Hosp, Shenzhen Pingshan Dist Med Healthcare Grp, Shenzhen, Guangdong, Peoples R China
[4] Southern Med Univ, Sch Tradit Chinese Med, 1023 Shatai Rd, Guangzhou 510515, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Geniposide; Atherosclerosis; Macrophage polarization; Perivascular adipose tissue; CXCL14; INFLAMMATION; PHENOTYPE; FAT; MECHANISMS; ARTERIES;
D O I
10.1016/j.jep.2023.116532
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Gardenia jasminoides Ellis is a traditional Chinese medicine that has been used for treatment of various diseases, including atherosclerosis by clearing heat and detoxication. Geniposide is considered as the effective compounds responsible for the therapeutic efficacy of Gardenia jasminoides Ellis against atherosclerosis.Aim of the study: To investigate the effect of geniposide on atherosclerosis burden and plaque macrophage po-larization, with focus on its potential impact on CXCL14 expression by perivascular adipose tissue (PVAT).Materials and methods: ApoE-/-mice fed a western diet (WD) were used to model atherosclerosis. In vitro cultures of mouse 3T3-L1 preadipocytes and RAW264.7 macrophages were used for molecular assays.Results: The results revealed that geniposide treatment reduced atherosclerotic lesions in ApoE-/-mice, and this effect was correlated with increased M2 and decreased M1 polarization of plaque macrophages. Of note, geni-poside increased the expression of CXCL14 in PVAT, and both the anti-atherosclerotic effect of geniposide, as well as its regulatory influence on macrophage polarization, were abrogated upon in vivo CXCL14 knockdown. In line with these findings, exposure to conditioned medium from geniposide-treated 3T3-L1 adipocytes (or to recombinant CXCL14 protein) enhanced M2 polarization in interleukin-4 (IL-4) treated RAW264.7 macrophages, and this effect was negated after CXCL14 silencing in 3T3-L1 cells.Conclusion: In summary, our findings suggest that geniposide protects ApoE-/-mice against WD-induced atherosclerosis by inducing M2 polarization of plaque macrophages via enhanced expression of CXCL14 in PVAT. These data provide novel insights into PVAT paracrine function in atherosclerosis and reaffirm geniposide as a therapeutic drug candidate for atherosclerosis treatment.
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页数:13
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