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

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 a...

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Veröffentlicht in:Journal of ethnopharmacology 2023-10, Vol.314, p.116532-116532, Article 116532
Hauptverfasser: He, Peikun, Wang, Hao, Cheng, Saibo, Hu, Fang, Zhang, Lifang, Chen, Weicong, Xu, Yuling, Zhang, Yaxin, Gu, Yuyan, Li, Zhaoyong, jin, Yao, Liu, Xiaoyu, Jia, Yuhua
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container_title Journal of ethnopharmacology
container_volume 314
creator He, Peikun
Wang, Hao
Cheng, Saibo
Hu, Fang
Zhang, Lifang
Chen, Weicong
Xu, Yuling
Zhang, Yaxin
Gu, Yuyan
Li, Zhaoyong
jin, Yao
Liu, Xiaoyu
Jia, Yuhua
description 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. To investigate the effect of geniposide on atherosclerosis burden and plaque macrophage polarization, with focus on its potential impact on CXCL14 expression by perivascular adipose tissue (PVAT). 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. 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, geniposide 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. 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. [Display omitted]
doi_str_mv 10.1016/j.jep.2023.116532
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Geniposide is considered as the effective compounds responsible for the therapeutic efficacy of Gardenia jasminoides Ellis against atherosclerosis. To investigate the effect of geniposide on atherosclerosis burden and plaque macrophage polarization, with focus on its potential impact on CXCL14 expression by perivascular adipose tissue (PVAT). 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. 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, geniposide 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. 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. [Display omitted]</description><identifier>ISSN: 0378-8741</identifier><identifier>EISSN: 1872-7573</identifier><identifier>DOI: 10.1016/j.jep.2023.116532</identifier><identifier>PMID: 37149071</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>adipocytes ; Adipocytes - metabolism ; adipose tissue ; Animals ; Apolipoproteins E - genetics ; Atherosclerosis ; Atherosclerosis - metabolism ; Chemokines, CXC - metabolism ; Chemokines, CXC - therapeutic use ; CXCL14 ; drugs ; Gardenia jasminoides ; Geniposide ; heat ; interleukin-4 ; Macrophage polarization ; macrophages ; Macrophages - metabolism ; Mice ; Mice, Inbred C57BL ; Oriental traditional medicine ; Perivascular adipose tissue ; Plaque, Atherosclerotic - drug therapy ; protective effect ; therapeutics ; Western diets</subject><ispartof>Journal of ethnopharmacology, 2023-10, Vol.314, p.116532-116532, Article 116532</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. 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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. 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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Geniposide is considered as the effective compounds responsible for the therapeutic efficacy of Gardenia jasminoides Ellis against atherosclerosis. To investigate the effect of geniposide on atherosclerosis burden and plaque macrophage polarization, with focus on its potential impact on CXCL14 expression by perivascular adipose tissue (PVAT). 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. 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, geniposide 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. 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subjects adipocytes
Adipocytes - metabolism
adipose tissue
Animals
Apolipoproteins E - genetics
Atherosclerosis
Atherosclerosis - metabolism
Chemokines, CXC - metabolism
Chemokines, CXC - therapeutic use
CXCL14
drugs
Gardenia jasminoides
Geniposide
heat
interleukin-4
Macrophage polarization
macrophages
Macrophages - metabolism
Mice
Mice, Inbred C57BL
Oriental traditional medicine
Perivascular adipose tissue
Plaque, Atherosclerotic - drug therapy
protective effect
therapeutics
Western diets
title Geniposide ameliorates atherosclerosis by regulating macrophage polarization via perivascular adipocyte-derived CXCL14
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