Pterostilbene, a Bioactive Component of Blueberries, Alleviates Renal Interstitial Fibrosis by Inhibiting Macrophage-Myofibroblast Transition

被引:18
作者
Feng, Yanhuan [1 ]
Guo, Fan [1 ]
Mai, Hongxia [1 ,2 ]
Liu, Jing [1 ]
Xia, Zijing [1 ]
Zhu, Guonian [3 ]
Zhang, Jinhang [4 ]
Ma, Liang [1 ]
Fu, Ping [1 ]
机构
[1] Sichuan Univ, West China Hosp, Kidney Res Inst, Div Nephrol & Natl Clin,Res Ctr Geriatr, Chengdu 610041, Peoples R China
[2] Lanzhou Univ Second Hosp, Dept Nephrol, Lanzhou 730030, Peoples R China
[3] Sichuan Univ, West China Hosp, Core Facil, Chengdu 610041, Peoples R China
[4] Sichuan Univ, West China Hosp, Lab Clin Pharm & Adverse Drug React, Chengdu 610041, Peoples R China
来源
AMERICAN JOURNAL OF CHINESE MEDICINE | 2020年 / 48卷 / 07期
关键词
Pterostilbene; Renal Interstitial Fibrosis; Macrophage-Myofibroblast Transition; CXCL10; INTERFERON-INDUCIBLE PROTEIN-10; HEPATITIS-C VIRUS; RESVERATROL; EXPRESSION; IP-10; ACTIVATION; CXCL10;
D O I
10.1142/S0192415X20500858
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Pterostilbene (PTB) is a derivative of resveratrol present in grapes and blueberries. PTB is structurally similar to resveratrol, possessing properties such as being analgesic, anti-aging, antidiabetic, anti-inflammatory, anti-obesity, anti-oxidation, cholesterol-reductive, and neuroprotective. However, there have not been reports on the effect of PTB on macrophage-myofibroblast transition (MMT) induced fibrosis in kidney. In this study, we investigated the antifibrotic effects of PTB on the in vivo mouse unilateral ureteral obstruction (UUO) model and in vitro MMT cells. Kidneys subjected to UUO with PTB treatment were collected for the investigation of PTB mediating MMT derived renal interstitial fibrosis. We conducted kidney RNA-seq transcriptomes and TGF-beta 1-induced bone marrow-derived macrophages assays to determine the mechanisms of PTB. We found that PTB treatment suppressed the interstitial fibrosis in UUO mice. PTB also attenuated the number of MMT cells in vivo and in vitro. The transcriptomic analysis showed that CXCL10 may play a central role in the process of PTB-treated renal fibrosis. The siRNA-mediated CXCL10 knockdown decreased the number of MMT cells in TGF-beta 1-induced bone marrow-derived macrophages. Our results suggested that PTB attenuated renal interstitial fibrosis by mediating MMT by regulating transcriptional activity of CXCL10.
引用
收藏
页码:1715 / 1729
页数:15
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