Fuzheng Huayu recipe, a traditional Chinese compound herbal medicine, attenuates renal interstitial fibrosis via targeting the miR-21/PTEN/AKT axis

被引:15
作者
Wang, Qing-lan [1 ,2 ,3 ]
Tao, Yan-yan [3 ]
Xie, Hong-dong [3 ]
Liu, Cheng-hai [2 ,3 ]
Liu, Ping [2 ,3 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Coll Basic Med Sci, Teaching & Res Dept Clin & Class Med, Shanghai 201203, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Shanghai Municipal Educ Comm, E Inst, Shanghai 210203, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Inst Liver Dis, Shuguang Hosp, Shanghai 210203, Peoples R China
来源
JOURNAL OF INTEGRATIVE MEDICINE-JIM | 2020年 / 18卷 / 06期
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Fuzheng Huayu recipe; Chinese herbal medicine; Renal interstitial fibrosis; miR-21; PTEN; AKT; microRNA; EPITHELIAL-MESENCHYMAL TRANSITION; ANGIOTENSIN-II; MICRORNAS; TRANSCRIPTION; FIBROBLASTS; INHIBITION; PATHWAYS;
D O I
10.1016/j.joim.2020.08.006
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Objective: MicroRNAs (miRNAs) may be viable targets for treating renal interstitial fibrosis (RIF). Fuzheng Huayu recipe (FZHY), a traditional Chinese compound herbal medicine, is often used in China to treat fibrosis. This study sought to assess the mechanisms through which FZHY influences miRNAs to treat RIF. Methods: RIF was induced in rats by mercury chloride and treated with FZHY. Hydroxyproline content, Masson's staining and type I collagen expression were used to evaluate renal collagen deposition. Renal miRNA profiles were evaluated using a miRNA microarray. Those miRNAs that were differentially expressed following FZHY treatment were identified and subjected to bioinformatic analyses. The miR-21 target gene phosphatase and tensin homolog (PTEN) expression and AKT phosphorylation in kidney tissues were assessed via Western blotting. In addition, HK-2 human proximal tubule epithelial cells were treated using angiotensin II (Ang-II) to induce epithelial-to-mesenchymal transition (EMT), followed by FZHY exposure. miR-21 and PTEN expressions were evaluated via quantitative reverse transcription-polymerase chain reaction (qRT-PCR), while E-cadherin and alpha-smooth muscle actin (alpha-SMA) expressions were assessed by immunofluorescent staining and qRT-PCR. Western blotting was used to assess PTEN and AKT phosphorylation. Results: FZHY significantly decreased kidney collagen deposition, hydroxyproline content and type I collagen level. The miRNA microarray identified 20 miRNAs that were differentially expressed in response to FZHY treatment. Subsequent bioinformatic analyses found that miR-21 was the key fibrosis-related miRNA regulated by FZHY. FZHY also decreased PTEN expression and AKT phosphorylation in fibrotic kidneys. Results from in vitro tests also suggested that FZHY promoted E-cadherin upregulation and inhibited alpha-SMA expression in Ang-II-treated HK-2 cells, effectively reversing Ang-II-mediated EMT. We also determined that FZHY reduced miR-21 expression, increased PTEN expression and decreased AKT phosphorylation in these cells. Conclusion: miR-21 is the key fibrosis-related miRNA regulated by FZHY. The ability of FZHY to modulate miR-21/PTEN/AKT signaling may be a viable approach for treating RIF. (C) 2020 Shanghai Changhai Hospital. Published by ELSEVIER B.V. All rights reserved.
引用
收藏
页码:505 / 513
页数:9
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