Oligomeric proanthocyanidin derived from grape seeds inhibited NFkB signaling in activated HSC: Involvement of JNK/ERK MAPK and PI3K/Akt pathways

被引:28
作者
Jiang, Min [1 ]
Wu, Yan-Ling [1 ]
Li, Xia [1 ]
Zhang, Yu [1 ]
Xia, Kai-Li [1 ]
Cui, Ben-Wen [1 ]
Lian, Li-Hua [1 ]
Nan, Ji-Xing [1 ]
机构
[1] Yanbian Univ, Key Lab Nat Resource Changbai Mt & Funct Mol, Yanbian Univ Hosp, Minist Educ,Coll Pharm,Clin Res Ctr, Yanji 133002, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Oligomeric proanthocyanidin; Hepatic stellate cell; MAPK; PI3K; Akt; HEPATIC STELLATE CELLS; KAPPA-B; LIVER FIBROSIS; CROSS-TALK; RAT-LIVER; IN-VITRO; EXPRESSION; PROLIFERATION; FIBROGENESIS; APOPTOSIS;
D O I
10.1016/j.biopha.2017.06.105
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
In current study, we aimed to reveal the potential antifibrotic effects of oligomeric proanthocyanidin (OPC) from grape seeds on lipopolysaccharide (LPS)-activated, HSC-T6, a rat hepatic stellate cell line. HSC-T6 cells were treated with OPC 1 h prior to LPS, and then incubated for indicated time. OPC inhibited cells viability of HSC-T6 cells and decrease protein expression of collagen I, a-smooth muscle actin (alpha-SMA), tissue inhibitors of metalloproteinases I (TIMP-1) on LPS-induced HSC-T6 cells. OPC also significantly inhibited phosphorylation of LPS-stimulated phosphatidylinositol 3-kinase (PI3K), protein kinase B (Akt), extracellular signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK). Furthermore, OPC pretreatment blocked LPS-triggered nuclear factor-kappa B (NF-kappa B) translocation from cytosol to nuclear. OPC, as well as specific inhibitors of NF-kB, PI3K and JNK could effectively inhibited a-SMA and collagen I expression. In conclusion, we demonstrated that the anti-fibrotic mechanism of OPC might be involved the inhibition of HSC activation and transdifferentiation by suppressing NF-kappa B activation through JNK/ERK MAPK and PI3K/Akt phosphorylation. Thus, OPC possesses the potential inhibitory property of HSC activation through NF-kB modulation involving MAPK-PI3K/AKT pathways. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:674 / 680
页数:7
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