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法尼醇X受体-小异源二聚体伴侣调节级联可调节肝星状细胞中组织金属蛋白酶抑制剂-1和基质金属蛋白酶的表达,并促进肝纤维化的消退。

A farnesoid x receptor-small heterodimer partner regulatory cascade modulates tissue metalloproteinase inhibitor-1 and matrix metalloprotease expression in hepatic stellate cells and promotes resolution of liver fibrosis.

作者信息

Fiorucci Stefano, Rizzo Giovanni, Antonelli Elisabetta, Renga Barbara, Mencarelli Andrea, Riccardi Luisa, Orlandi Stefano, Pruzanski Mark, Morelli Antonio, Pellicciari Roberto

机构信息

Dept. of Clinical and Experimental Medicine, University of Perugia, Policlinico Monteluce, Via E. Dal Pozzo, 06122 Perugia, Italy.

出版信息

J Pharmacol Exp Ther. 2005 Aug;314(2):584-95. doi: 10.1124/jpet.105.084905. Epub 2005 Apr 28.

Abstract

The farnesoid X receptor (FXR) is expressed by and regulates hepatic stellate cells (HSCs). In the present study, we investigated whether 6-ethyl chenodeoxycholic acid (6-ECDCA or INT-747), a semisynthetic derivative of chenodeoxycholic acid (CDCA), modulates tissue metalloproteinase inhibitor (TIMP)-1 and matrix metalloprotease (MMP)-2 expression/activity in HSCs and in the liver of rats rendered cirrhotic by 4-week administration of CCl(4). Exposure of HSCs to FXR ligands increases small heterodimer partner (SHP) mRNA by 3-fold and reduces basal and thrombin-stimulated expression of alpha1(I)collagen, alpha-smooth muscle actin (alpha-SMA), TIMP-1, and TIMP-2 by approximately 60 to 70%, whereas it increased matrix metalloprotease (MMP)-2 activity by 2-fold. In coimmunoprecipitation, electromobility shift, and transactivation experiments, FXR activation/overexpression caused a SHP-dependent inhibition of JunD binding to its consensus element in the TIMP-1 promoter. Inhibition of TIMP-1 expression by SHP overexpression enhanced the sensitivity of HSCs to proapoptogenic stimuli. Administration of 3 mg/kg 6-ECDCA, but not 15 mg/kg ursodeoxycholic acid, resulted in early (3-5-day) induction of SHP and prevention of early up-regulation of TIMP-1 mRNA induced by CCl(4). In the prevention protocol, 4-week administration of 6-ECDCA reduced alpha1(I)collagen, alpha-SMA, and TIMP-1 mRNA by 60 to 80%, whereas it increased MMP-2 activity by 5-fold. In the resolution protocol, administration of 3 mg/kg 6-ECDCA promoted liver fibrosis resolution and increased the apoptosis of nonparenchyma liver cells. By demonstrating that a FXR-SHP regulatory cascade promotes the development of a quiescent phenotype and increases apoptosis of HSCs, this study establishes that FXR ligands may be beneficial in treatment of liver fibrosis.

摘要

法尼酯X受体(FXR)由肝星状细胞(HSC)表达并对其起调节作用。在本研究中,我们探究了鹅去氧胆酸(CDCA)的半合成衍生物6-乙基鹅去氧胆酸(6-ECDCA或INT-747)是否能调节组织金属蛋白酶抑制剂(TIMP)-1和基质金属蛋白酶(MMP)-2在HSC以及经4周四氯化碳(CCl₄)处理诱导肝硬化的大鼠肝脏中的表达/活性。将HSC暴露于FXR配体可使小异源二聚体伴侣(SHP)mRNA增加3倍,并使α1(I)型胶原、α-平滑肌肌动蛋白(α-SMA)、TIMP-1和TIMP-2的基础表达以及凝血酶刺激后的表达降低约60%至70%,而MMP-2活性则增加2倍。在免疫共沉淀、电泳迁移率变动分析及反式激活实验中,FXR激活/过表达导致SHP依赖性抑制JunD与TIMP-1启动子中其共有元件的结合。SHP过表达对TIMP-1表达的抑制增强了HSC对促凋亡刺激的敏感性。给予3mg/kg的6-ECDCA,但不给予15mg/kg的熊去氧胆酸,可导致SHP的早期(3至5天)诱导,并预防CCl₄诱导的TIMP-1 mRNA早期上调。在预防方案中,4周给予6-ECDCA可使α1(I)型胶原、α-SMA和TIMP-1 mRNA降低60%至80%,而MMP-2活性增加5倍。在消退方案中,给予3mg/kg的6-ECDCA可促进肝纤维化消退,并增加非实质肝细胞的凋亡。通过证明FXR-SHP调节级联促进静止表型的发展并增加HSC的凋亡,本研究证实FXR配体可能对肝纤维化治疗有益。

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