摘要
肝星状细胞 (HSCs) 的活化是肝纤维化发病机制中一个重要因素,代表着诸如在HSCs中刺激促纤维化基因的叉头蛋白f1(Foxf1) 等转录因子抑制和激活的交互作用。在此,我们评估脂质肝特异性传递系统 (DBTC) 合理地将 Foxf1 siRNA特定传递至HSCs,调查其对原发性HSCs和LX-2细胞以及在胆管结扎诱发的继发性胆汁淤积鼠模型中的抗纤维化潜能。Foxf1沉默减少HSCs的增殖能力和减毒收缩。小鼠的DBTC-lipoplexes系统性管理足以特定地使在不同肝细胞型中表达的基因沉默。我们使用活体免疫荧光显微镜确认了Cy3示踪的DBTC特定传递至肝脏,尤其是HSCs。使用DBTC-lipoplexes反复治疗导致siRNA介导的Foxf1在BDL后不久就沉默,并最终减弱纤维化进程。减少HSC活化确实能改善肝损伤,表现为坏死面积大幅削减和细胞外基质沉积。我们的研究结果表明,Foxf1可能作为一个靶点基因来扰乱肝纤维化进程,DBTC可能为治疗性RNA的HSC特定传递提供一个可行、有效的工具。
关键词: 胆汁淤积,慢性肝病,活体显微镜,lipoplex,鼠,沉默。
Current Gene Therapy
Title:Foxf1 siRNA Delivery to Hepatic Stellate Cells by DBTC Lipoplex Formulations Ameliorates Fibrosis in Livers of Bile Duct Ligated Mice
Volume: 15 Issue: 3
Author(s): Kerstin Abshagen, Malte Brensel, Berit Genz, Kira Roth, Maria Thomas, Volker Fehring, Ute Schaeper and Brigitte Vollmar
Affiliation:
关键词: 胆汁淤积,慢性肝病,活体显微镜,lipoplex,鼠,沉默。
摘要: Activation of hepatic stellate cells (HSCs) is a key event in pathogenesis of liver fibrosis and represents an orchestral interplay of inhibiting and activating transcription factors like forkhead box f1 (Foxf1), being described to stimulate pro-fibrogenic genes in HSCs. Here, we evaluated a lipidbased liver-specific delivery system (DBTC) suitable to transfer Foxf1 siRNA specifically to HSCs and examined its antifibrotic potential on primary HSCs and LX-2 cells as well as in a murine model of bile duct ligation (BDL)-induced secondary cholestasis. Foxf1 silencing reduced proliferation capacity and attenuated contractility of HSCs. Systemic administration of DBTC-lipoplexes in mice was sufficient to specifically silence genes expressed in different liver cell types. Using intravital and immunofluorescence microscopy we confirmed the specific delivery of Cy3-labeled DBTC to the liver, and particularly to HSCs. Repeated treatment with DBTC-lipoplexes resulted in siRNA-mediated silencing of Foxf1 early after BDL and finally attenuated progression of the fibrotic process. Decreased HSC activation in-effect ameliorated liver injury as shown by substantial reduction of necrotic area and deposition of extracellular matrix. Our findings suggest that Foxf1 may serve as a target gene to disrupt progression of liver fibrosis and DBTC might provide a potentially feasible and effective tool for HSC-specific delivery of therapeutic RNA.
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Kerstin Abshagen, Malte Brensel, Berit Genz, Kira Roth, Maria Thomas, Volker Fehring, Ute Schaeper and Brigitte Vollmar , Foxf1 siRNA Delivery to Hepatic Stellate Cells by DBTC Lipoplex Formulations Ameliorates Fibrosis in Livers of Bile Duct Ligated Mice, Current Gene Therapy 2015; 15 (3) . https://dx.doi.org/10.2174/1566523215666150126114634
DOI https://dx.doi.org/10.2174/1566523215666150126114634 |
Print ISSN 1566-5232 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5631 |
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