Chen A, Zheng S
Department of Pathology, School of Medicine, Saint Louis University, St Louis, MO 63104, USA.
Br J Pharmacol. 2008 Feb;153(3):557-67. doi: 10.1038/sj.bjp.0707542. Epub 2007 Oct 29.
Gene expression of connective tissue growth factor (CTGF) is induced in activated hepatic stellate cells (HSC), the major effectors in hepatic fibrosis, and production of extracellular matrix (ECM) is consequently increased. We previously reported that curcumin, the yellow pigment in curry, suppressed ctgf expression, leading to decreased production of ECM by HSC. The purpose of this study is to evaluate signal transduction pathways involved in the curcumin suppression of ctgf expression in HSC.
Transient transfection assays were performed to evaluate effects of activation of signalling pathways on the ctgf promoter activity. Real-time PCR and Western blotting analyses were conducted to determine expression of genes.
Suppression of ctgf expression by curcumin was dose-dependently reversed by lipopolysaccharide (LPS), an NF-kappaB activator. LPS increased the abundance of CTGF and type I collagen in HSC in vitro. Activation of NF-kappaB by dominant active IkappaB kinase (IKK), or inhibition of NF-kappaB by dominant negative IkappaBalpha, caused the stimulation, or suppression of the ctgf promoter activity, respectively. Curcumin suppressed gene expression of Toll-like receptor-4, leading to the inhibition of NF-kappaB. On the other hand, interruption of ERK signalling by inhibitors or dominant negative ERK, like curcumin, reduced NF-kappaB activity and in ctgf expression. In contrast, the stimulation of ERK signalling by constitutively active ERK prevented the inhibitory effects of curcumin.
These results demonstrate that the interruption of NF-kappaB and ERK signalling by curcumin results in the suppression of ctgf expression in activated HSC in vitro.
在肝纤维化的主要效应细胞——活化肝星状细胞(HSC)中,结缔组织生长因子(CTGF)的基因表达被诱导,进而导致细胞外基质(ECM)产生增加。我们之前报道过,咖喱中的黄色色素姜黄素可抑制CTGF表达,从而使HSC产生的ECM减少。本研究的目的是评估姜黄素抑制HSC中CTGF表达所涉及的信号转导途径。
进行瞬时转染试验以评估信号通路激活对CTGF启动子活性的影响。采用实时PCR和蛋白质印迹分析来确定基因表达情况。
脂多糖(LPS,一种NF-κB激活剂)可剂量依赖性地逆转姜黄素对CTGF表达的抑制作用。LPS在体外增加了HSC中CTGF和I型胶原蛋白的丰度。显性活性IκB激酶(IKK)激活NF-κB,或显性阴性IκBα抑制NF-κB,分别导致CTGF启动子活性受到刺激或抑制。姜黄素抑制Toll样受体4的基因表达,从而抑制NF-κB。另一方面,与姜黄素一样,抑制剂或显性阴性ERK对ERK信号通路的阻断降低了NF-κB活性及CTGF表达。相反,组成型活性ERK对ERK信号通路的刺激可阻止姜黄素的抑制作用。
这些结果表明,姜黄素对NF-κB和ERK信号通路的阻断导致体外活化HSC中CTGF表达受到抑制。