Department of Gastroenterology, Shanghai First People's Hospital, Shanghai Jiaotong University School of Medicine, No.100 Haining Road, Shanghai, China.
Int J Med Sci. 2012;9(5):370-9. doi: 10.7150/ijms.4395. Epub 2012 Jul 10.
To investigate the effects of 18α-glycyrrhetinic acid (18α-GA) on the expression of type I and III collagen in human and rat hepatic stellate cells (HSC) and to explore the role of TGF-β1/Smad signaling pathway involved.
Following 18α-GA treatment, the cell viability and cell growth were detected to determine the optimal concentration of 18α-GA. The expressions of TGF-β1/Smad signaling-related genes including type I and III collagen in human and rat HSCs before and after 18α-GA treatment were measured by real time PCR. The expression of related proteins was verified by western blot assay. The phosphorylation level of Smad2 and Smad3 was detected by immunocytochemistry. The DNA binding activities of SP-1, AP-1 and NF-κB were measured by both EMSA and ArrayStar transcription factor activity assay.
18α-GA could decrease the mRNA and protein expression of Smad3, type I and III collagen, increase the Smad7 expression in human and rat HSCs (P<0.05), and reduce phosphorylation level of Smad3 at 24 h and 48 h after treatment. The DNA binding activities of transcription factors were suppressed by 18α-GA in human and rat HSCs at 24 h, and the activities reduced in a time dependent manner with the lowest activities at 48 h, especially for SP-1.
18α-GA could inhibit the mRNA and protein expression of type I and III collagen in human and rat HSCs, which may be attributed to down-regulation of Smad3, up-regulation of Smad7, and inhibition of DNA binding activities of SP-1, AP-1 and NF-κB.
研究 18α-甘草次酸(18α-GA)对人及大鼠肝星状细胞(HSC)I 型和 III 型胶原表达的影响,并探讨其涉及的 TGF-β1/Smad 信号通路的作用。
用 18α-GA 处理细胞后,通过细胞活力和细胞生长检测确定 18α-GA 的最佳浓度。用实时 PCR 检测人及大鼠 HSCs 经 18α-GA 处理前后 TGF-β1/Smad 信号相关基因包括 I 型和 III 型胶原的表达。用 Western blot 检测相关蛋白的表达。用免疫细胞化学检测 Smad2 和 Smad3 的磷酸化水平。用 EMSA 和 ArrayStar 转录因子活性检测试剂盒检测 SP-1、AP-1 和 NF-κB 的 DNA 结合活性。
18α-GA 可降低人及大鼠 HSCs 中 Smad3、I 型和 III 型胶原的 mRNA 和蛋白表达,增加 Smad7 的表达(P<0.05),并降低处理后 24 h 和 48 h Smad3 的磷酸化水平。18α-GA 可抑制人及大鼠 HSCs 中 24 h 的转录因子的 DNA 结合活性,且随时间呈下降趋势,在 48 h 时活性最低,特别是 SP-1。
18α-GA 可抑制人及大鼠 HSCs 中 I 型和 III 型胶原的 mRNA 和蛋白表达,其机制可能与下调 Smad3、上调 Smad7 以及抑制 SP-1、AP-1 和 NF-κB 的 DNA 结合活性有关。