Su Pei-Fen, Staniforth Vanisree, Li Chin-Jin, Wang Chien-Yu, Chiao Ming-Tsang, Wang Sheng-Yang, Shyur Lie-Fen, Yang Ning-Sun
Agricultural Biotechnology Research Center, Academia Sinica, Nankang, Taipei, 11529, Taiwan, ROC.
J Biomed Sci. 2008 Nov;15(6):813-22. doi: 10.1007/s11373-008-9266-7. Epub 2008 Jul 13.
To investigate the immunomodulatory activities of phytocompounds for potential therapeutics, we devised an in vivo, transgenic, human cytokine gene promoter assay using defined epidermal skin cells as test tissue. Test compounds were topically applied to mouse skin before or after gene gun transfection, using a cytokine gene promoter-driven luciferase reporter. Croton oil, an inflammation inducer, induced transgenic GM-CSF and TNF-alpha promoter activities in skin epidermis 6-fold and 3.4-fold, respectively; however, it produced a less than 1.5-fold and 1.7-fold change in IL-1beta and IL-18 promoter activity, respectively. The phytocompound shikonin drastically inhibited inducible GM-CSF promoter activity. However, a fraction of Dioscorea batatas extract significantly increased the GM-CSF promoter activity in normal and inflamed skin. Shikonin suppressed the transcriptional activity of GM-CSF promoter by inhibiting the binding of TFIID protein complex (TBP) to TATA box. Our results demonstrate that this in vivo transgenic promoter activity assay system is cytokine gene-specific, and highly responsive to pro-inflammatory or anti-inflammatory stimuli. Currently it is difficult to profile the expression and cross-talk of various types of cytokines in vivo. This investigation has established a bona fide in vivo, in situ, immune tissue system for research into cytokine response to inflammation.
为了研究植物化合物在潜在治疗方面的免疫调节活性,我们设计了一种体内转基因人细胞因子基因启动子检测方法,使用特定的表皮皮肤细胞作为测试组织。在基因枪转染之前或之后,将测试化合物局部应用于小鼠皮肤,使用细胞因子基因启动子驱动的荧光素酶报告基因。炎症诱导剂巴豆油分别诱导皮肤表皮中转基因GM-CSF和TNF-α启动子活性增加6倍和3.4倍;然而,它分别使IL-1β和IL-18启动子活性变化小于1.5倍和1.7倍。植物化合物紫草素显著抑制可诱导的GM-CSF启动子活性。然而,薯蓣提取物的一部分在正常和炎症皮肤中显著增加了GM-CSF启动子活性。紫草素通过抑制TFIID蛋白复合物(TBP)与TATA盒的结合来抑制GM-CSF启动子的转录活性。我们的结果表明,这种体内转基因启动子活性检测系统具有细胞因子基因特异性,并且对促炎或抗炎刺激高度敏感。目前,很难在体内分析各种细胞因子的表达和相互作用。本研究建立了一个真正的体内、原位免疫组织系统,用于研究细胞因子对炎症的反应。