Warat Monika, Szliszka Ewelina, Korzonek-Szlacheta Ilona, Król Wojciech, Czuba Zenon P
Chair and Department of Microbiology and Immunology, Medical University of Silesia in Katowice, Jordana 19, 41-808 Zabrze, Poland.
Department of Toxicology and Health Protection, Toxicology and Drug Addiction Division, Medical University of Silesia in Katowice, Medyków 18, 40-752 Katowice, Poland.
Int J Mol Sci. 2014 Jun 27;15(7):11510-22. doi: 10.3390/ijms150711510.
Expression level of Tumor Necrosis Factor-related apoptosis-inducing ligand (TRAIL) receptors is one of the most important factors of TRAIL-mediated apoptosis in cancer cells. We here report for the first time data concerning TRAIL-R1 and TRAIL-R2 receptor expression on RAW264.7 macrophages. Three substances belonging to flavones: chrysin, apigenin and acacetin which differ from their substituents at the 4' position in the phenyl ring were used in assays because of the variety of biological activities (e.g., anticancer activity) of the polyphenol compounds. The expression of TRAIL-R1 and TRAIL-R2 death receptors on non-stimulated and LPS (lipopolysaccharide)-stimulated macrophages was determined using flow cytometry. We demonstrate that RAW264.7 macrophages exhibit TRAIL-R1 surface expression and that the tested compounds: chrysin, apigenin and acacetin can inhibit TRAIL-R1 death receptor expression level on macrophages.
肿瘤坏死因子相关凋亡诱导配体(TRAIL)受体的表达水平是癌细胞中TRAIL介导凋亡的最重要因素之一。我们在此首次报告有关RAW264.7巨噬细胞上TRAIL-R1和TRAIL-R2受体表达的数据。由于多酚化合物具有多种生物活性(例如抗癌活性),因此在实验中使用了三种属于黄酮类的物质:白杨素、芹菜素和刺槐素,它们在苯环的4'位上的取代基不同。使用流式细胞术测定未刺激和LPS(脂多糖)刺激的巨噬细胞上TRAIL-R1和TRAIL-R2死亡受体的表达。我们证明RAW264.7巨噬细胞表现出TRAIL-R1表面表达,并且所测试的化合物:白杨素、芹菜素和刺槐素可以抑制巨噬细胞上TRAIL-R1死亡受体的表达水平。