Hirano Toru, Higa Shinji, Arimitsu Junsuke, Naka Tetsuji, Ogata Atsushi, Shima Yoshihito, Fujimoto Minoru, Yamadori Tomoki, Ohkawara Tomoharu, Kuwabara Yusuke, Kawai Mari, Matsuda Hisashi, Yoshikawa Masayuki, Maezaki Naoyoshi, Tanaka Tetsuaki, Kawase Ichiro, Tanaka Toshio
Department of Respiratory Medicine, Allergy and Rheumatic Diseases, Osaka University Medical School, Osaka 565-0871, Japan.
Biochem Biophys Res Commun. 2006 Feb 3;340(1):1-7. doi: 10.1016/j.bbrc.2005.11.157. Epub 2005 Dec 6.
Flavonoids including luteolin, apigenin, and fisetin are inhibitors of IL-4 synthesis and CD40 ligand expression by basophils. This study was done to search for compounds with greater inhibitory activity of IL-4 expression and to clarify the molecular mechanisms through which flavonoids inhibit their expression. Of the 37 flavonoids and related compounds examined, ayanin, luteolin, and apigenin were the strongest inhibitors of IL-4 production by purified basophils in response to anti-IgE antibody plus IL-3. Luteolin did not suppress Syk or Lyn phosphorylation in basophils, nor did suppress p54/46 SAPK/JNK, p38 MAPK, and p44/42 MAPK activation by a basophilic cell line, KU812 cells, stimulated with A23187 and PMA. However, luteolin did inhibit phosphorylation of c-Jun and DNA binding activity of AP-1 in nuclear lysates from stimulated KU812 cells. These results provide a fundamental structure of flavonoids for IL-4 inhibition and demonstrate a novel action of flavonoids that suppresses the activation of AP-1.
包括木犀草素、芹菜素和漆黄素在内的类黄酮是嗜碱性粒细胞合成白细胞介素-4(IL-4)和表达CD40配体的抑制剂。本研究旨在寻找对IL-4表达具有更强抑制活性的化合物,并阐明类黄酮抑制其表达的分子机制。在所检测的37种类黄酮及相关化合物中,矢车菊素、木犀草素和芹菜素是纯化嗜碱性粒细胞在抗IgE抗体加IL-3刺激下产生IL-4的最强抑制剂。木犀草素不会抑制嗜碱性粒细胞中Syk或Lyn的磷酸化,也不会抑制嗜碱性细胞系KU812细胞在A23187和佛波酯(PMA)刺激下p54/46应激激活蛋白激酶/应激活化蛋白激酶(SAPK/JNK)、p38丝裂原活化蛋白激酶(MAPK)和p44/42 MAPK的激活。然而,木犀草素确实能抑制受刺激的KU812细胞核裂解物中c-Jun的磷酸化和活化蛋白-1(AP-1)的DNA结合活性。这些结果提供了类黄酮抑制IL-4的基本结构,并证明了类黄酮抑制AP-1激活的新作用。