Flavonoids differentially regulate IFNγ-induced ICAM-1 expression in human keratinocytes:: molecular mechanisms of action

被引:50
作者
Bito, T [1 ]
Roy, S
Sen, CK
Shirakawa, T
Gotoh, A
Ueda, M
Ichihashi, M
Packer, L
机构
[1] Univ Calif Berkeley, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
[2] Ohio State Univ, Med Ctr, Mol Med Lab, Davis Heart & Lung Res Inst, Columbus, OH 43210 USA
[3] Kobe Univ, Grad Sch Med, Dept Urol, Chuo Ku, Kobe, Hyogo 6500017, Japan
[4] Kobe Univ, Grad Sch Med, Dept Dermatol, Chuo Ku, Kobe, Hyogo 6500017, Japan
[5] Univ So Calif, Sch Pharm, Dept Mol Pharmacol & Toxicol, Los Angeles, CA 90089 USA
关键词
cell adhesion; taxifolin; tyrosine kinase activation; signal transducers and activators of transcription 1;
D O I
10.1016/S0014-5793(02)02810-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effect of plant flavonoids on intercellular adhesion molecule-1 (ICAM-1) expression in human keratinocyte was investigated. ICAM-1 is known to mediate skin inflammation. Among the flavonoids tested, taxifolin was the most potent in inhibiting interferon gamma (IFNgamma)-induced ICAM-1 protein as well as mRNA expression in human keratinocytes. Much smaller dosages of taxifolin were required in primary keratinocytes compared to HaCaT (immortalized cell) to achieve similar levels of inhibition in the inducible ICAM-1 expression. Regulation of inducible ICAM-1 expression by taxifolin was at transcriptional level by inhibiting the activation of signa transducers and activators of transcription (STAT)1 and protein tyrosine phosphorylation of Janus kinase (JAK)1 suggesting that the JAK-STAT pathway may be the molecular site of action of taxifolin. Finally, taxifolin pre-treatment also potently inhibited IFNgamma-induced ICAM-1 expression in a reconstructed human skin equivalent suggesting therapeutic potential of taxifolin in skin pathological conditions related to increased cell adhesion and inflammation. (C) 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:145 / 152
页数:8
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