Epigallocatechin gallate inhibits histamine release from rat basophilic leukemia (RBL-2H3) cells: Role of tyrosine phosphorylation pathway

被引:48
|
作者
Yamashita, K
Suzuki, Y
Matsui, T
Yoshimaru, T
Yamaki, M
Suzuki-Karasaki, M
Hayakawa, S
Shimizu, K
机构
[1] Nihon Univ, Sch Med, Dept Immunol & Microbiol, Itabashi Ku, Tokyo 1738610, Japan
[2] Nihon Univ, Sch Med, Dept Gynecol & Obstet, Tokyo 1738610, Japan
[3] Hitachi Chem Co Ltd, Pharmaceut Res Lab, Hitachi, Ibaraki 3178555, Japan
关键词
D O I
10.1006/bbrc.2000.3200
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
Some tea polyphenolic compounds including (-)epigallocatechin gallate (EGCG) have been shown, to inhibit histamine release from mast cells through poorly understood mechanisms. By using a mast cell model rat basophilic leukemia (RBL-2H3) cells we explored the mechanism of the inhibition. EGCG inhibited histamine release from RBL-2H3 cells in response to antigen or the calcium-ionophore A23187, while (-)epicatechin (EC) had little effect, Increased tyrosine phosphorylation of several proteins including similar to 120 kDa proteins occurred in parallel with the secretion induced by either stimulation. EGCG; also inhibited tyrosine phosphorylation of the similar to 120-kDa proteins induced by either stimulation, whereas EC did not. The tyrosine kinase-specific inhibitor piceatannol inhibited the secretion and tyrosine phosphorylation of these proteins induced by either stimulation also. Further analysis showed that the focal adhesion kinase pp125(FAK) was one of the similar to 120-kDa proteins. These findings suggest that EGCG; prevents histamine release from mast cells mainly by inhibiting tyrosine phosphorylation of proteins including pp125FAK (C) 2000 Academic Press.
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收藏
页码:603 / 608
页数:6
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