Cynaropicrin, a sesquiterpene lactone, as a new strong regulator of CD29 and CD98 functions

被引:40
作者
Cho, JY [1 ]
Kim, AR
Joo, HG
Kim, BH
Rhee, MH
Yoo, ES
Katz, DR
Chain, BM
Jung, JH
机构
[1] Kangwon Natl Univ, Sch Biotechnol & Bioengn, Chunchon 200701, South Korea
[2] UCL, Sch Med, Windeyer Inst Med Sci, Dept Immunol & Mol Pathol, London W1P 6DB, England
[3] Pusan Natl Univ, Coll Pharm, Pusan 609735, South Korea
[4] Cheju Natl Univ, Dept Vet Med, Cheju 690756, South Korea
[5] Sungkyunkwan Univ, Dept Genet Engn, Suwon 440746, South Korea
[6] Kyungpook Natl Univ, Coll Vet Med, Taegu 702701, South Korea
[7] Cheju Natl Univ, Coll Med, Dept Pharmacol, Cheju 690756, South Korea
关键词
cynaropicrin; sesquiterpene lactone; homotypic aggregation; adhesion molecule; CD98; CD29 (beta 1 integrins); CD147; ERK;
D O I
10.1016/j.bbrc.2003.12.026
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
Cynaropicrin is a sesquiterpene lactone displaying immunomodulatory effects on the production of cytokine and nitric oxide from macrophages/monocytes. In this study we have examined inhibitory effect of cynaropicrin on activation of major adhesion molecules [CD29 (beta1 integrins), CD43, and CD98] on the cells assessed by U937 (promonocytic cells) homotypic aggregation. Cynaropicrin potently blocked CD29 (beta1 integrins)- and CD98-induced homotypic aggregation with IC(50) values of 3.46 and 2.98 muM, respectively, without displaying cytotoxicity. Similarly, flow cytometric analysis exhibited that cynaropicrin down-regulated strikingly surface level of CD29 and CD147, a functional regulator of CD98, but not CD43. More importantly, cynaropicrin inhibition was linked to blockade of extracellular signal-related kinase (ERK) activation and distinct from other enzyme inhibitors including rottlerin, propranolol, forskolin, and chloroquine, but not cytochalasin B. Therefore, our finding is the first demonstration that cynaropicrin may be a potent functional regulator of CD29 and CD98 via interrupting ERK activation which may be linked to cytoskeleton rearrangement, suggesting further application to CD29- and CD98-mediated diseases such as virus-induced chronic inflammation, and invasion, migration, and metastasis of leukocyte cancer cells. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:954 / 961
页数:8
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