(-)-epicatechin gallate accumulates in foamy macrophages in human atherosclerotic aorta: Implication in the anti-atherosclerotic actions of tea catechins

被引:58
作者
Kawai, Yoshichika [1 ]
Tanaka, Hiroko [1 ]
Murota, Kaeko [1 ]
Naito, Michitaka [2 ]
Terao, Junji [1 ]
机构
[1] Univ Tokushima, Grad Sch Nutr & Biosci, Dept Food Sci, Tokushima 7708503, Japan
[2] Sugiyama Jogakuen Univ, Sch & Grad Sch Life Studies, Div Nutr & Hlth, Nagoya, Aichi 4648662, Japan
基金
日本科学技术振兴机构;
关键词
tea catechin; monoclonal antibody; atherosclerosis; macrophage; oxidative stress; scavenger receptor;
D O I
10.1016/j.bbrc.2008.07.086
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 localization and target sites of tea catechins underlying their biological activity including anti-atherosclerotic activity have not yet been fully understood. To identify the target sites of catechins in vivo, we have developed a novel monoclonal antibody (mAb5A3) specific for (-)-epicatechin-3-gallate (ECg), one of the major tea catechins. The immunoreactive materials with mAb5A3 were detected in the human atherosclerotic lesions but not in the normal aorta, and were specifically localized in the macrophage-derived foam cells. fit vitro experiments using macrophage-like cell lines also showed the significant accumulation of ECg in the cells. We also demonstrated that ECg could suppress the gene expression of a scavenger receptor CD36, a key molecule for foam cell formation, in macrophage cells. These results, for the first time, showed the target site of a tea component ECg in the aorta and might provide a mechanism for the anti-atherosclerotic actions of the catechins. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:527 / 532
页数:6
相关论文
共 18 条
[1]   In vivo comparison of the bioavailability of (+)-catechin, (-)-epicatechin and their mixture in orally administered rats [J].
Baba, S ;
Osakabe, N ;
Natsume, M ;
Muto, Y ;
Takizawa, T ;
Terao, J .
JOURNAL OF NUTRITION, 2001, 131 (11) :2885-2891
[2]   Antioxidant activity of tea polyphenols in vivo: Evidence from animal studies [J].
Frei, B ;
Higdon, JV .
JOURNAL OF NUTRITION, 2003, 133 (10) :3275S-3284S
[3]   GREEN TEA COMPOSITION, CONSUMPTION, AND POLYPHENOL CHEMISTRY [J].
GRAHAM, HN .
PREVENTIVE MEDICINE, 1992, 21 (03) :334-350
[4]   Endogenous formation of novel halogenated 2′-deoxycytidine -: Hypohalous acid-mediated DNA modification at the site of inflammation [J].
Kawai, Y ;
Morinaga, H ;
Kondo, H ;
Miyoshi, N ;
Nakamura, Y ;
Uchida, K ;
Osawa, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (49) :51241-51249
[5]   Immunohistochemical detection of a substituted 1,N2-ethenodeoxyguanosine adduct by ω-6 polyunsaturated fatty acid hydroperoxides in the liver of rats fed a choline-deficient, L-amino acid-defined diet [J].
Kawai, Y ;
Kato, Y ;
Nakae, D ;
Kusuoka, O ;
Konishi, Y ;
Uchida, K ;
Osawa, T .
CARCINOGENESIS, 2002, 23 (03) :485-489
[6]  
KAWAI Y, ARCH BIOCH IN PRESS
[7]   Macrophage as a target of quercetin glucuronides in human atherosclerotic arteries - Implication in the anti-atherosclerotic mechanism of dietary flavonoids [J].
Kawai, Yoshichika ;
Nishikawa, Tomomi ;
Shiba, Yuko ;
Saito, Satomi ;
Murota, Kaeko ;
Shibata, Noriyuki ;
Kobayashi, Makio ;
Kanayama, Masaya ;
Uchida, Koji ;
Terao, Junji .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (14) :9424-9434
[8]  
McKay DL, 2002, J AM COLL NUTR, V21, P1
[9]  
Meng XF, 2001, DRUG METAB DISPOS, V29, P789
[10]   Tea catechins prevent the development of atherosclerosis in apoprotein E-deficient mice [J].
Miura, Y ;
Chiba, T ;
Tomita, I ;
Koizumi, H ;
Miura, S ;
Umegaki, K ;
Hara, Y ;
Ikeda, M ;
Tomita, T .
JOURNAL OF NUTRITION, 2001, 131 (01) :27-32