6-Methylsulfinylhexyl isothiocyanate modulates endothelial cell function and suppresses leukocyte adhesion

被引:14
|
作者
Okamoto, Takayuki [1 ]
Akita, Nobuyuki [2 ]
Nagai, Masashi [3 ]
Hayashi, Tatsuya [4 ]
Suzuki, Koji [5 ]
机构
[1] Mie Univ, Dept Mol Pathobiol & Cell Adhes Biol, Grad Sch Med, Tsu, Mie 5148507, Japan
[2] Suzuka Univ Med Sci, Fac Med Engn, Suzuka, Mie 5100293, Japan
[3] Kinjirushi Co Ltd, Nakagawa Ku, Nagoya, Aichi 4548526, Japan
[4] Mie Prefecture Coll Nursing, Dept Biochem, Tsu, Mie 5140116, Japan
[5] Suzuka Univ Med Sci, Fac Pharmaceut Sci, Suzuka, Mie 5138679, Japan
基金
日本学术振兴会;
关键词
6-Methylsulfinylhexyl isothiocyanate; Endothelial cells; Blood coagulation; Inflammation; Leukocyte adhesion; ACTIVATED PROTEIN-C; TISSUE FACTOR EXPRESSION; FACTOR-KAPPA-B; 6-(METHYLSULFINYL)HEXYL ISOTHIOCYANATE; ALPHA PRODUCTION; WASABI; COAGULATION; MACROPHAGES; PATHWAY; ANTIPLATELET;
D O I
10.1007/s11418-013-0784-x
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
6-Methylsulfinylhexyl isothiocyanate (6-MSITC) is an active compound in wasabi (Wasabia japonica Matsum.), which is one of the most popular spices in Japan. 6-MSITC suppresses lipopolysaccharide-induced macrophage activation, arachidonic- or adenosine diphosphate-induced platelet activation, and tumor cell proliferation. These data indicate that 6-MSITC has several biological activities involving anti-inflammatory, anti-coagulant, and anti-apoptosis properties. Endothelial cells (ECs) maintain vascular homeostasis and play crucial roles in crosstalk between blood coagulation and vascular inflammation. In this study, we determined the anti-coagulant and anti-inflammatory effects of 6-MSITC on human umbilical vein endothelial cells (HUVECs). 6-MSITC slightly reduced tissue factor expression, but did not alter von Willebrand factor release in activated HUVECs. 6-MSITC modulated the generation of activated protein C, which is essential for negative regulation of blood coagulation, on normal ECs. In addition, 6-MSITC reduced tumor necrosis factor-alpha (TNF-alpha)-induced interleukin-6 and monocyte chemoattractant protein-1 expression. 6-MSITC markedly attenuated TNF-alpha-induced adhesion of human monoblast U937 cells to HUVECs and reduced vascular cell adhesion molecule-1 and E-selectin mRNA expression in activated ECs. These results showed that 6-MSITC modulates EC function and suppresses cell adhesion. This study provides new insight into the mechanism of the anti-inflammatory effect of 6-MSITC, suggesting that 6-MSITC has therapeutic potential as a treatment for vasculitis and vascular inflammation.
引用
收藏
页码:144 / 153
页数:10
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