Abscisic Acid Released by Human Monocytes Activates Monocytes and Vascular Smooth Muscle Cell Responses Involved in Atherogenesis

被引:76
作者
Magnone, Mirko [1 ]
Bruzzone, Santina [1 ,2 ]
Guida, Lucrezia [1 ]
Damonte, Gianluca [1 ]
Millo, Enrico [1 ]
Scarft, Sonia [1 ,2 ]
Usai, Cesare [3 ]
Sturla, Laura [1 ]
Palombo, Domenico [4 ]
De Flora, Antonio [1 ]
Zocchi, Elena [1 ,2 ]
机构
[1] Univ Genoa, Biochem Sect, Dept Expt Med, I-16132 Genoa, Italy
[2] Adv Biotechnol Ctr, I-16132 Genoa, Italy
[3] CNR, Inst Biophys, I-16149 Genoa, Italy
[4] San Martino Hosp, Vasc & Endovasc Surg Unit, I-16132 Genoa, Italy
关键词
CYCLIC-ADP-RIBOSE; CHEMOATTRACTANT PROTEIN-1 GENE; NF-KAPPA-B; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; C-DEPENDENT PROCESSES; POLYMORPHONUCLEAR NEUTROPHILS; HUMAN GRANULOCYTES; EXPRESSION; ATHEROSCLEROSIS; PROLIFERATION;
D O I
10.1074/jbc.M809546200
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
Abscisic acid (ABA) is a phytohormone recently identified as a new endogenous pro-inflammatory hormone in human granulocytes. Here we report the functional activation of human monocytes and vascular smooth muscle cells by ABA. Incubation of monocytes with ABA evokes an intracellular Ca2+ rise through the second messenger cyclic ADP-ribose, leading to NF-kappa B activation and consequent increase of cyclooxygenase-2 expression and prostaglandin E-2 production and enhanced release of MCP-1 (monocyte chemoattractant protein-1) and of metalloprotease-9, all events reportedly involved in atherogenesis. Moreover, monocytes release ABA when exposed to thrombin-activated platelets, a condition occurring at the injured vascular endothelium; monocyte-derived ABA behaves as an autocrine and paracrine pro-inflammatory hormone-stimulating monocyte migration and MCP-1 release, as well as vascular smooth muscle cells migration and proliferation. These results, and the presence of ABA in human arterial plaques at a 10-fold higher concentration compared with normal arterial tissue, identify ABA as a new signal molecule involved in the development of atherosclerosis and suggest a possible new target for anti-atherosclerotic therapy.
引用
收藏
页码:17808 / 17818
页数:11
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