Increased serum cadmium and strontium levels in young smokers - Effects on arterial endothelial cell gene transcription

被引:71
作者
Bernhard, D
Rossmann, A
Henderson, B
Kind, M
Seubert, A
Wick, G
机构
[1] Innsbruck Med Univ, Vasc Biol Grp, Div Expt Pathophysiol & Immunol, Bioctr, A-6020 Innsbruck, Austria
[2] Univ Marburg, Dept Chem, Marburg, Germany
关键词
atherosclerosis; cigarette smoking; endothelial; metals; microarray; osteoporosis;
D O I
10.1161/01.ATV.0000205616.70614.e5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-Metal constituents of tobacco have long been suspected to contribute to cardiovascular diseases. In this study, we determined the serum concentrations of aluminum, cadmium (Cd), cobalt, copper, iron, manganese, nickel, lead, strontium (Sr), and zinc of young nonsmokers, passive smokers, and smokers. Methods and Results-Cd and Sr were found to be significantly increased in smokers compared with nonsmokers. The effects of these metals on primary arterial endothelial cells were then assessed using microarray technology and real-time polymerase chain reaction (RT-PCR). The data showed that Sr does not interfere with endothelial cell transcription. In contrast, the effects of Cd in amounts delivered to the human body by smoking were dramatic. Conclusions-Arterial endothelial cells responded to Cd exposure by massively upregulating metal and oxidant defense genes (metallothioneins) and by downregulating a number of transcription factors. In addition, the mRNA of the intermediate filament protein vimentin, crucial for the maintenance of cellular shape, was reduced. Surprisingly, a number of pro-inflammatory genes were downregulated in response to Cd. The present data suggest that by delivering Cd to the human body, smoking deregulates transcription, exerts stress, and damages the structure of the vascular endothelium; furthermore, in contrast to the effects of cigarette smoke as a whole, Cd seems to possess antiinflammatory properties.
引用
收藏
页码:833 / 838
页数:6
相关论文
共 30 条
[1]   Cadmium accumulation in aortas of smokers [J].
Abu-Hayyeh, S ;
Sian, M ;
Jones, KG ;
Manuel, A ;
Powell, JT .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (05) :863-867
[2]   Rotation between markers of systemic vascular inflammation and smoking in women [J].
Bermudez, EA ;
Rifai, N ;
Buring, JE ;
Manson, JE ;
Ridker, PM .
AMERICAN JOURNAL OF CARDIOLOGY, 2002, 89 (09) :1117-+
[3]   Apoptosis induced by the histone deacetylase inhibitor sodium butyrate in human leukemic lymphoblasts [J].
Bernhard, D ;
Ausserlechner, MJ ;
Tonko, M ;
Löffler, M ;
Hartmann, BL ;
Csordas, A ;
Kofler, R .
FASEB JOURNAL, 1999, 13 (14) :1991-2001
[4]   Metals in cigarette smoke [J].
Bernhard, D ;
Rossmann, A ;
Wick, G .
IUBMB LIFE, 2005, 57 (12) :805-809
[5]   Cigarette smoke metal-catalyzed protein oxidation leads to vascular endothelial cell contraction by depolymerization of microtubules [J].
Bernhard, D ;
Csordas, A ;
Henderson, B ;
Rossmann, A ;
Kind, M ;
Wick, G .
FASEB JOURNAL, 2005, 19 (09) :1096-1107
[6]   Disruption of vascular endothelial homeostasis by tobacco smoke - impact on atherosclerosis [J].
Bernhard, D ;
Pfister, G ;
Huck, CW ;
Kind, M ;
Salvenmoser, W ;
Bonn, GK ;
Wick, G .
FASEB JOURNAL, 2003, 17 (13) :2302-+
[7]  
Bernhard David, 2004, Journal of Pharmacological and Toxicological Methods, V50, P45, DOI 10.1016/j.vascn.2004.01.003
[8]   Annexin 1-deficient neutrophils exhibit enhanced transmigration in vivo and increased responsiveness in vitro [J].
Chatterjee, BE ;
Yona, S ;
Rosignoli, G ;
Young, RE ;
Nourshargh, S ;
Flower, RJ ;
Perretti, M .
JOURNAL OF LEUKOCYTE BIOLOGY, 2005, 78 (03) :639-646
[9]  
Dai Jie, 2003, Cancer Immun, V3, P1
[10]   Kruppel-like factors 4 and 5: the yin and yang regulators of cellular proliferation [J].
Ghaleb, AM ;
Nandan, MO ;
Chanchevalap, S ;
Dalton, WB ;
Hisamuddin, IM ;
Yang, VW .
CELL RESEARCH, 2005, 15 (02) :92-96