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. Key Words: atherosclerosis Ⅲ cigarette smoking Ⅲ endothelial Ⅲ metals Ⅲ microarray Ⅲ osteoporosis C igarette smoking is a well-established risk factor for cardiovascular diseases. We have previously shown that among young males, smoking was the most important risk factor for early pro-atherogenic vessel wall changes (increased intima-media thickness). 1 However, the mechanisms by which cigarette smoke constituents contribute to atherogenesis are poorly understood. Therefore, we performed a number of in vitro analyses and could show that out of 4800 different compounds in cigarette smoke, the mixture of metals and oxidants constitutes the crucial endotheliumdamaging noxa. 2 This combination leads to a chain reaction of protein oxidation, functional impairment of the microtubule system, contraction of endothelial cells, endothelial dysfunction, and, finally, to denudation of the inner vascular surface. 2 According to the "response to injury" hypothesis of atherosclerosis, endothelial dysfunction and vessel denudation play the central role in the atherogenic process. 3 Cigarette smoke contains a number of different metals, including aluminum (Al), cadmium, chromium (Cr), copper (Cu), lead (Pb), mercury (Hg), nickel (Ni), and zinc (Zn). 4 Smoking leads to an increase of serum Cd, Cr, and Pb, 5 and increased serum Cd levels have been shown to contribute to smoking-induced peripheral arterial disease. 6 Abu-Hayyeh et al (2001) reported that along with increased serum levels, Cd also accumulates in the aortic vessel walls of smokers at concentrations of up to 7 mol/L. 7 Furthermo...