Takahashi Suzuka, Yamamoto Chika, Kaji Toshiyuki
Faculty of Pharmaceutical Sciences, Tokyo University of Science.
Yakugaku Zasshi. 2014;134(7):805-7. doi: 10.1248/yakushi.14-00017-6.
Blood vessels are composed of endothelial cells and other cell types and they are ubiquitously present in every organ. It is important to study the toxicity of cadmium to endothelial cells for understanding organic cadmium toxicity. Although vascular toxicity of cadmium has been studied previously, little is known about the underlying toxicity mechanism. Cadmium-sensitive mice have been reported to show high expression of zinc transporter, ZIP8, in endothelial cells of the testis vasculature, which produces genetic difference in the response to the testicular cadmium toxicity. ZIP8 is involved in the transport of zinc, manganese, and cadmium from the extracellular space or intracellular compartments into the cytosol. In this report, we have described how cadmium is one of the inducers of ZIP8 expression in vascular endothelial cells, and that cadmium cytotoxicity partly depends on the ZIP8 expression levels.
血管由内皮细胞和其他细胞类型组成,遍布于每个器官。研究镉对内皮细胞的毒性对于理解有机镉毒性很重要。尽管此前已对镉的血管毒性进行了研究,但对其潜在的毒性机制知之甚少。据报道,镉敏感小鼠的睾丸脉管系统内皮细胞中锌转运体ZIP8表达较高,这在对睾丸镉毒性的反应中产生了遗传差异。ZIP8参与锌、锰和镉从细胞外空间或细胞内区室转运到细胞质中。在本报告中,我们描述了镉是血管内皮细胞中ZIP8表达的诱导剂之一,并且镉的细胞毒性部分取决于ZIP8的表达水平。