Multiple roles of cadmium in cell death and survival

被引:347
作者
Templeton, Douglas M. [1 ]
Liu, Ying [1 ]
机构
[1] Univ Toronto, Lab Med & Pathobiol, Toronto, ON M5S 1A8, Canada
基金
加拿大健康研究院;
关键词
Cadmium; Carcinogenesis; Apoptosis; Autophagy; Mesangial cell; Kinase activation; ACTIVATED PROTEIN-KINASE; INDUCED MALIGNANT-TRANSFORMATION; C-FOS; DNA-DAMAGE; IN-VITRO; OXIDATIVE STRESS; HEAVY-METALS; ENVIRONMENTAL EXPOSURE; OCCUPATIONAL-EXPOSURE; DEPENDENT APOPTOSIS;
D O I
10.1016/j.cbi.2010.03.040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Cadmium is a toxic metal with no known biological function. It is increasingly important as an environmental hazard to both humans and wildlife, and it exemplifies the double edged nature of many toxic substances. Thus, on the one hand cadmium can act as a mitogen, stimulate cell proliferation, inhibit apoptosis, inhibit DNA repair, and promote cancer in a number of tissues. On the other hand, it causes tissue damage, notably in the kidney, by inducing cell death. At low and moderate concentrations in cell culture systems (e.g., 0.1-10 mu M) cadmium primarily causes apoptosis, and at higher concentrations (>50 mu M) necrosis becomes evident. This generalization appears to hold in vivo. There is also evidence of cadmium-induced autophagy, although whether this is a direct cause of cell death remains uncertain. After discussing these generalities, this review considers the details of apoptotic death, and its inhibition, in renal mesangial cells. We also present evidence for the effect of environmental exposure to cadmium in affecting renal function, and in particular review the evidence for the role of the mesangial cell in cadmium nephrotoxicity. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:267 / 275
页数:9
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