Dioxin induction of transgenerational inheritance of disease in zebrafish

被引:46
作者
Baker, Tracie R. [1 ]
King-Heiden, Tisha C. [2 ,3 ]
Peterson, Richard E. [1 ]
Heideman, Warren [1 ]
机构
[1] Univ Wisconsin, Sch Pharm, Div Pharmaceut Sci, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Biol, La Crosse, WI 54601 USA
[3] Univ Wisconsin, River Studies Ctr, La Crosse, WI 54601 USA
基金
美国海洋和大气管理局; 美国国家卫生研究院;
关键词
TCDD; AHR; Zebrafish; Rodent; Transgenerational; Epigenetic; AH-RECEPTOR; IN-UTERO; EPIGENETIC INHERITANCE; ENDOCRINE DISRUPTORS; LACTATIONAL EXPOSURE; DEVELOPMENTAL BASIS; PRENATAL EXPOSURE; SEX DETERMINATION; DNA METHYLATION; 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN;
D O I
10.1016/j.mce.2014.08.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dioxin (2,3,7,8-tetrachlorodibenzo-p-dioxin; TCDD) is an aryl hydrocarbon receptor (AHR) agonist, an endocrine disruptor, and a potent global pollutant. TCDD exposure is associated with diseases of almost every organ system, and its toxicity is highly conserved across vertebrates. While the acute developmental effects of dioxin exposure have been extensively studied, the ability of early sublethal exposure to produce toxicity in adulthood or subsequent generations is poorly understood. This type of question is difficult to study because of the time frame of the effects. With human subjects, such a study could span more than a lifetime. We have chosen zebrafish (Danio rerio) as a model because they are vertebrates with short generation times and consistent genetic backgrounds. Zebrafish have very modest housing needs, facilitating single and multigenerational studies with minimal time and expense. We have used this model to identify transgenerational effects of TCDD on skeletal development, sex ratio, and malemediated decreases in reproductive capacity. Here we compare these findings with transgenerational effects described in laboratory rodent species. We propose that the zebrafish is a cost-effective model system for evaluating the transgenerational effects of toxic chemicals and their role in the fetal basis of adult disease. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:36 / 41
页数:6
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