Understanding dioxin developmental toxicity using the zebrafish model

Authors

  • Sara A. Carney,

    1. Molecular and Environmental Toxicology Center, University of Wisconsin, Madison, Wisconsin
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    • Sara A. Carney and Amy L. Prasch contributed equally to this publication.

  • Amy L. Prasch,

    1. Molecular and Environmental Toxicology Center, University of Wisconsin, Madison, Wisconsin
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    • Sara A. Carney and Amy L. Prasch contributed equally to this publication.

  • Warren Heideman,

    1. Molecular and Environmental Toxicology Center, University of Wisconsin, Madison, Wisconsin
    2. School of Pharmacy, University of Wisconsin, Madison, Wisconsin
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  • Richard E. Peterson

    Corresponding author
    1. Molecular and Environmental Toxicology Center, University of Wisconsin, Madison, Wisconsin
    2. School of Pharmacy, University of Wisconsin, Madison, Wisconsin
    • School of Pharmacy, University of Wisconsin, 777 Highland Ave., Madison, WI 53705-2222
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Abstract

Zebrafish (Danio rerio) have advantages over mammals as an animal model for investigating developmental toxicity. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (dioxin, TCDD), a persistent global contaminant, is the most comprehensively studied developmental toxicant in zebrafish. The hallmark responses of TCDD developmental toxicity manifested in zebrafish larvae include edema, anemia, hemorrhage, and ischemia associated with arrested growth and development. Heart and vasculature development and function are severely impaired, and jaw malformations occur secondary to inhibited chondrogenesis. The swim bladder fails to inflate, and the switch from embryonic to adult erythropoiesis is blocked. This profile of developmental toxicity responses, commonly referred to as “blue sac syndrome” because the edematous yolk sac appears blue, is observed in the larval form of all freshwater fish species exposed to TCDD at the embryonic stage of development. Components of the aryl hydrocarbon receptor/aryl hydrocarbon receptor nuclear translocator (AHR/ARNT) signaling pathway in zebrafish have been identified and functionally characterized. Their role in mediating TCDD toxicity has been determined using morpholinos to specifically knockdown the translation of zfAHR1, zfAHR2, zfARNT1, and zfARNT2 mRNAs, respectively, and a line of zfARNT2 null mutant zebrafish has provided further insight. These studies have shown that zfAHR2 and zfARNT1 mediate TCDD developmental toxicity. In addition, the growing use of molecular and genomic tools for research on zebrafish have led to advances in our understanding of the mechanism of TCDD developmental toxicity at the molecular level, including the recent finding that toxicity is not mediated by increased cytochrome P4501A (zfCYP1A) expression. Birth Defects Research (Part A), 2005. © 2005 Wiley-Liss, Inc.

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