the herbicide atrazine activates endocrine gene networks via non-steroidal nr5a nuclear receptors in fish and mammalian cells除草剂阿特拉津激活内分泌基因网络通过非甾体nr5a鱼类和哺乳动物细胞的核受体.pdfVIP

the herbicide atrazine activates endocrine gene networks via non-steroidal nr5a nuclear receptors in fish and mammalian cells除草剂阿特拉津激活内分泌基因网络通过非甾体nr5a鱼类和哺乳动物细胞的核受体.pdf

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the herbicide atrazine activates endocrine gene networks via non-steroidal nr5a nuclear receptors in fish and mammalian cells除草剂阿特拉津激活内分泌基因网络通过非甾体nr5a鱼类和哺乳动物细胞的核受体

The Herbicide Atrazine Activates Endocrine Gene Networks via Non-Steroidal NR5A Nuclear Receptors in Fish and Mammalian Cells Miyuki Suzawa1,2, Holly A. Ingraham1,2* 1 Department of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, California, United States of America, 2 Department of Physiology, University of California San Francisco, San Francisco, California, United States of America Abstract Atrazine (ATR) remains a widely used broadleaf herbicide in the United States despite the fact that this s-chlorotriazine has been linked to reproductive abnormalities in fish and amphibians. Here, using zebrafish we report that environmentally relevant ATR concentrations elevated zcyp19a1 expression encoding aromatase (2.2 mg/L), and increased the ratio of female to male fish (22 mg/L). ATR selectively increased zcyp19a1, a known gene target of the nuclear receptor SF-1 (NR5A1), whereas zcyp19a2, which is estrogen responsive, remained unchanged. Remarkably, in mammalian cells ATR functions in a cell-specific manner to upregulate SF-1 targets and other genes critical for steroid synthesis and reproduction, including Cyp19A1, StAR, Cyp11A1, hCG, FSTL3, LHß, INHa, aGSU, and 11ß-HSD2. Our data appear to eliminate the possibility that ATR directly affects SF-1 DNA- or ligand-binding. Instead, we suggest that the stimulatory effects of ATR on the NR5A receptor subfamily (SF-1, LRH-1, and zff1d) are likely mediated by receptor phosphorylation, amplification of cAMP and PI3K signaling, and possibly an increase in the cAMP-responsive cellular kinase SGK-1, which is known to be upregulated in infertile women. Taken together, we propose that this pervasive and persistent environmental chemical alters hormone networks via convergence of NR5A activity

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