4.0 Article

Endocrine disruption effects of 2,2′,4,4′,6-pentabromodiphenylether (BDE100) in reporter gene assays

期刊

JOURNAL OF ENVIRONMENTAL MONITORING
卷 13, 期 4, 页码 850-854

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0em00654h

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资金

  1. National Natural Science [20977047]
  2. Science & Technology Ministry of China [2008ZX08526-003]
  3. Specialized Research Fund for the Doctoral Program of Higher Education [200802841030]
  4. Talent Introduction and Cultivation Foundation of Nanjing University
  5. Canada Research Chair program
  6. State Key Laboratory in Marine Pollution, City University of Hong Kong
  7. King Saud University

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Polybrominated diphenyl ethers (PBDEs) constitute an important group of flame retardants. 2,20,4,40,6-Pentabromodiphenylether (BDE100) is a prominent PBDE congener in some human populations. The potential of BDE100 to modulate responses mediated by the estrogen (ER), thyroid hormone (ThR) or androgen receptors (AR) were investigated by use of transactivation reporter gene assays. The African green monkey kidney CV-1 cell transiently transfected with the constructed reporter gene plasmid ERE-TATA-Luc and pUAS-tk-Luc with luciferase (Luc) under control of the estrogen response (ERE), or thyroid hormone response (ThRE) elements were used to evaluate (anti) estrogen and thyroid effects of BDE100. The (anti) androgenic potency of BDE100 was also evaluated by use of MDA-kb2 cells, which were stably transfected with MMTV-luciferase. The assays displayed appropriate responses to known natural estrogen 17 beta-estradiol (E2), ThR ligand triiodothyronine (T3), and the AR agonist 5 alpha-dihydrotestosterone (DHT). 10 or 50 mu M BDE100 significantly up-regulated expression of Luc under control of the ER. Antiestrogenic potency was observed for BDE100 (IC50 6.21 mu M). Co-exposure to 50 mu M BDE100 significantly enhanced expression of Luc caused by 5 nM T3. BDE100 was antiandrogenic at 10 and 50 mu M with an IC50 of 28.60 mu M BDE100. These results suggest that BDE100 can modulate the endocrine system in multiple ways by interfering with several hormonal signaling pathways simultaneously.

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