Polychlorinated bipbenyls suppress thyroid hormone-induced transactivation

被引:108
作者
Iwasaki, T
Miyazaki, W
Takeshita, A
Kuroda, Y
Koibuchia, N [1 ]
机构
[1] Gunma Univ, Sch Med, Dept Physiol, Maebashi, Gumma 3718511, Japan
[2] Japan Sci & Technol Corp, CREST, Kawaguchi, Saitama 3320012, Japan
[3] Tottori Univ, Fac Med, Dept Immunol, Sch Life Sci, Yonago, Tottori 6838503, Japan
[4] Okinaka Mem Inst Med Res, Div Endocrinol & Metab, Tokyo 1058470, Japan
[5] Tokyo Metropolitan Inst Neurosci, Dept Mol & Cellular Neurobiol, Tokyo 1838526, Japan
关键词
PCB; hydroxylated PCB; thyroid hormone receptor; SRC-1; brain;
D O I
10.1016/S0006-291X(02)02659-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polychlorinated biphenyls (PCBs) have been known as environmental endocrine disrupting chemical that causes various abnormalities in many organs including the central nervous system (CNS). To examine the effect of PCBs on thyroid hormone (T3)-mediated transcription, transfection-based reporter assays were performed. Surprisingly, as low as 10(-10) M of 4(OH)-2',3,3',4', 5'-pentachloro biphenyl suppressed T3-induced transactivation by thyroid hormone receptor (TR) in various cell lines. Interestingly, among the cell lines that we tested, brain-derived cell line TE671 cells showed strong suppression by the PCB. The suppression of TR action by the PCB was not likely due to the ligand competition with T3. Various compounds of PCBs showed similar suppression. However, PCBs did not suppress glucocorticoid receptor-mediated transcription. Finally, we showed that PCBs suppress TR/coactivator (SRC-1) complex-mediated transactivation. In summary, our results suggest that very low dose of PCBs can potentially interfere with TR-mediated transactivation by influencing on TR/coactivator complex. As such, PCBs may disturb growth and development of TH target organ, particularly in the CNS. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:384 / 388
页数:5
相关论文
共 28 条
[21]   EFFECTS OF THYROID DYSFUNCTION ON DEVELOPMENT OF RAT CEREBELLUM, WITH SPECIAL REFERENCE TO CELL-DEATH WITHIN INTERNAL GRANULAR LAYER [J].
RABIE, A ;
FAVRE, C ;
CLAVEL, MC ;
LEGRAND, J .
BRAIN RESEARCH, 1977, 120 (03) :521-531
[22]   Analysis of hydroxylated metabolites of PCBs (OH-PCBs) and other chlorinated phenolic compounds in whole blood from Canadian Inuit [J].
Sandau, CD ;
Ayotte, P ;
Dewailly, E ;
Duffe, J ;
Norstrom, RJ .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2000, 108 (07) :611-616
[23]   Pentachlorophenol and hydroxylated polychlorinated biphenyl metabolites in umbilical cord plasma of neonates from coastal populations in Quebec [J].
Sandau, CD ;
Ayotte, P ;
Dewailly, É ;
Duffe, J ;
Norstrom, RJ .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2002, 110 (04) :411-417
[24]  
SCHMIDT JV, 1993, J BIOL CHEM, V268, P22203
[25]   Thyroid hormone response elements differentially modulate the interactions of thyroid hormone receptors with two receptor binding domains in the steroid receptor coactivator-1 [J].
Takeshita, A ;
Yen, PM ;
Ikeda, M ;
Cardona, GR ;
Liu, Y ;
Koibuchi, N ;
Norwitz, ER ;
Chin, WW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (34) :21554-21562
[26]   POLYCHLORINATED-BIPHENYLS AND THE DEVELOPING NERVOUS-SYSTEM - CROSS-SPECIES COMPARISONS [J].
TILSON, HA ;
JACOBSON, JL ;
ROGAN, WJ .
NEUROTOXICOLOGY AND TERATOLOGY, 1990, 12 (03) :239-248
[27]   Physiological and molecular basis of thyroid hormone action [J].
Yen, PM .
PHYSIOLOGICAL REVIEWS, 2001, 81 (03) :1097-1142
[28]   The mechanism of action of thyroid hormones [J].
Zhang, JS ;
Lazar, MA .
ANNUAL REVIEW OF PHYSIOLOGY, 2000, 62 :439-466