Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on preimplantation mouse embryos

被引:29
作者
Wu, Q
Ohsako, S
Baba, T
Miyamoto, K
Tohyama, C
机构
[1] Natl Inst Environm Studies, Environm Hlth Sci Div, Tsukuba, Ibaraki 3058506, Japan
[2] Univ Tsukuba, Inst Appl Biochem, Tsukuba, Ibaraki 3058572, Japan
[3] JST, CREST, Kawaguchi 3320012, Japan
基金
日本科学技术振兴机构;
关键词
preimplantation embryo; TCDD; AhR; Arnt; CYP1A1; dose-dependent; apoptosis;
D O I
10.1016/S0300-483X(02)00047-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is a potent environmental contaminant that can exert developmental toxicity. To investigate the stage-specific effects of TODD on preimplantation embryos, we exposed mouse embryos to TODD at different stages (1-, 2-, and 8-cell) and collected them at different stages of development (the 1- or 2-, 8-cell, and blastocyst stage, respectively). Semiquantitative RT-PCR revealed increased constitutive gene expression of the arylhydrocarbon receptor (AhR) and AhR nuclear translocator (Arnt) at the 1-cell stage, decreased expression at the 2- to 8-cell stage, and increased expression again at the blastocyst stage, and addition of TODD to media did not affect their mRNA levels. Interestingly, no cytochrome P4501A1 (CYP1A1) mRNA was detected in embryos at the 1-, 2-, and 8-cell stages after exposure to 10 nM TCDD for 12 or 24 h, whereas CYP1A1 mRNA was significantly increased at the blastocyst stage in response to TCDD, and its induction was found to be concentration-dependent on TCDD exposure from 0.01 to 10 nM for 24 h. In addition, no significant differences in development rate of preimplantation embryos, cell number of blastocyst embryos, or apoptotic indices, such as TUNEL-positive cell number or Bax/Bcl-2 expression ratios were observed at the blastocyst stage between TCDD-exposed groups and non-exposed group. These results suggest that the sensitivity to TCDD differs with the embryonic stage, which may reflect an ability of embryos to adapt to environmental stressors, such as dioxins. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:119 / 129
页数:11
相关论文
共 27 条
[1]   RT-PCR quantification of AHR, ARNT, GR, and CYP1A1 mRNA in craniofacial tissues of embryonic mice exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin and hydrocortisone [J].
Abbott, BD ;
Schmid, JE ;
Brown, JG ;
Wood, CR ;
White, RD ;
Buckalew, AR ;
Held, GA .
TOXICOLOGICAL SCIENCES, 1999, 47 (01) :76-85
[2]   2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN (TCDD) ACCELERATES DIFFERENTIATION OF MURINE PREIMPLANTATION EMBRYOS INVITRO [J].
BLANKENSHIP, AL ;
SUFFIA, MC ;
MATSUMURA, F ;
WALSH, KJ ;
WILEY, LM .
REPRODUCTIVE TOXICOLOGY, 1993, 7 (03) :255-261
[3]  
Bryant PL, 1997, TERATOLOGY, V55, P326
[4]   A CRITICAL-REVIEW OF THE DEVELOPMENTAL TOXICITY AND TERATOGENICITY OF 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN - RECENT ADVANCES TOWARD UNDERSTANDING THE MECHANISM [J].
COUTURE, LA ;
ABBOTT, BD ;
BIRNBAUM, LS .
TERATOLOGY, 1990, 42 (06) :619-627
[5]   Markedly increased constitutive CYP1A1 mRNA levels in the fertilized ovum of the mouse [J].
Dey, A ;
Nebert, DW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 251 (02) :657-661
[6]   Expression of caspase and BCL-2 apoptotic family members in mouse preimplantation embryos [J].
Exley, GE ;
Tang, CY ;
McElhinny, AS ;
Warner, CM .
BIOLOGY OF REPRODUCTION, 1999, 61 (01) :231-239
[7]   THE TRANSITION FROM MATERNAL TO EMBRYONIC CONTROL IN THE 2-CELL MOUSE EMBRYO [J].
FLACH, G ;
JOHNSON, MH ;
BRAUDE, PR ;
TAYLOR, RAS ;
BOLTON, VN .
EMBO JOURNAL, 1982, 1 (06) :681-686
[8]   EFFECTS OF 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN ADMINISTERED TO PREGNANT RATS DURING THE PRE-IMPLANTATION PERIOD [J].
GIAVINI, E ;
PRATI, M ;
VISMARA, C .
ENVIRONMENTAL RESEARCH, 1982, 29 (01) :185-189
[9]   A RAPID PROCEDURE FOR VISUALIZING THE INNER CELL MASS AND TROPHECTODERM NUCLEI OF MOUSE BLASTOCYSTS INSITU USING POLYNUCLEOTIDE-SPECIFIC FLUOROCHROMES [J].
HANDYSIDE, AH ;
HUNTER, S .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1984, 231 (03) :429-434
[10]   Effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin on the expression of cytochrome P450 1A1, the aryl hydrocarbon receptor, and the aryl hydrocarbon receptor nuclear translocator in rat brain and pituitary [J].
Huang, P ;
Rannug, A ;
Ahlbom, E ;
Håkansson, H ;
Ceccatelli, S .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2000, 169 (02) :159-167