Identification of genetic networks involved in the cell injury accompanying endoplasmic reticulum stress induced by bisphenol A in testicular Sertoli cells

被引:47
作者
Tabuchi, Yoshiaki [1 ]
Takasaki, Ichiro
Kondo, Takashi
机构
[1] Toyama Univ, Life Sci Res Ctr, Div Mol Genet Res, Toyama 930, Japan
[2] Toyama Univ, Fac Med, Dept Radiol Sci, Toyama 930, Japan
关键词
bisphenol A; gene expression; genetic network; Sertoli cell; cell injury; endoplasmic reticulum stress;
D O I
10.1016/j.bbrc.2006.04.177
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
To identify detailed mechanisms by which bisphenol A (BPA), an endocrine-disrupting chemical, induces cell injury in mouse testicular Sertoli TTE3 cells, we performed genome-wide microarray and computational gene network analyses. BPA (200 PM) significantly decreased cell viability and simultaneously induced an increase in mRNA levels of HSPA5 and DDIT3, endoplasmic reticulum (ER) stress marker genes. Of the 22,690 probe sets analyzed, BPA down-regulated 661 probe sets and up-regulated 604 probe sets by > 2,0-fold. Hierarchical cluster analysis demonstrated nine gene clusters. In decreased gene clusters, two significant genetic networks were associated with cell growth and proliferation and the cell cycle. In increased gene clusters, two significant genetic networks including many basic-region leucine zipper transcription factors were associated with cell death and DNA replication, recombination, and repair. The present results will provide additional novel insights into the detailed molecular mechanisms of cell injury accompanying ER stress induced by BPA in Sertoli cells. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1044 / 1050
页数:7
相关论文
共 33 条
[1]  
Alaoui-Jamali MA, 2003, CANCER RES, V63, P3764
[2]   Functional network analysis reveals extended gliomagenesis pathway maps and three novel MYC-interacting genes in human gliomas [J].
Bredel, M ;
Bredel, C ;
Juric, D ;
Harsh, GR ;
Vogel, H ;
Recht, LD ;
Sikic, BI .
CANCER RESEARCH, 2005, 65 (19) :8679-8689
[3]   Mammalian unfolded protein response inhibits cyclin D1 translation and cell-cycle progression [J].
Brewer, JW ;
Hendershot, LM ;
Sherr, CJ ;
Diehl, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (15) :8505-8510
[4]   Evaluation of chemicals with endocrine modulating activity in a yeast-based steroid hormone receptor gene transcription assay [J].
Gaido, KW ;
Leonard, LS ;
Lovell, S ;
Gould, JC ;
Babai, D ;
Portier, CJ ;
McDonnell, DP .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1997, 143 (01) :205-212
[5]   Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinase [J].
Harding, HP ;
Zhang, YH ;
Ron, D .
NATURE, 1999, 397 (6716) :271-274
[6]   Regulated translation initiation controls stress-induced gene expression in mammalian cells [J].
Harding, HP ;
Novoa, I ;
Zhang, YH ;
Zeng, HQ ;
Wek, R ;
Schapira, M ;
Ron, D .
MOLECULAR CELL, 2000, 6 (05) :1099-1108
[7]   Sulfation of "estrogenic" alkylphenols and 17β-estradiol by human platelet phenol sulfotransferases [J].
Harris, RM ;
Waring, RH ;
Kirk, CJ ;
Hughes, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (01) :159-166
[8]   C/EBP family transcription factors are degraded by the proteasome but stabilized by forming dimer [J].
Hattori, T ;
Ohoka, N ;
Inoue, Y ;
Hayashi, H ;
Onozaki, K .
ONCOGENE, 2003, 22 (09) :1273-1280
[9]   Identification of novel transcriptional networks in response to treatment with the anticarcinogen 3H-1,2-dithiole-3-thione [J].
Huang, Y ;
Yan, J ;
Lubet, R ;
Kensler, TW ;
Sutter, TR .
PHYSIOLOGICAL GENOMICS, 2006, 24 (02) :144-153
[10]   Estrogenic alkylphenols induce cell death by inhibiting testis endoplasmic reticulum Ca2+ pumps [J].
Hughes, PJ ;
McLellan, H ;
Lowes, DA ;
Khan, SZ ;
Bilmen, JG ;
Tovey, SC ;
Godfrey, RE ;
Michell, RH ;
Kirk, CJ ;
Michelangeli, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 277 (03) :568-574