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首页> 外文期刊>Journal of Bioscience and Bioengineering >Aryl hydrocarbon receptor-mediated induction of the cytosolic phospholipase A_2α gene by 2,3,7,8-tetrachlorodibenzo-p-dioxin in mouse hepatoma Hepa-1c1c7 cells
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Aryl hydrocarbon receptor-mediated induction of the cytosolic phospholipase A_2α gene by 2,3,7,8-tetrachlorodibenzo-p-dioxin in mouse hepatoma Hepa-1c1c7 cells

机译:2,3,7,8-四氯二苯并-p-二恶英在小鼠肝癌Hepa-1c1c7细胞中的芳烃受体介导的胞质磷脂酶A_2α基因的诱导

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摘要

Upon binding to ligands such as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), an aryl hydrocarbon receptor (AhR) is activated to form a heterodimer with an aryl hydrocarbon receptor nuclear translocator (Arnt). This complex binds to DNA. It has been shown that the AhR bonds to a DNA sequence called the dioxin response element (DRE), which controls the expression of battery genes. It is reported that TCDD releases arachidonic acid from membrane phospholipids via activation of phospholipase A2s (PLA2s) in various cell types. Recently, we demonstrated that the TCDD-activated AhR binds to the second intron of the Pla2g4a gene, which encodes cytosolic phospholipase A2α (cPLA2α), in mouse hepatoma Hepa-1c1c7 cells. This result suggests that Pla2g4a appears to be a target gene of the AhR. In the present study, we investigated whether the transcriptional regulation of Pla2g4a is dependent on the AhR in Hepa-1c1c7 cells. Treatment of the cells with TCDD increased mRNA expression of Pla2g4a and enzymatic activity of PLA2, while this increased expression was not observed in AhR-defective c 12 cells. After transient transfection of an Ahr gene-expressing plasmid into the cl2 cells, expression of Pla2g4a was increased by TCDD. These results indicate that Pla2g4a may be a novel target gene of the AhR, and its transcriptional induction is mediated through binding of the AhR to the second intron of Pla2g4a, although this target site does not have a typical DRE sequence.
机译:与2,3,7,8-四氯二苯并-对-二恶英(TCDD)等配体结合后,芳烃受体(AhR)被激活,与芳烃受体核转运子(Arnt)形成异二聚体。该复合物与DNA结合。已经显示,AhR与称为二恶英响应元件(DRE)的DNA序列结合,该DNA序列控制电池基因的表达。据报道,TCDD通过活化各种细胞类型中的磷脂酶A2s(PLA2s)从膜磷脂中释放花生四烯酸。最近,我们证明TCDD激活的AhR与Pla2g4a基因的第二个内含子结合,该基因在小鼠肝癌Hepa-1c1c7细胞中编码胞质磷脂酶A2α(cPLA2α)。该结果表明Pla2g4a似乎是AhR的靶基因。在本研究中,我们调查了Pla2g4a的转录调控是否依赖于Hepa-1c1c7细胞中的AhR。用TCDD处理细胞增加了Pla2g4a的mRNA表达和PLA2的酶活性,而在AhR缺陷的c 12细胞中未观察到这种增加的表达。将表达Ahr基因的质粒瞬时转染到cl2细胞中后,TCDD使Pla2g4a的表达增加。这些结果表明Pla2g4a可能是AhR的新型靶基因,尽管该靶位点没有典型的DRE序列,但其转录诱导是通过AhR与Pla2g4a的第二个内含子的结合而介导的。

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