Literature DB >> 19716514

Aryl hydrocarbon receptor-mediated induction of the cytosolic phospholipase A(2)alpha gene by 2,3,7,8-tetrachlorodibenzo-p-dioxin in mouse hepatoma Hepa-1c1c7 cells.

Masaki Kinehara1, Itsuko Fukuda, Ken-ichi Yoshida, Hitoshi Ashida.   

Abstract

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 A(2)s (PLA(2)s) 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 A(2)alpha (cPLA(2)alpha), 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 PLA(2,) while this increased expression was not observed in AhR-defective c12 cells. After transient transfection of an Ahr gene-expressing plasmid into the c12 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.

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Year:  2009        PMID: 19716514     DOI: 10.1016/j.jbiosc.2009.04.015

Source DB:  PubMed          Journal:  J Biosci Bioeng        ISSN: 1347-4421            Impact factor:   2.894


  9 in total

Review 1.  Cytosolic phospholipase A₂: physiological function and role in disease.

Authors:  Christina C Leslie
Journal:  J Lipid Res       Date:  2015-04-02       Impact factor: 5.922

Review 2.  The role of AHR-inducible cytochrome P450s in metabolism of polyunsaturated fatty acids.

Authors:  Oliver Hankinson
Journal:  Drug Metab Rev       Date:  2016-06-30       Impact factor: 4.518

Review 3.  Exactly the same but different: promiscuity and diversity in the molecular mechanisms of action of the aryl hydrocarbon (dioxin) receptor.

Authors:  Michael S Denison; Anatoly A Soshilov; Guochun He; Danica E DeGroot; Bin Zhao
Journal:  Toxicol Sci       Date:  2011-09-09       Impact factor: 4.849

4.  Nucleotide specificity of DNA binding of the aryl hydrocarbon receptor:ARNT complex is unaffected by ligand structure.

Authors:  Danica E DeGroot; Michael S Denison
Journal:  Toxicol Sci       Date:  2013-10-17       Impact factor: 4.849

5.  An untargeted multi-technique metabolomics approach to studying intracellular metabolites of HepG2 cells exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin.

Authors:  Ainhoa Ruiz-Aracama; Ad Peijnenburg; Jos Kleinjans; Danyel Jennen; Joost van Delft; Caroline Hellfrisch; Arjen Lommen
Journal:  BMC Genomics       Date:  2011-05-20       Impact factor: 3.969

6.  Predominant role of cytosolic phospholipase A2α in dioxin-induced neonatal hydronephrosis in mice.

Authors:  Wataru Yoshioka; Tatsuya Kawaguchi; Nozomi Fujisawa; Keiko Aida-Yasuoka; Takao Shimizu; Fumio Matsumura; Chiharu Tohyama
Journal:  Sci Rep       Date:  2014-02-10       Impact factor: 4.379

7.  Roles of cytosolic phospholipase A2α in reproductive and systemic toxicities in 2,3,7,8-tetrachlorodibenzo-p-dioxin-exposed mice.

Authors:  Nozomi Fujisawa; Wataru Yoshioka; Hiroyuki Yanagisawa; Chiharu Tohyama
Journal:  Arch Toxicol       Date:  2017-10-17       Impact factor: 5.153

Review 8.  Mechanisms of Developmental Toxicity of Dioxins and Related Compounds.

Authors:  Wataru Yoshioka; Chiharu Tohyama
Journal:  Int J Mol Sci       Date:  2019-01-31       Impact factor: 5.923

9.  Reversal of obesity and liver steatosis in mice via inhibition of aryl hydrocarbon receptor and altered gene expression of CYP1B1, PPARα, SCD1, and osteopontin.

Authors:  Itzel Y Rojas; Benjamin J Moyer; Carol S Ringelberg; Craig R Tomlinson
Journal:  Int J Obes (Lond)       Date:  2020-01-07       Impact factor: 5.095

  9 in total

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