Literature DB >> 12700400

Effects of minimally toxic levels of carbonyl cyanide P-(trifluoromethoxy) phenylhydrazone (FCCP), elucidated through differential gene expression with biochemical and morphological correlations.

Sabu Kuruvilla1, Charles W Qualls, Ronald D Tyler, Sam M Witherspoon, Gina R Benavides, Lawrence W Yoon, Karen Dold, Roger H Brown, Subbiah Sangiah, Kevin T Morgan.   

Abstract

Uncouplers of oxidative phosphorylation have relevance to bioenergetics and obesity. The mechanisms of action of chemical uncouplers of oxidative phosphorylation on biological systems were evaluated using differential gene expression. The transcriptional response in human rhabdomyosarcoma cell line (RD), was elucidated following treatment with carbonyl cyanide p-(trifluoromethoxy) phenylhydrazone (FCCP), a classical uncoupling agent. Changes in mitochondrial membrane potential were used as the biological dosimeter. There was an increase in membrane depolarization with increasing concentrations of FCCP. The concentration at 75% uncoupling (20 microM) was chosen to study gene expression changes, using cDNA-based large-scale differential gene expression (LSDGE) platforms. At the above concentration, subtle light microscopic and clear gene expression changes were observed at 1, 2, and 10 h. Statistically significant transcriptional changes were largely associated with protein synthesis, cell cycle regulation, cytoskeletal proteins, energy metabolism, apoptosis, and inflammatory mediators. Bromodeoxyuridine (BrdU) and propidium iodide (PI) assays revealed cell cycle arrest to occur in the G1 and S phases. There was a significant initial decrease in the intracellular adenosine triphosphate (ATP) concentrations. The following seven genes were selected as potential molecular markers for chemical uncouplers: seryl-tRNA synthetase (Ser-tRS), glutamine-hydrolyzing asparagine synthetase (Glut-HAS), mitochondrial bifunctional methylenetetrahydrofolate dehydrogenase (Mit BMD), mitochondrial heat shock 10-kDa protein (Mit HSP 10), proliferating cyclic nuclear antigen (PCNA), cytoplasmic beta-actin (Act B), and growth arrest and DNA damage-inducible protein 153 (GADD153). Transcriptional changes of all seven genes were later confirmed with reverse transcription-polymerase chain reaction (RT-PCR). These results suggest that gene expression changes may provide a sensitive indicator of uncoupling in response to chemical exposure.

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Year:  2003        PMID: 12700400     DOI: 10.1093/toxsci/kfg084

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  4 in total

1.  Glutathione reductase and a mitochondrial thioredoxin play overlapping roles in maintaining iron-sulfur enzymes in fission yeast.

Authors:  Ji-Yoon Song; Joonseok Cha; Joon Lee; Jung-Hye Roe
Journal:  Eukaryot Cell       Date:  2006-09-01

2.  SR4 Uncouples Mitochondrial Oxidative Phosphorylation, Modulates AMP-dependent Kinase (AMPK)-Mammalian Target of Rapamycin (mTOR) Signaling, and Inhibits Proliferation of HepG2 Hepatocarcinoma Cells.

Authors:  James L Figarola; Jyotsana Singhal; Joshua D Tompkins; George W Rogers; Charles Warden; David Horne; Arthur D Riggs; Sanjay Awasthi; Sharad S Singhal
Journal:  J Biol Chem       Date:  2015-11-03       Impact factor: 5.157

3.  Safety evaluation of chinese medicine injections with a cell imaging-based multiparametric assay revealed a critical involvement of mitochondrial function in hepatotoxicity.

Authors:  Meng Wang; Chen-Xiang Liu; Ran-Ran Dong; Shuang He; Ting-Ting Liu; Tie-Chan Zhao; Zhi-Long Wang; Xi-Ya Shen; Bo-Li Zhang; Xiu-Mei Gao; Yan Zhu
Journal:  Evid Based Complement Alternat Med       Date:  2015-02-22       Impact factor: 2.629

4.  Quantitative Proteomic Profiling of Mitochondrial Toxicants in a Human Cardiomyocyte Cell Line.

Authors:  Zhengxi Wei; Jinghua Zhao; Jake Niebler; Jian-Jiang Hao; B Alex Merrick; Menghang Xia
Journal:  Front Genet       Date:  2020-07-07       Impact factor: 4.599

  4 in total

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