Literature DB >> 15100242

Tissue-specific expression and subcellular distribution of murine glutathione S-transferase class kappa.

Rachel E Thomson1, Alison L Bigley, John R Foster, Ian R Jowsey, Clifford R Elcombe, Terry C Orton, John D Hayes.   

Abstract

Class kappa glutathione S-transferases are a poorly characterized family of detoxication enzymes whose localization has not been defined. In this study we investigated the tissue, cellular, and subcellular distribution of mouse glutathione S-transferase class kappa 1 (mGSTK1) protein using a variety of immunolocalization techniques. Western blotting analysis of mouse tissue homogenates demonstrated that mGSTK1 is expressed at relatively high levels in liver and stomach. Moderate expression was observed in kidney, heart, large intestine, testis, and lung, whereas sparse or essentially no mGSTK1 protein was detected in small intestine, brain, spleen, and skeletal muscle. Immunohistochemical (IHC) analysis for mGSTK1 revealed granular staining of hepatocytes throughout the liver, consistent with organelle staining. IHC analysis of murine kidney localized GSTK1 to the straight portion of the proximal convoluted tubule (pars recta). Staining was consistent with regions rich in mitochondria. Electron microscopy, using indirect immunocolloidal gold staining, clearly showed that mGSTK1 was localized in mitochondria in both mouse liver and kidney. These results are consistent with a role for mGST K1-1 in detoxification, and the confirmation of the intramitochondrial localization of this enzyme implies a unique role for GST class kappa as an antioxidant enzyme.

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Year:  2004        PMID: 15100242     DOI: 10.1177/002215540405200509

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  12 in total

1.  Proteomic analysis of glutathione S-transferase isoforms in mouse liver mitochondria.

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Review 2.  Dual localization of glutathione S-transferase in the cytosol and mitochondria: implications in oxidative stress, toxicity and disease.

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Journal:  FEBS J       Date:  2011-10-12       Impact factor: 5.542

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Journal:  Mol Cell Proteomics       Date:  2016-05-27       Impact factor: 5.911

4.  Endoplasmic reticulum (ER) localization is critical for DsbA-L protein to suppress ER stress and adiponectin down-regulation in adipocytes.

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Journal:  J Biol Chem       Date:  2015-03-04       Impact factor: 5.157

5.  Hepatic DsbA-L protects mice from diet-induced hepatosteatosis and insulin resistance.

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Journal:  FASEB J       Date:  2017-02-23       Impact factor: 5.191

Review 6.  Mitochondria-Associated Endoplasmic Reticulum Membranes (MAMs) and Their Prospective Roles in Kidney Disease.

Authors:  Peng Gao; Wenxia Yang; Lin Sun
Journal:  Oxid Med Cell Longev       Date:  2020-09-03       Impact factor: 6.543

7.  Characterization of visceral and subcutaneous adipose tissue transcriptome in pregnant women with and without spontaneous labor at term: implication of alternative splicing in the metabolic adaptations of adipose tissue to parturition.

Authors:  Shali Mazaki-Tovi; Adi L Tarca; Edi Vaisbuch; Juan Pedro Kusanovic; Nandor Gabor Than; Tinnakorn Chaiworapongsa; Zhong Dong; Sonia S Hassan; Roberto Romero
Journal:  J Perinat Med       Date:  2016-10-01       Impact factor: 1.901

8.  Glutathione S-Transferase Protein Expression in Different Life Stages of Zebrafish (Danio rerio).

Authors:  Alena Tierbach; Ksenia J Groh; René Schönenberger; Kristin Schirmer; Marc J-F Suter
Journal:  Toxicol Sci       Date:  2018-04-01       Impact factor: 4.849

Review 9.  Establishment of metabolism and transport pathways in the rodent and human fetal liver.

Authors:  Jamie E Moscovitz; Lauren M Aleksunes
Journal:  Int J Mol Sci       Date:  2013-12-06       Impact factor: 5.923

10.  Age-associated changes in GSH S-transferase gene/proteins in livers of rats.

Authors:  Shangfu Xu; Dongshun Hou; Jie Liu; Lili Ji
Journal:  Redox Rep       Date:  2018-12       Impact factor: 4.412

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