Literature DB >> 12531391

Accumulation of 8-oxoguanine in the cellular DNA and the alteration of the OGG1 expression during ischemia-reperfusion injury in the rat kidney.

Kazuhiko Tsuruya1, Masato Furuichi, Yohei Tominaga, Michiya Shinozaki, Masanori Tokumoto, Takahiro Yoshimitsu, Kyoichi Fukuda, Hidetoshi Kanai, Hideki Hirakata, Mitsuo Iida, Yusaku Nakabeppu.   

Abstract

During ischemia-reperfusion (I/R) injury in the rat kidney, apoptosis was observed in the distal tubules of the cortico-medullary region and outer medulla (OM) while severe necrosis was seen in the proximal straight tubules of the OM. The majority of these changes disappeared within 2 weeks. We examined the contents of 8-oxo-2'-deoxyguanosine (8-oxo-dG), which is a major type of oxidative damage in DNA, in the rat kidney during I/R injury, and also investigated the expression level of the OGG1 gene encoding the 8-oxoguanine DNA glycosylase. High-performance liquid chromatography with an MS/MS analysis of the nuclear DNA revealed an immediate accumulation of 8-oxo-dG in the nuclear DNA prepared from the cortex and OM of the kidney 1h after I/R, and an immunohistochemical analysis demonstrated the immediate accumulation of 8-oxo-dG in the nuclei of renal tubular cells both in the cortex and OM. A delayed increase of cytoplasmic staining with anti-8-oxo-dG was observed only in the cortico-medulla and OM, where the cytoplasmic staining in the proximal tubular cells is higher than in the distal tubular cells. The level of cytoplasmic staining representing 8-oxo-dG in mitochondrial DNA, peaked at 6h after I/R and preceded the necrosis of proximal tubular cells in the OM. An RNase protection assay showed a high level of OGG1 mRNA in the normal kidney, and the level decreased within 3h only in the OM, and increased thereafter 1-7 days of I/R both in the cortex and OM. In situ hybridization showed higher levels of OGG1 mRNA expression in the renal tubules in the OM than in the cortex of the normal kidney, which decreased rapidly within 3h of I/R. Thus, the accumulation of 8-oxo-dG in the mitochondrial DNA rather than in nuclear DNA is likely to be involved in the pathogenic responses such as necrosis of renal tubular cells during I/R injury of the kidney, together with an altered level of OGG1 expression.

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Year:  2003        PMID: 12531391     DOI: 10.1016/s1568-7864(02)00214-8

Source DB:  PubMed          Journal:  DNA Repair (Amst)        ISSN: 1568-7856


  28 in total

1.  Nitrative and oxidative DNA damage as potential survival biomarkers for nasopharyngeal carcinoma.

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Journal:  Med Oncol       Date:  2010-03-26       Impact factor: 3.064

2.  Determination of 8-oxoguanine and 8-hydroxy-2'-deoxyguanosine in the rat cerebral cortex using microdialysis sampling and capillary electrophoresis with electrochemical detection.

Authors:  Stacy D Arnett; Damon M Osbourn; Kimberly D Moore; Shannon S Vandaveer; Craig E Lunte
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2005-07-01       Impact factor: 3.205

3.  Site-directed photoproteolysis of 8-oxoguanine DNA glycosylase 1 (OGG1) by specific porphyrin-protein probe conjugates: a strategy to improve the effectiveness of photodynamic therapy for cancer.

Authors:  Kimberly A Conlon; Miguel Berrios
Journal:  J Photochem Photobiol B       Date:  2006-12-15       Impact factor: 6.252

4.  Xanthine oxidoreductase depletion induces renal interstitial fibrosis through aberrant lipid and purine accumulation in renal tubules.

Authors:  Toshio Ohtsubo; Kiyoshi Matsumura; Kanae Sakagami; Koji Fujii; Kazuhiko Tsuruya; Hideko Noguchi; Ilsa I Rovira; Toren Finkel; Mitsuo Iida
Journal:  Hypertension       Date:  2009-08-10       Impact factor: 10.190

Review 5.  The role of DNA base excision repair in brain homeostasis and disease.

Authors:  Mansour Akbari; Marya Morevati; Deborah Croteau; Vilhelm A Bohr
Journal:  DNA Repair (Amst)       Date:  2015-05-01

6.  8-Oxoguanine causes neurodegeneration during MUTYH-mediated DNA base excision repair.

Authors:  Zijing Sheng; Sugako Oka; Daisuke Tsuchimoto; Nona Abolhassani; Hiroko Nomaru; Kunihiko Sakumi; Hidetaka Yamada; Yusaku Nakabeppu
Journal:  J Clin Invest       Date:  2012-11-12       Impact factor: 14.808

7.  A genome-wide distribution of 8-oxoguanine correlates with the preferred regions for recombination and single nucleotide polymorphism in the human genome.

Authors:  Mizuki Ohno; Tomofumi Miura; Masato Furuichi; Yohei Tominaga; Daisuke Tsuchimoto; Kunihiko Sakumi; Yusaku Nakabeppu
Journal:  Genome Res       Date:  2006-05       Impact factor: 9.043

8.  NUDT16 is a (deoxy)inosine diphosphatase, and its deficiency induces accumulation of single-strand breaks in nuclear DNA and growth arrest.

Authors:  Teruaki Iyama; Nona Abolhassani; Daisuke Tsuchimoto; Mari Nonaka; Yusaku Nakabeppu
Journal:  Nucleic Acids Res       Date:  2010-04-12       Impact factor: 16.971

9.  OGG1 is degraded by calpain following oxidative stress and cisplatin exposure.

Authors:  Jeff W Hill; Jennifer J Hu; Michele K Evans
Journal:  DNA Repair (Amst)       Date:  2008-02-21

10.  NUDT16 and ITPA play a dual protective role in maintaining chromosome stability and cell growth by eliminating dIDP/IDP and dITP/ITP from nucleotide pools in mammals.

Authors:  Nona Abolhassani; Teruaki Iyama; Daisuke Tsuchimoto; Kunihiko Sakumi; Mizuki Ohno; Mehrdad Behmanesh; Yusaku Nakabeppu
Journal:  Nucleic Acids Res       Date:  2010-01-15       Impact factor: 16.971

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