Literature DB >> 17316558

Increased susceptibility of MER5 (peroxiredoxin III) knockout mice to LPS-induced oxidative stress.

Lianqin Li1, Wataru Shoji, Hirohisa Takano, Noriko Nishimura, Yasunobu Aoki, Ryoya Takahashi, Sataro Goto, Tomonori Kaifu, Toshiyuki Takai, Masuo Obinata.   

Abstract

MER5 (also called peroxiredoxin III, PrxIII) is a member of peroxiredoxin family that has antioxidant activity. The present study was performed to investigate its in vivo function using MER5 knockout mice. MER5 knockout mice were born in normal frequency and could grow to maturity, but we found that intracellular ROS levels are significantly higher in the macrophages of the knockout mice. We examined roles of MER5 function for the oxidative stress responses by intratracheal inoculation of lipopolysaccharide (LPS) to the mice. Lung inflammation such as inflammatory cell infiltration and airway wall thickening was more severely detected in the knockout mice. At the same time, oxidative damage on DNA and proteins was more strongly detected in lung tissues of the knockout mice, including 8-hydroxy-2'-deoxyguanosine (8-OHdG) formation and protein carbonylation. The degrees of lung inflammation and oxidative damage were positively related with LPS doses. Our results indicate that MER5 knockout mice accumulated higher intracellular ROS levels, which cause LPS-induced lung injury more severely, and thus, suggested that MER5 acts as an important scavenger of reactive oxygen species (ROS) under oxidative stress.

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Year:  2007        PMID: 17316558     DOI: 10.1016/j.bbrc.2007.02.022

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  52 in total

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Review 2.  Redox biology of the intestine.

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Review 3.  Mitochondrial thiols in the regulation of cell death pathways.

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Journal:  Antioxid Redox Signal       Date:  2012-06-11       Impact factor: 8.401

4.  Knockout of mitochondrial thioredoxin reductase stabilizes prolyl hydroxylase 2 and inhibits tumor growth and tumor-derived angiogenesis.

Authors:  Juliane Hellfritsch; Julian Kirsch; Manuela Schneider; Tamara Fluege; Markus Wortmann; Jeroen Frijhoff; Markus Dagnell; Theres Fey; Irene Esposito; Pirkko Kölle; Kristin Pogoda; José Pedro Friedmann Angeli; Irina Ingold; Peter Kuhlencordt; Arne Östman; Ulrich Pohl; Marcus Conrad; Heike Beck
Journal:  Antioxid Redox Signal       Date:  2015-04-10       Impact factor: 8.401

Review 5.  Mitochondrial energetics and therapeutics.

Authors:  Douglas C Wallace; Weiwei Fan; Vincent Procaccio
Journal:  Annu Rev Pathol       Date:  2010       Impact factor: 23.472

Review 6.  The sulfiredoxin-peroxiredoxin (Srx-Prx) axis in cell signal transduction and cancer development.

Authors:  Murli Mishra; Hong Jiang; Lisha Wu; Hedy A Chawsheen; Qiou Wei
Journal:  Cancer Lett       Date:  2015-07-10       Impact factor: 8.679

Review 7.  Mitochondrial ROS control of cancer.

Authors:  María Del Pilar Sosa Idelchik; Ulrike Begley; Thomas J Begley; J Andrés Melendez
Journal:  Semin Cancer Biol       Date:  2017-04-23       Impact factor: 15.707

8.  Mitochondrial quality control in alveolar epithelial cells damaged by S. aureus pneumonia in mice.

Authors:  Hagir B Suliman; Bryan Kraft; Raquel Bartz; Lingye Chen; Karen E Welty-Wolf; Claude A Piantadosi
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2017-06-29       Impact factor: 5.464

9.  Sulfiredoxin Translocation into Mitochondria Plays a Crucial Role in Reducing Hyperoxidized Peroxiredoxin III.

Authors:  You Hyun Noh; Jin Young Baek; Woojin Jeong; Sue Goo Rhee; Tong-Shin Chang
Journal:  J Biol Chem       Date:  2009-01-28       Impact factor: 5.157

10.  Role of peroxiredoxin III in the pathogenesis of pre-eclampsia as evidenced in mice.

Authors:  Lianqin Li; Masuo Obinata; Katsuyoshi Hori
Journal:  Oxid Med Cell Longev       Date:  2010 Jan-Feb       Impact factor: 6.543

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