Literature DB >> 11092892

Selective targeting of a redox-active ubiquinone to mitochondria within cells: antioxidant and antiapoptotic properties.

G F Kelso1, C M Porteous, C V Coulter, G Hughes, W K Porteous, E C Ledgerwood, R A Smith, M P Murphy.   

Abstract

With the recognition of the central role of mitochondria in apoptosis, there is a need to develop specific tools to manipulate mitochondrial function within cells. Here we report on the development of a novel antioxidant that selectively blocks mitochondrial oxidative damage, enabling the roles of mitochondrial oxidative stress in different types of cell death to be inferred. This antioxidant, named mitoQ, is a ubiquinone derivative targeted to mitochondria by covalent attachment to a lipophilic triphenylphosphonium cation through an aliphatic carbon chain. Due to the large mitochondrial membrane potential, the cation was accumulated within mitochondria inside cells, where the ubiquinone moiety inserted into the lipid bilayer and was reduced by the respiratory chain. The ubiquinol derivative thus formed was an effective antioxidant that prevented lipid peroxidation and protected mitochondria from oxidative damage. After detoxifying a reactive oxygen species, the ubiquinol moiety was regenerated by the respiratory chain enabling its antioxidant activity to be recycled. In cell culture studies, the mitochondrially localized antioxidant protected mammalian cells from hydrogen peroxide-induced apoptosis but not from apoptosis induced by staurosporine or tumor necrosis factor-alpha. This was compared with untargeted ubiquinone analogs, which were ineffective in preventing apoptosis. These results suggest that mitochondrial oxidative stress may be a critical step in apoptosis induced by hydrogen peroxide but not for apoptosis induced by staurosporine or tumor necrosis factor-alpha. We have shown that selectively manipulating mitochondrial antioxidant status with targeted and recyclable antioxidants is a feasible approach to investigate the role of mitochondrial oxidative damage in apoptotic cell death. This approach will have further applications in investigating mitochondrial dysfunction in a range of experimental models.

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Year:  2000        PMID: 11092892     DOI: 10.1074/jbc.M009093200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  327 in total

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Authors:  Brian D Fink; Judith A Herlein; Mark A Yorek; Amanda M Fenner; Robert J Kerns; William I Sivitz
Journal:  J Pharmacol Exp Ther       Date:  2012-06-01       Impact factor: 4.030

2.  Granzyme B-induced mitochondrial ROS are required for apoptosis.

Authors:  G Jacquemin; D Margiotta; A Kasahara; E Y Bassoy; M Walch; J Thiery; J Lieberman; D Martinvalet
Journal:  Cell Death Differ       Date:  2014-10-31       Impact factor: 15.828

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Authors:  David J Rowlands; Mohammad Naimul Islam; Shonit R Das; Alice Huertas; Sadiqa K Quadri; Keisuke Horiuchi; Nilufar Inamdar; Memet T Emin; Jens Lindert; Vadim S Ten; Sunita Bhattacharya; Jahar Bhattacharya
Journal:  J Clin Invest       Date:  2011-04-25       Impact factor: 14.808

Review 4.  Friedreich ataxia-update on pathogenesis and possible therapies.

Authors:  Max Voncken; Panos Ioannou; Martin B Delatycki
Journal:  Neurogenetics       Date:  2003-12-19       Impact factor: 2.660

Review 5.  Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms.

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Journal:  J Inherit Metab Dis       Date:  2017-05-17       Impact factor: 4.982

Review 6.  Melatonin as a mitochondria-targeted antioxidant: one of evolution's best ideas.

Authors:  Russel J Reiter; Sergio Rosales-Corral; Dun Xian Tan; Mei Jie Jou; Annia Galano; Bing Xu
Journal:  Cell Mol Life Sci       Date:  2017-09-01       Impact factor: 9.261

7.  The mitochondrial antioxidants MitoE(2) and MitoQ(10) increase mitochondrial Ca(2+) load upon cell stimulation by inhibiting Ca(2+) efflux from the organelle.

Authors:  Sara Leo; György Szabadkai; Rosario Rizzuto
Journal:  Ann N Y Acad Sci       Date:  2008-12       Impact factor: 5.691

8.  Synergy between docosahexaenoic acid and butyrate elicits p53-independent apoptosis via mitochondrial Ca(2+) accumulation in colonocytes.

Authors:  Satya Sree N Kolar; Rola Barhoumi; Evelyn S Callaway; Yang-Yi Fan; Naisyin Wang; Joanne R Lupton; Robert S Chapkin
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2007-08-23       Impact factor: 4.052

9.  Beta-amyloid mediated nitration of manganese superoxide dismutase: implication for oxidative stress in a APPNLH/NLH X PS-1P264L/P264L double knock-in mouse model of Alzheimer's disease.

Authors:  Muthuswamy Anantharaman; Jitbanjong Tangpong; Jeffery N Keller; Michael P Murphy; William R Markesbery; Kelley K Kiningham; Daret K St Clair
Journal:  Am J Pathol       Date:  2006-05       Impact factor: 4.307

10.  Peroxiredoxin-5 targeted to the mitochondrial intermembrane space attenuates hypoxia-induced reactive oxygen species signalling.

Authors:  Simran S Sabharwal; Gregory B Waypa; Jeremy D Marks; Paul T Schumacker
Journal:  Biochem J       Date:  2013-12-15       Impact factor: 3.857

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