Literature DB >> 12504824

Mitochondrial DNA mutations activate the mitochondrial apoptotic pathway and cause dilated cardiomyopathy.

Dekui Zhang1, Justin L Mott, Patricia Farrar, Jan S Ryerse, Shin-Wen Chang, Melissa Stevens, Grace Denniger, Hans Peter Zassenhaus.   

Abstract

OBJECTIVE: To determine whether low frequency mitochondrial DNA (mtDNA) mutations are pathogenic.
METHODS: We studied mice that express a proofreading-deficient mitochondrial DNA polymerase in the heart and develop cardiac mtDNA mutations.
RESULTS: At 4 weeks of age, when point mutation levels had risen to on average two per mitochondrial genome, these mice developed severe dilated cardiomyopathy. Interstitial fibrosis first became apparent at 4 weeks of age and progressed with age. Sporadic myocytic death occurred in all regions of the heart, apparently due to apoptosis as assessed by histological analysis and TUNEL staining. The frequency of TUNEL-positive cells peaked at 4-5 weeks of age and then gradually declined. While mitochondrial respiratory function, ultrastructure, and number remained normal, cytochrome c was released from mitochondria, a known apoptotic signal.
CONCLUSION: mtDNA mutations therefore are pathogenic, and seem to trigger apoptosis through the mitochondrial pathway.

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Year:  2003        PMID: 12504824     DOI: 10.1016/s0008-6363(02)00695-8

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN: 0008-6363            Impact factor:   10.787


  26 in total

1.  Age-dependent cardiomyopathy in mitochondrial mutator mice is attenuated by overexpression of catalase targeted to mitochondria.

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Review 4.  Mitochondrial centrality in heart failure.

Authors:  José Marín-García; Michael J Goldenthal
Journal:  Heart Fail Rev       Date:  2008-01-05       Impact factor: 4.214

Review 5.  Amelioration of premature aging in mtDNA mutator mouse by exercise: the interplay of oxidative stress, PGC-1α, p53, and DNA damage. A hypothesis.

Authors:  Adeel Safdar; Sofia Annis; Yevgenya Kraytsberg; Chloe Laverack; Ayesha Saleem; Konstantin Popadin; Dori C Woods; Jonathan L Tilly; Konstantin Khrapko
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6.  p53-PGC-1α pathway mediates oxidative mitochondrial damage and cardiomyocyte necrosis induced by monoamine oxidase-A upregulation: role in chronic left ventricular dysfunction in mice.

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Journal:  Antioxid Redox Signal       Date:  2012-08-10       Impact factor: 8.401

7.  Mitochondria DNA mutations cause sex-dependent development of hypertension and alterations in cardiovascular function.

Authors:  Mark J Golob; Lian Tian; Zhijie Wang; Todd A Zimmerman; Christine A Caneba; Timothy A Hacker; Guoqing Song; Naomi C Chesler
Journal:  J Biomech       Date:  2014-12-31       Impact factor: 2.712

8.  Mitochondrial DNA polymerase editing mutation, PolgD257A, disturbs stem-progenitor cell cycling in the small intestine and restricts excess fat absorption.

Authors:  Raymond G Fox; Scott Magness; Gregory C Kujoth; Tomas A Prolla; Nobuyo Maeda
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2012-02-16       Impact factor: 4.052

9.  Chronically elevated glucose compromises myocardial mitochondrial DNA integrity by alteration of mitochondrial topoisomerase function.

Authors:  S Medikayala; B Piteo; X Zhao; J G Edwards
Journal:  Am J Physiol Cell Physiol       Date:  2010-12-01       Impact factor: 4.249

Review 10.  The role of mitochondrial DNA mutations in aging and sarcopenia: implications for the mitochondrial vicious cycle theory of aging.

Authors:  Asimina Hiona; Christiaan Leeuwenburgh
Journal:  Exp Gerontol       Date:  2007-10-04       Impact factor: 4.032

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