Literature DB >> 17444508

Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease.

Dominique Loiseau1, Arnaud Chevrollier, Christophe Verny, Virginie Guillet, Naïg Gueguen, Marie-Anne Pou de Crescenzo, Marc Ferré, Marie-Claire Malinge, Agnès Guichet, Guillaume Nicolas, Patrizia Amati-Bonneau, Yves Malthièry, Dominique Bonneau, Pascal Reynier.   

Abstract

OBJECTIVE: Mutations of the mitofusin 2 gene (MFN2) may account for at least a third of the cases of Charcot-Marie-Tooth disease type 2 (CMT2). This study investigates mitochondrial cellular bioenergetics in MFN2-related CMT2A.
METHODS: Mitochondrial network morphology and metabolism were studied in cultures of skin fibroblasts obtained from four CMT2A patients harboring novel missense mutations of the MFN2 gene.
RESULTS: Although the mitochondrial network appeared morphologically unaltered, there was a significant defect of mitochondrial coupling associated with a reduction of the mitochondrial membrane potential.
INTERPRETATION: Our results suggest that the sharply reduced efficacy of oxidative phosphorylation in MFN2-related CMT2A may contribute to the pathophysiology of the axonal neuropathy.

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Year:  2007        PMID: 17444508     DOI: 10.1002/ana.21086

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  45 in total

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Review 5.  Ophthalmic manifestations of inherited neurodegenerative disorders.

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Review 7.  Diagnosis of Charcot-Marie-Tooth disease.

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9.  Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A disease.

Authors:  Virginie Guillet; Naïg Gueguen; Christophe Verny; Marc Ferre; Chadi Homedan; Dominique Loiseau; Vincent Procaccio; Patrizia Amati-Bonneau; Dominique Bonneau; Pascal Reynier; Arnaud Chevrollier
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10.  Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).

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Journal:  Neurogenetics       Date:  2008-12-17       Impact factor: 2.660

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