Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family.

Abstract

BACKGROUND Cerebral autosomal arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is characterized by recurrent subcortical ischemic strokes and dementia caused by mutations in the Notch3 gene. In Drosophila melanogaster, Notch signaling has a pleiotropic effect, affecting most tissues of the organism during development. OBJECTIVE To characterize a potential mitochondrial dysfunction associated with mutations in the Notch3 gene. METHODS Biochemical, histochemical, molecular, and genetic analyses were performed on muscle biopsy specimens and fibroblasts obtained from patients of a Spanish family with CADASIL. Additional biochemical and molecular analyses of the N(55e11) mutant of D. melanogaster were performed. RESULTS In muscle biopsy specimens, a significant decrease was found in the activity of complex I (NADH [reduced form of nicotinamide adenine dinucleotide] dehydrogenase), and in one patient, histochemical analysis showed the presence of ragged-red fibers with abnormal cytochrome c oxidase staining. Reduced fibroblast activity of complex V (ATP synthase) was found. Supporting data on patients with CADASIL, it was found that the mutation N(55e11) in Drosophila decreases the activity of mitochondrial respiratory complexes I and V. CONCLUSIONS Mitochondrial respiratory chain activity responds, directly or indirectly, to the Notch signaling pathway. Mitochondrial dysfunction in patients with CADASIL may be an epiphenomenon, but results of this study suggest that the pathophysiology of the disease could include a defect in oxidative phosphorylation.

Statistics

0100200'05'06'07'08'09'10'11'12'13'14'15'16'17
Citations per Year

636 Citations

Semantic Scholar estimates that this publication has 636 citations based on the available data.

See our FAQ for additional information.

Cite this paper

@article{Pea2001MitochondrialDA, title={Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family.}, author={Pilar de la Pe{\~n}a and Bel{\'e}n {\'A}lvarez Bornstein and Pilar del Hoyo and Miguel {\'A}ngel Fern{\'a}ndez-Moreno and Miguel Angel Mart{\'i}n and Yolanda C. Campos and Carlos G{\'o}mez-Escalonilla and Jose Antonio Navas Molina and Ana Cabello and Joaqu{\'i}n Arenas and Rafael Garesse}, journal={Neurology}, year={2001}, volume={57 7}, pages={1235-8} }