Title
Mitochondrial Fragmentation In Neurodegeneration
Abstract
Mitochondria are remarkably dynamic organelles that migrate, divide and fuse. Cycles of mitochondrial fission and fusion ensure metabolite and mitochondrial DNA mixing and dictate organelle shape, number and bioenergetic functionality. There is mounting evidence that mitochondrial dysfunction is an early and causal event in neurodegeneration. Mutations in the mitochondrial fusion GTPases mitofusin 2 and optic atrophy 1, neurotoxins and oxidative stress all disrupt the cable-like morphology of functional mitochondria. This results in impaired bioenergetics and mitochondrial migration, and can trigger neurodegeneration. These findings suggest potential new treatment avenues for neurodegenerative diseases. © 2008 Macmillan Publishers Limited. All rights reserved.
Publication Date
7-1-2008
Publication Title
Nature Reviews Neuroscience
Volume
9
Issue
7
Number of Pages
505-518
Document Type
Review
Personal Identifier
scopus
DOI Link
https://doi.org/10.1038/nrn2417
Copyright Status
Unknown
Socpus ID
45749117188 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/45749117188
STARS Citation
Knott, Andrew B.; Perkins, Guy; Schwarzenbacher, Robert; and Bossy-Wetzel, Ella, "Mitochondrial Fragmentation In Neurodegeneration" (2008). Scopus Export 2000s. 10396.
https://stars.library.ucf.edu/scopus2000/10396