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Miro, MCU, and calcium: Bridging our understanding of mitochondrial movement in axons

Author(s)
Niescier, Robert F.Chang, Karen T.Min, Kyung-Tai
Issued Date
2013-09
DOI
10.3389/fncel.2013.00148
URI
https://scholarworks.unist.ac.kr/handle/201301/2515
Fulltext
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84885070787
Citation
FRONTIERS IN CELLULAR NEUROSCIENCE, v.7, pp.1 - 5
Abstract
Neurons are extremely polarized structures with long axons and dendrites, which require proper distribution of mitochondria and maintenance of mitochondrial dynamics for neuronal functions and survival. Indeed, recent studies show that various neurological disorders are linked to mitochondrial transport in neurons. Mitochondrial anterograde transport is believed to deliver metabolic energy to synaptic terminals where energy demands are high, while mitochondrial retrograde transport is required to repair or remove damaged mitochondria in axons. It has been suggested that Ca2+ plays a key role in regulating mitochondrial transport by altering the configuration of mitochondrial protein, miro. However, molecular mechanisms that regulate mitochondrial transport in neurons still are not well characterized. In this review, we will discuss the roles of miro in mitochondrial transport and how the recently identified components of the mitochondrial calcium uniporter add to our current model of mitochondrial mobility regulation.
Publisher
FRONTIERS RES FOUND
ISSN
1662-5102
Keyword (Author)
Axonal transportMCUMICU1MiroMitochondria

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