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Mol Cell Neurosci. 2017 Apr;80:134-147. doi: 10.1016/j.mcn.2017.03.006. Epub 2017 Mar 11.

Developmental changes in trak-mediated mitochondrial transport in neurons.

Author information

1
School of Pharmacy University College London, 29/39 Brunswick Square, London WC1N 1AX, United Kingdom.
2
School of Pharmacy University College London, 29/39 Brunswick Square, London WC1N 1AX, United Kingdom. Electronic address: anne.stephenson@ucl.ac.uk.

Abstract

Previous studies established that the kinesin adaptor proteins, TRAK1 and TRAK2, play an important role in mitochondrial transport in neurons. They link mitochondria to kinesin motor proteins via a TRAK acceptor protein in the mitochondrial outer membrane, the Rho GTPase, Miro. TRAKs also associate with enzyme, O-linked N-acetylglucosamine transferase (OGT), to form a quaternary, mitochondrial trafficking complex. A recent report suggested that TRAK1 preferentially controls mitochondrial transport in axons of hippocampal neurons whereas TRAK2 controls mitochondrial transport in dendrites. However, it is not clear whether the function of any of these proteins is exclusive to axons or dendrites and if their mechanisms of action are conserved between different neuronal populations and also, during maturation. Here, a comparative study was carried out into TRAK-mediated mitochondrial mobility in axons and dendrites of hippocampal and cortical neurons during maturation in vitro using a shRNA gene knockdown approach. It was found that in mature hippocampal and cortical neurons, TRAK1 predominantly mediates axonal mitochondrial transport whereas dendritic transport is mediated via TRAK2. In young, maturing neurons, TRAK1 and TRAK2 contribute similarly in mitochondrial transport in both axons and dendrites in both neuronal types. These findings demonstrate maturation regulation of mitochondrial transport which is conserved between at least two distinct neuronal subtypes.

KEYWORDS:

Axonal transport; Kinesin; Mitochondrial transport; TRAK; Trafficking kinesin binding protein

PMID:
28300646
PMCID:
PMC5400476
DOI:
10.1016/j.mcn.2017.03.006
[Indexed for MEDLINE]
Free PMC Article

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