A high mitochondrial transport rate characterizes CNS neurons with high axonal regeneration capacity.
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ABSTRACT: Improving axonal transport in the injured and diseased central nervous system has been proposed as a promising strategy to improve neuronal repair. However, the contribution of each cargo to the repair mechanism is unknown. DRG neurons globally increase axonal transport during regeneration. Because the transport of specific cargos after axonal insult has not been examined systematically in a model of enhanced regenerative capacity, it is unknown whether the transport of all cargos would be modulated equally in injured central nervous system neurons. Here, using a microfluidic culture system we compared neurons co-deleted for PTEN and SOCS3, an established model of high axonal regeneration capacity, to control neurons. We measured the axonal transport of three cargos (mitochondria, synaptic
SUBMITTER: Cartoni R
PROVIDER: S-EPMC5604968 | biostudies-literature | 2017
REPOSITORIES: biostudies-literature
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