» Articles » PMID: 26222895

Membrane Turnover and Receptor Trafficking in Regenerating Axons

Overview
Journal Eur J Neurosci
Specialty Neurology
Date 2015 Jul 30
PMID 26222895
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Peripheral axonal regeneration requires surface-expanding membrane addition. The continuous incorporation of new membranes into the axolemma allows the pushing force of elongating microtubules to drive axonal growth cones forwards. Hence, a constant supply of membranes and cytoskeletal building blocks is required, often for many weeks. In human peripheral nerves, axonal tips may be more than 1 m away from the neuronal cell body. Therefore, in the initial phase of regeneration, membranes are derived from pre-existing vesicles or synthesised locally. Only later stages of axonal regeneration are supported by membranes and proteins synthesised in neuronal cell bodies, considering that the fastest anterograde transport mechanisms deliver cargo at 20 cm/day. Whereas endocytosis and exocytosis of membrane vesicles are balanced in intact axons, membrane incorporation exceeds membrane retrieval during regeneration to compensate for the loss of membranes distal to the lesion site. Physiological membrane turnover rates will not be established before the completion of target reinnervation. In this review, the current knowledge on membrane traffic in axonal outgrowth is summarised, with a focus on endosomal vesicles as the providers of membranes and carriers of growth factor receptors required for initiating signalling pathways to promote the elongation and branching of regenerating axons in lesioned peripheral nerves.

Citing Articles

TOM-1/tomosyn acts with the UNC-6/netrin receptor UNC-5 to inhibit growth cone protrusion in Caenorhabditis elegans.

Mahadik S, Lundquist E Development. 2023; 150(7).

PMID: 37014062 PMC: 10112904. DOI: 10.1242/dev.201031.


Selective axonal transport through branch junctions is directed by growth cone signaling and mediated by KIF1/kinesin-3 motors.

Tymanskyj S, Curran B, Ma L Cell Rep. 2022; 39(4):110748.

PMID: 35476993 PMC: 9097860. DOI: 10.1016/j.celrep.2022.110748.


Fibroblast Growth Factor Signalling in the Diseased Nervous System.

Klimaschewski L, Claus P Mol Neurobiol. 2021; 58(8):3884-3902.

PMID: 33860438 PMC: 8280051. DOI: 10.1007/s12035-021-02367-0.


Axonal Organelles as Molecular Platforms for Axon Growth and Regeneration after Injury.

Petrova V, Nieuwenhuis B, Fawcett J, Eva R Int J Mol Sci. 2021; 22(4).

PMID: 33670312 PMC: 7918155. DOI: 10.3390/ijms22041798.


Hyperactive and impulsive behaviors of LMTK1 knockout mice.

Takahashi M, Sugiyama A, Wei R, Kobayashi S, Fukuda K, Nishino H Sci Rep. 2020; 10(1):15461.

PMID: 32963255 PMC: 7508861. DOI: 10.1038/s41598-020-72304-z.