University of Tasmania
Browse
87024_A1.pdf (3.06 MB)

In-vivo single neuron axotomy triggers axon regeneration to restore synaptic density in specific cortical circuits

Download (3.06 MB)
journal contribution
posted on 2023-05-17, 20:06 authored by Alison CantyAlison Canty, Huang, L, Jackson, JS, Little, GE, Knott, G, Maco, B, De Paola, V
To what extent, how and when axons respond to injury in the highly interconnected grey matter is poorly understood. Here we use two-photon imaging and focused ion beam-scanning electron microscopy to explore, at synaptic resolution, the regrowth capacity of several neuronal populations in the intact brain. Time-lapse analysis of >100 individually ablated axons for periods of up to a year reveals a surprising inability to regenerate even in a glial scar-free environment. However, depending on cell type some axons spontaneously extend for distances unseen in the unlesioned adult cortex and at maximum speeds comparable to peripheral nerve regeneration. Regrowth follows a distinct pattern from developmental axon growth. Remarkably, although never reconnecting to the original targets, axons consistently form new boutons at comparable prelesion synaptic densities, implying the existence of intrinsic homeostatic programmes, which regulate synaptic numbers on regenerating axons. Our results may help guide future clinical investigations to promote functional axon regeneration.

History

Publication title

Nature Communications

Volume

4

Article number

2038

Number

2038

Pagination

1-10

ISSN

2041-1723

Department/School

Tasmanian School of Medicine

Publisher

Nature Publishing Group

Place of publication

United Kingdom

Rights statement

Copyright 2013 Macmillan Publishers Limited. Licensed under Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported (CC BY-NC-ND 3.0) https://creativecommons.org/licenses/by-nc-nd/3.0/

Repository Status

  • Open

Socio-economic Objectives

Clinical health not elsewhere classified

Usage metrics

    University Of Tasmania

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC