In-vivo single neuron axotomy triggers axon regeneration to restore synaptic density in specific cortical circuits
A. J. Canty,
L. Huang,
J. S. Jackson,
G. E. Little,
G. Knott,
B. Maco and
V. De Paola ()
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A. J. Canty: MRC Clinical Science Centre, Faculty of Medicine, Imperial College London
L. Huang: MRC Clinical Science Centre, Faculty of Medicine, Imperial College London
J. S. Jackson: MRC Clinical Science Centre, Faculty of Medicine, Imperial College London
G. E. Little: MRC Clinical Science Centre, Faculty of Medicine, Imperial College London
G. Knott: Centre of Interdisciplinary Electron Microscopy, École Polytechnique Fédérale de Lausanne
B. Maco: Centre of Interdisciplinary Electron Microscopy, École Polytechnique Fédérale de Lausanne
V. De Paola: MRC Clinical Science Centre, Faculty of Medicine, Imperial College London
Nature Communications, 2013, vol. 4, issue 1, 1-10
Abstract:
Abstract 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.
Date: 2013
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms3038
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DOI: 10.1038/ncomms3038
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