Selective rab11 transport and the intrinsic regenerative ability of CNS axons

Neurons lose intrinsic axon regenerative ability with maturation, but the mechanism remains unclear. Using an in-vitro laser axotomy model, we show a progressive decline in the ability of cut CNS axons to form a new growth cone and then elongate. Failure of regeneration was associated with increased...

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Main Authors: Hiroaki Koseki, Matteo Donegá, Brian YH Lam, Veselina Petrova, Susan van Erp, Giles SH Yeo, Jessica CF Kwok, Charles ffrench-Constant, Richard Eva, James W Fawcett
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2017-08-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/26956
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spelling doaj-3a974220a5d34cec928b4d7562efb1b62021-05-05T13:39:48ZengeLife Sciences Publications LtdeLife2050-084X2017-08-01610.7554/eLife.26956Selective rab11 transport and the intrinsic regenerative ability of CNS axonsHiroaki Koseki0Matteo Donegá1Brian YH Lam2Veselina Petrova3Susan van Erp4https://orcid.org/0000-0003-0883-2795Giles SH Yeo5Jessica CF Kwok6Charles ffrench-Constant7Richard Eva8https://orcid.org/0000-0003-0305-0452James W Fawcett9https://orcid.org/0000-0002-7990-4568John van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United KingdomDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, United KingdomMRC Metabolic Diseases Unit, Metabolic Research Laboratories, University of Cambridge, Cambridge, United KingdomJohn van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United KingdomMRC Centre of Regenerative Medicine, University of Edinburgh, Edinburgh, United KingdomMRC Metabolic Diseases Unit, Metabolic Research Laboratories, University of Cambridge, Cambridge, United KingdomJohn van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom; School of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds, United Kingdom; Centre of Reconstructive Neuroscience, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Czech RepublicMRC Centre of Regenerative Medicine, University of Edinburgh, Edinburgh, United KingdomJohn van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United KingdomJohn van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom; Centre of Reconstructive Neuroscience, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Czech RepublicNeurons lose intrinsic axon regenerative ability with maturation, but the mechanism remains unclear. Using an in-vitro laser axotomy model, we show a progressive decline in the ability of cut CNS axons to form a new growth cone and then elongate. Failure of regeneration was associated with increased retraction after axotomy. Transportation into axons becomes selective with maturation; we hypothesized that selective exclusion of molecules needed for growth may contribute to regeneration decline. With neuronal maturity rab11 vesicles (which carry many molecules involved in axon growth) became selectively targeted to the somatodendritic compartment and excluded from axons by predominant retrograde transport However, on overexpression rab11 was mistrafficked into proximal axons, and these axons showed less retraction and enhanced regeneration after axotomy. These results suggest that the decline of intrinsic axon regenerative ability is associated with selective exclusion of key molecules, and that manipulation of transport can enhance regeneration.https://elifesciences.org/articles/26956axon regenerationtraffickingaxonal transportendosomessmall GTPasesaxotomy
collection DOAJ
language English
format Article
sources DOAJ
author Hiroaki Koseki
Matteo Donegá
Brian YH Lam
Veselina Petrova
Susan van Erp
Giles SH Yeo
Jessica CF Kwok
Charles ffrench-Constant
Richard Eva
James W Fawcett
spellingShingle Hiroaki Koseki
Matteo Donegá
Brian YH Lam
Veselina Petrova
Susan van Erp
Giles SH Yeo
Jessica CF Kwok
Charles ffrench-Constant
Richard Eva
James W Fawcett
Selective rab11 transport and the intrinsic regenerative ability of CNS axons
eLife
axon regeneration
trafficking
axonal transport
endosomes
small GTPases
axotomy
author_facet Hiroaki Koseki
Matteo Donegá
Brian YH Lam
Veselina Petrova
Susan van Erp
Giles SH Yeo
Jessica CF Kwok
Charles ffrench-Constant
Richard Eva
James W Fawcett
author_sort Hiroaki Koseki
title Selective rab11 transport and the intrinsic regenerative ability of CNS axons
title_short Selective rab11 transport and the intrinsic regenerative ability of CNS axons
title_full Selective rab11 transport and the intrinsic regenerative ability of CNS axons
title_fullStr Selective rab11 transport and the intrinsic regenerative ability of CNS axons
title_full_unstemmed Selective rab11 transport and the intrinsic regenerative ability of CNS axons
title_sort selective rab11 transport and the intrinsic regenerative ability of cns axons
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2017-08-01
description Neurons lose intrinsic axon regenerative ability with maturation, but the mechanism remains unclear. Using an in-vitro laser axotomy model, we show a progressive decline in the ability of cut CNS axons to form a new growth cone and then elongate. Failure of regeneration was associated with increased retraction after axotomy. Transportation into axons becomes selective with maturation; we hypothesized that selective exclusion of molecules needed for growth may contribute to regeneration decline. With neuronal maturity rab11 vesicles (which carry many molecules involved in axon growth) became selectively targeted to the somatodendritic compartment and excluded from axons by predominant retrograde transport However, on overexpression rab11 was mistrafficked into proximal axons, and these axons showed less retraction and enhanced regeneration after axotomy. These results suggest that the decline of intrinsic axon regenerative ability is associated with selective exclusion of key molecules, and that manipulation of transport can enhance regeneration.
topic axon regeneration
trafficking
axonal transport
endosomes
small GTPases
axotomy
url https://elifesciences.org/articles/26956
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