SnoN facilitates axonal regeneration after spinal cord injury.

Adult CNS neurons exhibit a reduced capacity for growth compared to developing neurons, due in part to downregulation of growth-associated genes as development is completed. We tested the hypothesis that SnoN, an embryonically regulated transcription factor that specifies growth of the axonal compar...

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Main Authors: Jiun L Do, Azad Bonni, Mark H Tuszynski
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3732222?pdf=render
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author Jiun L Do
Azad Bonni
Mark H Tuszynski
author_facet Jiun L Do
Azad Bonni
Mark H Tuszynski
author_sort Jiun L Do
collection DOAJ
description Adult CNS neurons exhibit a reduced capacity for growth compared to developing neurons, due in part to downregulation of growth-associated genes as development is completed. We tested the hypothesis that SnoN, an embryonically regulated transcription factor that specifies growth of the axonal compartment, can enhance growth in injured adult neurons. In vitro, SnoN overexpression in dissociated adult DRG neuronal cultures significantly enhanced neurite outgrowth. Moreover, TGF-β1, a negative regulator of SnoN, inhibited neurite outgrowth, and SnoN over-expression overcame this inhibition. We then examined whether SnoN influenced axonal regeneration in vivo: indeed, expression of a mutant form of SnoN resistant to degradation significantly enhanced axonal regeneration following cervical spinal cord injury, despite peri-lesional upregulation of TGF-β1. Thus, a developmental mechanism that specifies extension of the axonal compartment also promotes axonal regeneration after adult CNS injury.
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spelling doaj.art-0817300a011a4785ba3e3d5f4acf8a082022-12-21T17:48:21ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0188e7190610.1371/journal.pone.0071906SnoN facilitates axonal regeneration after spinal cord injury.Jiun L DoAzad BonniMark H TuszynskiAdult CNS neurons exhibit a reduced capacity for growth compared to developing neurons, due in part to downregulation of growth-associated genes as development is completed. We tested the hypothesis that SnoN, an embryonically regulated transcription factor that specifies growth of the axonal compartment, can enhance growth in injured adult neurons. In vitro, SnoN overexpression in dissociated adult DRG neuronal cultures significantly enhanced neurite outgrowth. Moreover, TGF-β1, a negative regulator of SnoN, inhibited neurite outgrowth, and SnoN over-expression overcame this inhibition. We then examined whether SnoN influenced axonal regeneration in vivo: indeed, expression of a mutant form of SnoN resistant to degradation significantly enhanced axonal regeneration following cervical spinal cord injury, despite peri-lesional upregulation of TGF-β1. Thus, a developmental mechanism that specifies extension of the axonal compartment also promotes axonal regeneration after adult CNS injury.http://europepmc.org/articles/PMC3732222?pdf=render
spellingShingle Jiun L Do
Azad Bonni
Mark H Tuszynski
SnoN facilitates axonal regeneration after spinal cord injury.
PLoS ONE
title SnoN facilitates axonal regeneration after spinal cord injury.
title_full SnoN facilitates axonal regeneration after spinal cord injury.
title_fullStr SnoN facilitates axonal regeneration after spinal cord injury.
title_full_unstemmed SnoN facilitates axonal regeneration after spinal cord injury.
title_short SnoN facilitates axonal regeneration after spinal cord injury.
title_sort snon facilitates axonal regeneration after spinal cord injury
url http://europepmc.org/articles/PMC3732222?pdf=render
work_keys_str_mv AT jiunldo snonfacilitatesaxonalregenerationafterspinalcordinjury
AT azadbonni snonfacilitatesaxonalregenerationafterspinalcordinjury
AT markhtuszynski snonfacilitatesaxonalregenerationafterspinalcordinjury