Peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.

Trauma to the spinal cord and brain can result in irreparable loss of function. This failure of recovery is in part due to inhibition of axon regeneration by myelin and chondroitin sulfate proteoglycans (CSPGs). Peripheral nervous system (PNS) neurons exhibit increased regenerative ability compared...

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Main Authors: William J Buchser, Robin P Smith, Jose R Pardinas, Candace L Haddox, Thomas Hutson, Lawrence Moon, Stanley R Hoffman, John L Bixby, Vance P Lemmon
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3368946?pdf=render
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spelling doaj-823612981fad42a38e72e9ac81678c412020-11-25T02:15:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0176e3810110.1371/journal.pone.0038101Peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.William J BuchserRobin P SmithJose R PardinasCandace L HaddoxThomas HutsonLawrence MoonStanley R HoffmanJohn L BixbyVance P LemmonTrauma to the spinal cord and brain can result in irreparable loss of function. This failure of recovery is in part due to inhibition of axon regeneration by myelin and chondroitin sulfate proteoglycans (CSPGs). Peripheral nervous system (PNS) neurons exhibit increased regenerative ability compared to central nervous system neurons, even in the presence of inhibitory environments. Previously, we identified over a thousand genes differentially expressed in PNS neurons relative to CNS neurons. These genes represent intrinsic differences that may account for the PNS's enhanced regenerative ability. Cerebellar neurons were transfected with cDNAs for each of these PNS genes to assess their ability to enhance neurite growth on inhibitory (CSPG) or permissive (laminin) substrates. Using high content analysis, we evaluated the phenotypic profile of each neuron to extract meaningful data for over 1100 genes. Several known growth associated proteins potentiated neurite growth on laminin. Most interestingly, novel genes were identified that promoted neurite growth on CSPGs (GPX3, EIF2B5, RBMX). Bioinformatic approaches also uncovered a number of novel gene families that altered neurite growth of CNS neurons.http://europepmc.org/articles/PMC3368946?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author William J Buchser
Robin P Smith
Jose R Pardinas
Candace L Haddox
Thomas Hutson
Lawrence Moon
Stanley R Hoffman
John L Bixby
Vance P Lemmon
spellingShingle William J Buchser
Robin P Smith
Jose R Pardinas
Candace L Haddox
Thomas Hutson
Lawrence Moon
Stanley R Hoffman
John L Bixby
Vance P Lemmon
Peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.
PLoS ONE
author_facet William J Buchser
Robin P Smith
Jose R Pardinas
Candace L Haddox
Thomas Hutson
Lawrence Moon
Stanley R Hoffman
John L Bixby
Vance P Lemmon
author_sort William J Buchser
title Peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.
title_short Peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.
title_full Peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.
title_fullStr Peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.
title_full_unstemmed Peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.
title_sort peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Trauma to the spinal cord and brain can result in irreparable loss of function. This failure of recovery is in part due to inhibition of axon regeneration by myelin and chondroitin sulfate proteoglycans (CSPGs). Peripheral nervous system (PNS) neurons exhibit increased regenerative ability compared to central nervous system neurons, even in the presence of inhibitory environments. Previously, we identified over a thousand genes differentially expressed in PNS neurons relative to CNS neurons. These genes represent intrinsic differences that may account for the PNS's enhanced regenerative ability. Cerebellar neurons were transfected with cDNAs for each of these PNS genes to assess their ability to enhance neurite growth on inhibitory (CSPG) or permissive (laminin) substrates. Using high content analysis, we evaluated the phenotypic profile of each neuron to extract meaningful data for over 1100 genes. Several known growth associated proteins potentiated neurite growth on laminin. Most interestingly, novel genes were identified that promoted neurite growth on CSPGs (GPX3, EIF2B5, RBMX). Bioinformatic approaches also uncovered a number of novel gene families that altered neurite growth of CNS neurons.
url http://europepmc.org/articles/PMC3368946?pdf=render
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