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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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 |
work_keys_str_mv |
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