Article: Optimal time point for neuronal generation of transplanted neural progenitor cells in injured Spinal cord following root avulsion

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TitleOptimal time point for neuronal generation of transplanted neural progenitor cells in injured Spinal cord following root avulsion
AuthorsSu, H2
Wu, Y3
Yuan, Q2
Guo, J1
Zhang, W2 5
Wu, W2 4
Issue Date2011
CitationCell Transplantation, 2011, v. 20 n. 2, p. 167-176 [How to Cite?]
DOI: http://dx.doi.org/10.3727/096368910X522090
AbstractRoot avulsion of the brachial plexus results in a progressive and pronounced loss of motoneurons. Cell replacement strategies have therapeutic potential in the treatment of motoneuron degenerative neurological disorders. Here, we transplanted spinal cord-derived neural progenitor cells (NPCs) into the cervical ventral horn of adult rats immediately, 2 weeks, or 6 weeks after root avulsion to determine an optimal time scale for the survival and differentiation of grafted cells. We showed that grafted NPCs survived robustly at all three time points and there was no statistical difference in survival rate. Interestingly, however, transplantation at 2 weeks postavulsion significantly increased the neuronal differentiation of transplanted NPCs compared to transplantation immediately or at 6 weeks postavulsion. Moreover, only NPCs transplanted at 2 weeks postavulsion were able to differentiate into choline acetyltransferase (ChAT)-positive neurons. Specific ELISAs and quantitative reverse transcriptase polymerase chain reaction (RT-PCR) demonstrated that expression levels of BDNF and GDNF were significantly upregulated in the ventral cord at 2 weeks postavulsion compared to immediately or at 6 weeks postavulsion. Our study suggests that the cervical ventral horn at 2 weeks postavulsion both supports neuronal differentiation and induces region-specific neuronal generation possibly because of its higher expression of BDNF and GDNF. © 2011 Cognizant Comm. Corp.
ISSN0963-6897
2011 SCImago Journal Rankings: 0.260
DOIhttp://dx.doi.org/10.3727/096368910X522090
ISI Accession Number IDWOS:000289322000003
Funding AgencyGrant Number
HKU Spinal Cord Injury Foundation
National key basic research support foundation2011CB504402
Funding Information:

This study was supported by HKU Spinal Cord Injury Foundation and National key basic research support foundation (973 project: 2011CB504402).

ReferencesReferences in Scopus
DC Field
Value
dc.contributor.authorSu, H
dc.contributor.authorWu, Y
dc.contributor.authorYuan, Q
dc.contributor.authorGuo, J
dc.contributor.authorZhang, W
dc.contributor.authorWu, W
dc.date.accessioned2012-06-26T05:58:11Z
dc.date.available2012-06-26T05:58:11Z
dc.date.issued2011
dc.description.abstractRoot avulsion of the brachial plexus results in a progressive and pronounced loss of motoneurons. Cell replacement strategies have therapeutic potential in the treatment of motoneuron degenerative neurological disorders. Here, we transplanted spinal cord-derived neural progenitor cells (NPCs) into the cervical ventral horn of adult rats immediately, 2 weeks, or 6 weeks after root avulsion to determine an optimal time scale for the survival and differentiation of grafted cells. We showed that grafted NPCs survived robustly at all three time points and there was no statistical difference in survival rate. Interestingly, however, transplantation at 2 weeks postavulsion significantly increased the neuronal differentiation of transplanted NPCs compared to transplantation immediately or at 6 weeks postavulsion. Moreover, only NPCs transplanted at 2 weeks postavulsion were able to differentiate into choline acetyltransferase (ChAT)-positive neurons. Specific ELISAs and quantitative reverse transcriptase polymerase chain reaction (RT-PCR) demonstrated that expression levels of BDNF and GDNF were significantly upregulated in the ventral cord at 2 weeks postavulsion compared to immediately or at 6 weeks postavulsion. Our study suggests that the cervical ventral horn at 2 weeks postavulsion both supports neuronal differentiation and induces region-specific neuronal generation possibly because of its higher expression of BDNF and GDNF. © 2011 Cognizant Comm. Corp.
dc.description.natureLink_to_subscribed_fulltext
dc.identifier.citationCell Transplantation, 2011, v. 20 n. 2, p. 167-176 [How to Cite?]
DOI: http://dx.doi.org/10.3727/096368910X522090
dc.identifier.citeulike9121753
dc.identifier.doihttp://dx.doi.org/10.3727/096368910X522090
dc.identifier.epage176
dc.identifier.isiWOS:000289322000003
Funding AgencyGrant Number
HKU Spinal Cord Injury Foundation
National key basic research support foundation2011CB504402
Funding Information:

This study was supported by HKU Spinal Cord Injury Foundation and National key basic research support foundation (973 project: 2011CB504402).

dc.identifier.issn0963-6897
2011 SCImago Journal Rankings: 0.260
dc.identifier.issue2
dc.identifier.pmid20719091
dc.identifier.scopuseid_2-s2.0-79955395422
dc.identifier.spage167
dc.identifier.urihttp://hdl.handle.net/10722/149762
dc.identifier.volume20
dc.languageeng
dc.publisher.placeUnited States
dc.relation.ispartofCell Transplantation
dc.relation.referencesReferences in Scopus
dc.subject.meshAnimals
dc.subject.meshAnterior Horn Cells - Pathology
dc.subject.meshBrain-Derived Neurotrophic Factor - Metabolism
dc.subject.meshCell Differentiation
dc.subject.meshCells, Cultured
dc.subject.meshCholine O-Acetyltransferase - Metabolism
dc.subject.meshFemale
dc.subject.meshGlial Cell Line-Derived Neurotrophic Factor - Metabolism
dc.subject.meshNeural Stem Cells - Transplantation
dc.subject.meshNeurons - Cytology - Enzymology
dc.subject.meshRadiculopathy - Complications - Pathology - Therapy
dc.subject.meshRats
dc.subject.meshRats, Sprague-Dawley
dc.subject.meshSpinal Cord Injuries - Complications - Therapy
dc.subject.meshStem Cell Transplantation
dc.subject.meshTime Factors
dc.titleOptimal time point for neuronal generation of transplanted neural progenitor cells in injured Spinal cord following root avulsion
dc.typeArticle
Author Affiliations
  1. Southern Medical University
  2. The University of Hong Kong Li Ka Shing Faculty of Medicine
  3. UCL Institute of Child Health
  4. Jinan University
  5. First Affiliated Hospital of Fujian Medical University