Source:http://linkedlifedata.com/resource/pubmed/id/16941122
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2006-11-28
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pubmed:abstractText |
Adult neural progenitor cells (NPC) co-grafted with fibroblasts replace cystic lesion defects and promote cell-contact-mediated axonal regeneration in the acutely injured spinal cord. Fibroblasts are required as a platform to maintain NPC within the lesion; however, they are suspected to create an inhospitable milieu for regenerating central nervous system (CNS) axons. Therefore, we thought to replace fibroblasts by primary Schwann cells, which might serve as a superior scaffold to maintain NPC within the lesion and might further enhance axon regrowth and remyelination following spinal cord injury. Adult rats underwent a cervical dorsal column transection immediately followed by transplantation of either NPC/Schwann cell or NPC/Schwann cell/fibroblast co-grafts. Animals receiving Schwann cell or fibroblast grafts alone, or Schwann cell/fibroblast co-grafts served as controls. At 3 weeks after injury/transplantation, histological analysis revealed that only fibroblast-containing grafts were able to replace the cystic lesion defect. In both co-cultures and co-grafts, Schwann cells and NPC were segregated. Almost all NPC migrated out of the graft into the adjacent host spinal cord. As a consequence, only peripheral-type myelin, but no CNS-type myelin, was detected within co-grafts containing NPC/Schwann cells. Corticospinal axon regeneration into Schwann-cell-containing co-grafts was reduced. Taken together, Schwann cells within NPC grafts contribute to remyelination. However, Schwann cells fail as a supporting platform to maintain NPC within the graft and impair CNS axon regeneration; this makes them an unfavorable candidate to support/augment NPC grafts following spinal cord injury.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0302-766X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
327
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1-13
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pubmed:meshHeading |
pubmed-meshheading:16941122-Animals,
pubmed-meshheading:16941122-Axons,
pubmed-meshheading:16941122-Cell Movement,
pubmed-meshheading:16941122-Cell Survival,
pubmed-meshheading:16941122-Coculture Techniques,
pubmed-meshheading:16941122-Cysts,
pubmed-meshheading:16941122-Disease Models, Animal,
pubmed-meshheading:16941122-Female,
pubmed-meshheading:16941122-Fluorescent Antibody Technique, Indirect,
pubmed-meshheading:16941122-Myelin Sheath,
pubmed-meshheading:16941122-Nerve Regeneration,
pubmed-meshheading:16941122-Neurons,
pubmed-meshheading:16941122-Rats,
pubmed-meshheading:16941122-Rats, Inbred F344,
pubmed-meshheading:16941122-Schwann Cells,
pubmed-meshheading:16941122-Spinal Cord Injuries,
pubmed-meshheading:16941122-Stem Cell Transplantation,
pubmed-meshheading:16941122-Stem Cells
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pubmed:year |
2007
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pubmed:articleTitle |
Failure of Schwann cells as supporting cells for adult neural progenitor cell grafts in the acutely injured spinal cord.
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pubmed:affiliation |
Department of Neurology, University of Regensburg, Universitätsstrasse 84, 93053 Regensburg, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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