Attempted endogenous tissue repair following experimental spinal cord injury in the rat: involvement of cell adhesion molecules L1 and NCAM?

It is widely accepted that the devastating consequences of spinal cord injury are due to the failure of lesioned CNS axons to regenerate. The current study of the spontaneous tissue repair processes following dorsal hemisection of the adult rat spinal cord demonstrates a phase of rapid and substanti...

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Published inThe European journal of neuroscience Vol. 12; no. 9; pp. 3224 - 3238
Main Authors Brook, Gary A., Houweling, Diane A., Gieling, Roben G., Hermanns, Thomas, Joosten, Elbert A. J., Bär, Dop P. R., Gispen, Willem-Hendrik, Schmitt, Andreas B., Leprince, P., Noth, Johannes, Nacimiento, Wilhelm
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Ltd 01.09.2000
Wiley Subscription Services, Inc
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Summary:It is widely accepted that the devastating consequences of spinal cord injury are due to the failure of lesioned CNS axons to regenerate. The current study of the spontaneous tissue repair processes following dorsal hemisection of the adult rat spinal cord demonstrates a phase of rapid and substantial nerve fibre in‐growth into the lesion that was derived largely from both rostral and caudal spinal tissues. The response was characterized by increasing numbers of axons traversing the clearly defined interface between the lesion and the adjacent intact spinal cord, beginning by 5 days post operation (p.o.). Having penetrated the lesion, axons became associated with a framework of NGFr‐positive non‐neuronal cells (Schwann cells and leptomeningeal cells). Surprisingly few of these axons were derived from CGRP‐ or SP‐immunoreactive dorsal root ganglion neurons. At the longest survival time (56 days p.o.), there was a marked shift in the overall orientation of fibres from a largely rostro‐caudal to a dorso‐ventral axis. Attempts to identify which recognition molecules may be important for these re‐organizational processes during attempted tissue repair demonstrated the widespread and intense expression of the cell adhesion molecules (CAM) L1 and N‐CAM. Double immunofluorescence suggested that both Schwann cells and leptomeningeal cells contributed to the pattern of CAM expression associated with the cellular framework within the lesion.
Bibliography:ark:/67375/WNG-HC44LBR9-J
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ArticleID:EJN228
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ISSN:0953-816X
1460-9568
DOI:10.1046/j.1460-9568.2000.00228.x