Abstract
Injured axons in mammalian peripheral nerves often regenerate successfully over long distances, in contrast to axons in the brain and spinal cord (CNS). Neurite growth-inhibitory proteins, including the recently cloned membrane protein Nogo-A, are enriched in the CNS, in particular in myelin. Nogo-A is not detectable in peripheral nerve myelin. Using regulated transgenic expression of Nogo-A in peripheral nerve Schwann cells, we show that axonal regeneration and functional recovery are impaired after a sciatic nerve crush. Nogo-A thus overrides the growth-permissive and -promoting effects of the lesioned peripheral nerve, demonstrating its in vivo potency as an inhibitor of axonal regeneration.
MeSH Terms
Animals
Axons/physiology
GAP-43 Protein/metabolism
Gene Expression Regulation
Growth Inhibitors/genetics,metabolism
HeLa Cells
Humans
Mice
Mice, Inbred C57BL
Mice, Transgenic
Myelin Proteins/genetics,metabolism
Nerve Crush
Nerve Regeneration/physiology
Nogo Proteins
Rats
Schwann Cells/metabolism
Sciatic Nerve/injuries,physiology,ultrastructure
Transgenes
Chemicals
GAP-43 Protein
Growth Inhibitors
Myelin Proteins
Nogo Proteins
RTN4 protein, human
Rtn4 protein, mouse
Rtn4 protein, rat
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Pot Caroline
Brain Research Institute, University of Zurich, and Department of Biology, Swiss Federal Institute of Technology Zurich, CH-8057 Zurich, Switzerland.
[email protected]
Simonen Marjo
Weinmann Oliver
Schnell Lisa
Christ Franziska
Stoeckle Sascha
Berger Philipp
Rülicke Thomas
Suter Ueli
Schwab Martin E
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