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The Journal of Neuroscience, May 1, 2002, 22(9):3553-3567
Patterns of Nogo mRNA and Protein Expression in the Developing
and Adult Rat and After CNS Lesions
Andrea B.
Huber,
Oliver
Weinmann,
Christian
Brösamle,
Thomas
Oertle, and
Martin E.
Schwab
Brain Research Institute, University of Zurich, Zurich, 8057 Switzerland, and Department of Biology, Swiss Federal Institute of
Technology, Zurich, 8057 Switzerland
Nogo-A is a neurite growth inhibitor involved in regenerative
failure and restriction of structural plasticity in the adult CNS.
Three major protein products (Nogo-A, -B, and -C) are derived from the
nogo gene. Here we describe the embryonic and postnatal expression of the three Nogo isoforms in the rat by in
situ hybridization and immunohistochemistry. Northern and
Western blot analysis indicated that Nogo-A is predominantly expressed
in the nervous system with lower levels also present in testis and
heart. In CNS myelin, confocal and immunoelectron microscopy revealed
that Nogo-A is expressed in oligodendrocyte cell bodies and processes
and localized in the innermost adaxonal and outermost myelin membranes.
Additionally, we find Nogo-A to be expressed by projection neurons, in
particular during development, and by postmitotic cells in the
developing cortex, spinal cord, and cerebellum. The expression levels
of Nogo-A/B were not changed significantly after traumatic lesions to
the cortex or spinal cord. Nogo-B showed widespread expression in the
central and peripheral nervous systems and other peripheral tissues.
Nogo-C was mainly found in skeletal muscle, but brain and heart were
also found to express this isoform. The localization of Nogo-A in
oligodendrocytes fits well with its role as a myelin-associated inhibitor of regenerative fiber growth and structural plasticity. However, expression of Nogo-A in other tissues and, in particular, in
neurons and the widespread expression of the two shorter isoforms, Nogo-B and -C, suggest that the Nogo family of proteins might have
function(s) additional to the neurite growth-inhibitory activity.
Key words:
oligodendrocyte; myelin; neurite growth inhibition; development; spinal cord injury; regeneration
Copyright © 2002 Society for Neuroscience 0270-6474/02/2293553-15$05.00/0
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