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Positioned to inhibit: Netrin‐1 and netrin receptor expression after spinal cord injury
Author(s) -
Manitt Colleen,
Wang David,
Kennedy Timothy E.,
Howland Dena R.
Publication year - 2006
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.21070
Subject(s) - netrin , axon , lesion , myelin , spinal cord , spinal cord injury , glial scar , biology , oligodendrocyte , axon guidance , central nervous system , neuroscience , pathology , anatomy , medicine
Netrin‐1 regulates axon extension during embryonic development and is expressed by neurons and myelinating oligodendrocytes in the adult CNS. To investigate the potential role of netrin‐1 after spinal cord injury, we examined the expression of netrin‐1 and netrin receptors after sagittal myelotomy in adult rats. This lesion targets spinal commissural projections, which respond to netrin‐1 during development. Netrin‐1 mRNA and protein levels were dramatically reduced at the site of injury and reduced expression persisted for at least 7 months. Neither netrin‐1 protein nor mRNA was associated with the glial scar, but netrin‐1 was expressed by neurons and oligodendrocytes immediately adjacent to the lesion. The post‐injury distribution detected is similar to that reported for myelin‐associated inhibitors of axon regeneration, such as Nogo, and is distinct from the distribution of inhibitors associated with a glial scar. DCC and UNC‐5 homologue (UNC5H) expression also was reduced after injury. Although UNC5H levels recovered, DCC expression at the site of injury remained ∼50% of pre‐injury values at 7 months. Increased UNC5H immunoreactivity was associated with fibers in the superficial layers of the dorsal horn and in fibers located in white matter adjacent to the lesion. The dominant expression of UNC5H on axons and neurons in the spinal cord after injury and the persistent expression of netrin‐1 by oligodendrocytes surrounding the lesion are consistent with the hypothesis that netrin‐1 is a myelin‐associated inhibitor of axonal regeneration after spinal cord injury. © 2006 Wiley‐Liss, Inc.