Premium
NT‐3 promotes growth of lesioned adult rat sensory axons ascending in the dorsal columns of the spinal cord
Author(s) -
Bradbury Elizabeth J.,
Khemani Sameer,
Von R .,
King .,
Priestley John V.,
McMahon Stephen B.
Publication year - 1999
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1046/j.1460-9568.1999.00809.x
Subject(s) - spinal cord , lesion , sprouting , anatomy , regeneration (biology) , glial cell line derived neurotrophic factor , neuroscience , neurotrophic factors , neurotrophin , biology , pathology , medicine , microbiology and biotechnology , receptor , biochemistry , botany
Abstract The regeneration capacity of spinal cord axons is severely limited. Recently, much attention has focused on promoting regeneration of descending spinal cord pathways, but little is known about the regenerative capacity of ascending axons. Here we have assessed the ability of neurotrophic factors to promote regeneration of sensory neurons whose central axons ascend in the dorsal columns. The dorsal columns of adult rats were crushed and either brain‐derived neurotrophic factor (BDNF), glial cell line‐derived neurotrophic factor (GDNF), neurotrophin‐3 (NT‐3) or a vehicle solution was delivered continuously to the lesion site for 4 weeks. Transganglionic labelling with cholera toxin β subunit (CTB) was used to selectively label large myelinated Aβ fibres. In lesioned rats treated with vehicle, CTB‐labelled fibres were observed ascending in the gracile fasciculus, but these stopped abruptly at the lesion site, with no evidence of sprouting or growth into lesioned tissue. No CTB‐labelled terminals were observed in the gracile nucleus, indicating that the lesion successfully severed all ascending dorsal column axons. Treatment with BDNF did not promote axonal regeneration. In GDNF‐treated rats fibres grew around cavities in caudal degenerated tissue but did not approach the lesion epicentre. NT‐3, in contrast, had a striking effect on promoting growth of lesioned dorsal column axons with an abundance of fibre sprouting apparent at the lesion site, and many fibres extending into and beyond the lesion epicentre. Quantification of fibre growth confirmed that only in NT‐3‐treated rats did fibres grow into the crush site and beyond. No evidence of terminal staining in the gracile nucleus was apparent following any treatment. Thus, although NT‐3 promotes extensive growth of lesioned axons, other factors may be required for complete regeneration of these long ascending projections back to the dorsal column nuclei. The intrathecal delivery of NT‐3 or other neurotrophic molecules has obvious advantages in clinical applications, as we show for the first time that dorsal column axonal regeneration can be achieved without the use of graft implantation or nerve lesions.