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Neurotrophins 3 and 4 differentially regulate NCAM, L1 and N‐cadherin expression during peripheral nerve regeneration
Author(s) -
Thornton Martin R.,
Shawcross Susan G.,
Mantovani Cristina,
Kingham Paul J.,
Birchall Martin A.,
Terenghi Giorgio
Publication year - 2008
Publication title -
biotechnology and applied biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.468
H-Index - 70
eISSN - 1470-8744
pISSN - 0885-4513
DOI - 10.1042/ba20070040
Subject(s) - neural cell adhesion molecule , cell adhesion molecule , cadherin , regeneration (biology) , axon , neurotrophin , neurotrophin 3 , sciatic nerve , microbiology and biotechnology , biology , cell adhesion , anatomy , neurotrophic factors , cell , brain derived neurotrophic factor , receptor , biochemistry
The addition of NT‐3 (neurotrophin 3) or NT‐4 to injured nerves improves their regeneration potential and may aid axon guidance. It is not well defined whether NTs (neurotrophins) influence other elements, such as the cell‐adhesion molecules, which promote nerve guidance and regeneration. Using poly‐3‐hydroxybutyrate conduits, we applied either NT‐3 or NT‐4 to axotomized rat sciatic nerves and monitored nerve regeneration and cell‐adhesion molecule expression. Regenerating nerves were stained with antibodies against NCAM (neural cell‐adhesion molecule) and N‐cadherin 2 weeks after injury and staining intensity was quantified. NCAM, N‐cadherin and L1 (L1 cell‐adhesion molecule) transcription was measured in the proximal and distal stumps and ipsilateral DRG (dorsal root ganglia) (fourth and fifth DRG) using RT (reverse transcriptase)–PCR. Both NT‐3 and NT‐4 increased NCAM and L1 transcript levels in the DRG of axotomized nerves. This is reflected in the increased NCAM expression at the proximal stump and regeneration front. Increased levels of NCAM were also observed in the distal stump. NT‐4 administration increased N‐cadherin levels proximal to the injury, but not distally. Following NT‐3 administration, N‐cadherin expression decreased in proximal and distal stumps compared with the control. In conclusion, NTs differentially alter adhesion molecule expression in regenerating nerves and transcription in the corresponding DRG, although these changes in expression do not alter NT‐enhanced regeneration. Thus we propose that retrograde transport of the NTs to the DRG affects adhesion molecule transcription, reflected by protein expression in peripheral nerve axons.