Abstract :
Adhesion molecules are important in supporting axonal regeneration. Qualitative studies have described increased
expression of neural cell adhesion molecule (NCAM) and N-cadherin in models of nerve injury allowing active
regeneration. In this study we have used quantitative immunohistochemistry to compare expression of NCAM and
N-cadherin after nerve injury either with active regeneration (crush) into the distal stump or without (axotomy and
capping). Quantification was performed 15 days after axotomy in proximal and distal stumps. Quantification after
crush either proximal, distal or within the crushed area was performed at 2, 7, 15 and 30 days after injury. Axotomy
induced increases in expression in proximal stumps between two and three times those in uninjured nerves for both
molecules. In distal stumps, N-cadherin levels increased seven-fold, yet NCAM levels did not exceed control values.
After crush, NCAM immunoreactivity increased in the crushed area and distal stump in contrast to axotomy and
NCAM-positive axons co-localized with PGP9.5. N-cadherin levels in the distal stump increased above control levels,
but the magnitude of the increase seen after crush was different to those seen after axotomy. In conclusion,
increased expression of adhesion molecules, particularly NCAM, in the distal stump of injured nerves is dependent
upon the presence of regenerating axons
Keywords :
Injury , N-cadherin , NCAM , regeneration