Quantification of N-CAM and N-cadherin expression in axotomized and crushed rat sciatic nerve

被引:42
作者
Thornton, MR
Mantovani, C
Birchall, MA
Terenghi, G
机构
[1] Univ Manchester, Blonde McIndoe Labs, Manchester M13 9PT, Lancs, England
[2] Univ Liverpool, Laryngeal Res Grp, Liverpool L69 3BX, Merseyside, England
基金
英国惠康基金;
关键词
injury; N-cadherin; NCAM; regeneration;
D O I
10.1111/j.0021-8782.2005.00369.x
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
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.
引用
收藏
页码:69 / 78
页数:10
相关论文
共 29 条
[1]   The effect of hyperbaric oxygen treatment on early regeneration of sensory axons after nerve crush in the rat [J].
Bajrovic, FF ;
Sketelj, J ;
Jug, M ;
Gril, I ;
Mekjavic, IB .
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2002, 7 (03) :141-148
[2]   IDENTIFICATION OF THE MAJOR PROTEINS THAT PROMOTE NEURONAL PROCESS OUTGROWTH ON SCHWANN-CELLS INVITRO [J].
BIXBY, JL ;
LILIEN, J ;
REICHARDT, LF .
JOURNAL OF CELL BIOLOGY, 1988, 107 (01) :353-361
[3]  
CIFUENTESDIAZ C, 1994, DEVELOPMENT, V120, P1
[4]   ALTERED EXPRESSION OF NEURONAL CELL-ADHESION MOLECULES INDUCED BY NERVE INJURY AND REPAIR [J].
DANILOFF, JK ;
LEVI, G ;
GRUMET, M ;
RIEGER, F ;
EDELMAN, GM .
JOURNAL OF CELL BIOLOGY, 1986, 103 (03) :929-945
[5]   ISOLATED GROWTH CONES STIMULATE PROLIFERATION OF CULTURED SCHWANN-CELLS [J].
DENT, EW ;
IDA, JA ;
YOSHINO, JE .
GLIA, 1992, 5 (02) :105-111
[6]   Neurite guidance molecules [J].
Doherty, P. ;
Walsh, F. S. .
CURRENT OPINION IN CELL BIOLOGY, 1989, 1 (06) :1102-1106
[7]   THE EXPRESSION OF CELL-ADHESION MOLECULES ON THE GROWTH CONES OF CHICK CUTANEOUS AND MUSCLE SENSORY NEURONS [J].
HONIG, MG ;
KUETER, J .
DEVELOPMENTAL BIOLOGY, 1995, 167 (02) :563-583
[8]  
Ide C, 1996, NEUROSCI RES, V25, P101
[9]   MYELINATED, BUT NOT UNMYELINATED AXONS, REVERSIBLY DOWN-REGULATE N-CAM IN SCHWANN-CELLS [J].
JESSEN, KR ;
MIRSKY, R ;
MORGAN, L .
JOURNAL OF NEUROCYTOLOGY, 1987, 16 (05) :681-688
[10]   Effects of FK506 on regeneration and macrophages in injured rat sciatic nerve [J].
Kvist, M ;
Danielsen, N ;
Dahlin, LB .
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2003, 8 (04) :251-259