Increased NCAM-180 immunoreactivity and maintenance of L1 immunoreactivity in injured optic fibers of adult mice

被引:17
作者
Becker, CG [1 ]
Becker, T
Meyer, RL
机构
[1] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92697 USA
[2] Univ Hamburg, Zentrum Mol Neurobiol, D-20246 Hamburg, Germany
关键词
polysialic acid; regeneration; CNS; retinal ganglion cells; cell adhesion molecules; immunoglobulin superfamily;
D O I
10.1006/exnr.2001.7657
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The injury related expression of two axon-growth promoting cell adhesion molecules (CAMs), NCAM-180 which is developmentally downregulated and L1 which is regionally restricted, were compared in optic fibers in the adult mouse. The neuron-specific isoform of NCAM (NCAM-180) is present at very low levels in unlesioned adult optic axone. At 7 days after nerve crush, immunoreactivity was strongly and uniformly increased in optic axons within the nerve and throughout retina. Reactivity in surviving axons had returned to control levels at 4 weeks. To induce regrowth of adult retinal ganglion cell axone retinal explants were placed in culture. Strong NCAM-180 staining was observed on these regenerating optic axone. The neuronal cell adhesion molecule L1 is restricted to retina and to the unmyelinated segment of the optic nerve near the optic nerve head in unlesioned adult animals. Following nerve crush, L1 immunoreactivity was retained within retina and proximal nerve and novel staining was detected in the more distal segment of the optic nerve up to the lesion site where it persisted for at least eight months. The capacity of optic fibers to show increased NCAM-180 immunoreactivity and maintain L1 expression after a lesion may explain why these fibers exhibit relatively good potential for regeneration. (C) 2001 Academic Press.
引用
收藏
页码:438 / 448
页数:11
相关论文
共 66 条
[21]  
Buffo A, 1997, J NEUROSCI, V17, P8778
[22]   Spontaneous axonal regeneration after optic nerve injury in adult rat [J].
Campbell, G ;
Holt, JKL ;
Shotton, HR ;
Anderson, PN ;
Bavetta, S ;
Lieberman, AR .
NEUROREPORT, 1999, 10 (18) :3955-3960
[23]   Axonal regeneration from CNS neurons in the cerebellum and brainstem of adult rats: Correlation with the patterns of expression and distribution of messenger RNAs for L1, CHL1, c-jun and growth-associated protein-43 [J].
Chaisuksunt, V ;
Zhang, Y ;
Anderson, PN ;
Campbell, G ;
Vaudano, E ;
Schachner, M ;
Lieberman, AR .
NEUROSCIENCE, 2000, 100 (01) :87-108
[24]   Regeneration of adult axons in white matter tracts of the central nervous system [J].
Davies, SJA ;
Fitch, MT ;
Memberg, SP ;
Hall, AK ;
Raisman, G ;
Silver, J .
NATURE, 1997, 390 (6661) :680-683
[25]  
Delius JAM, 1997, J NEUROSCI RES, V49, P255, DOI 10.1002/(SICI)1097-4547(19970801)49:3<255::AID-JNR1>3.0.CO
[26]  
2-B
[27]  
DEZERWA M, 1996, ANAT REC, V246, P114
[28]   NEURITE OUTGROWTH IN RESPONSE TO TRANSFECTED N-CAM CHANGES DURING DEVELOPMENT AND IS MODULATED BY POLYSIALIC ACID [J].
DOHERTY, P ;
COHEN, J ;
WALSH, FS .
NEURON, 1990, 5 (02) :209-219
[29]   EXPRESSION OF THE GROWTH-ASSOCIATED PROTEIN GAP-43 IN ADULT-RAT RETINAL GANGLION-CELLS FOLLOWING AXON INJURY [J].
DOSTER, SK ;
LOZANO, AM ;
AGUAYO, AJ ;
WILLARD, MB .
NEURON, 1991, 6 (04) :635-647
[30]  
Dusart I, 1999, J COMP NEUROL, V408, P399