Vaccination stimulates retinal ganglion cell regeneration in the adult optic nerve

被引:28
作者
Ellezam, B [1 ]
Bertrand, J [1 ]
Dergham, P [1 ]
McKerracher, L [1 ]
机构
[1] Univ Montreal, Dept Pathol & Biol Cellulaire, Montreal, PQ H3C 3J7, Canada
基金
加拿大健康研究院;
关键词
growth-inhibitory proteins; optic nerve crush; regeneration; cell survival; immune response; axotomy;
D O I
10.1016/S0969-9961(02)00013-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We examined whether vaccination of adult rats with spinal cord homogenate (SCH) can promote regeneration of retinal ganglion cells (RGCs) after microcrush lesion of the optic nerve. Injured animals vaccinated with SCH showed axon growth into the optic nerve and such regeneration was not observed in animals vaccinated with liver homogenate (LH). Regeneration was not a consequence of neuroprotection since our vaccine did not protect RGCs from axotomy-induced cell death. Sera of vaccinated animals were tested for antibodies against myelin-associated glycoprotein, NogoA, Nogo-66 receptor, or chondroitin sulphate proteoglycans (CSPG), but no significant levels were detected. Antibodies to myelin basic protein were present in the serum of some SCH-vaccinated animals. In culture, serum from SCH-vaccinated animals promoted RGC growth on myelin but not on CSPG. Our results show that the effect of the pro-regenerative vaccine is mediated by antibodies to SCH. However, we were not able to detect a significant immune reaction to growth inhibitory proteins, suggesting alternative mechanisms for the success of vaccination to promote regeneration. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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