Suppr超能文献

再生哺乳动物视神经中的交叉特异性

Chiasmatic specificity in the regenerating mammalian optic nerve.

作者信息

MacLaren R E, Taylor J S

机构信息

Department of Human Anatomy, University of Oxford, United Kingdom.

出版信息

Exp Neurol. 1997 Oct;147(2):279-86. doi: 10.1006/exnr.1997.6620.

Abstract

The mammalian central nervous system is capable of regenerating; however, there is no evidence that the regenerating axons can navigate along their normal pathways and reestablish topographically organized projections: essential for functional return of vision. Here retinal ganglion cells in the opossum Monodelphis were birthdated with tritiated thymidine on the sixth postnatal day (P6), before being lesioned in the temporal retina at P8. Retrograde tracing with horseradish peroxidase injected into the ipsilateral optic tract at P24 showed that the temporal crescent had reformed behind the retinal lesion. By comparisons of cell and thymidine counts from lesioned and control regions of retina, it was estimated that about 40% of the normal number of ganglion cells are able to regenerate into the ipsilateral optic tract following a lesion in the temporal retina at P8. A clear line of decussation (separation of ipsilateral and contralateral projections) reformed in the lesioned temporal retina and regenerating ganglion cells labeled with DiI were turned at appropriate points on passing through the optic chiasm. This is evidence of chiasmatic specificity with regard to lesioned retinal ganglion cells regenerating into the ipsilateral optic tract.

摘要

哺乳动物的中枢神经系统具有再生能力;然而,没有证据表明再生的轴突能够沿着其正常路径导航并重新建立拓扑组织化的投射:这对视觉功能恢复至关重要。在这里,负鼠(Monodelphis)的视网膜神经节细胞在出生后第6天(P6)用氚化胸腺嘧啶核苷进行标记,然后在P8时颞侧视网膜受到损伤。在P24时将辣根过氧化物酶注入同侧视束进行逆行追踪,结果显示在视网膜损伤后方形成了颞侧新月形。通过比较损伤视网膜区域和对照区域的细胞和胸腺嘧啶核苷计数,估计在P8时颞侧视网膜损伤后,约40%的正常数量神经节细胞能够再生进入同侧视束。在损伤的颞侧视网膜中重新形成了一条清晰的交叉线(同侧和对侧投射的分离),用DiI标记的再生神经节细胞在穿过视交叉的适当位置发生转向。这证明了损伤的视网膜神经节细胞再生进入同侧视束时视交叉具有特异性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验