Suppr超能文献

[p75神经营养因子受体基因敲除对小鼠面神经挤压伤后再生的影响]

[Influence of p75 neurotrophin receptor knockout on the regeneration of facial nerves after crush injury in mouse].

作者信息

Zhang Feng-He, Huang Ping, Yang Pi-Shan, Zhang Xue

机构信息

Dept. of Oral and Maxillofacial Surgery, School of Stomatology, Shandong University, Jinan 250012, China.

出版信息

Hua Xi Kou Qiang Yi Xue Za Zhi. 2010 Feb;28(1):95-8.

Abstract

OBJECTIVE

To investigate the role of p75 neurotrophin receptor (p75NTR) in the regeneration of facial nerve crush injury.

METHODS

In p75NTR knockout mice and wild type mice, the regenerating fibres in the facial nerve were also labelled by an anterograde tracer cholera toxin B (CTB). The next day after injury of facial nerve, CTB was injected into the trunk of the nerve in the proximal side of the crush, and then anterograde tracing and immunohistochemistry were used to examine the regeneration of axons after facial nerve crush injury. In p75NTR knockout mice and wild type mice, the facial nerves on one side were crushed and regenerating neurons in the facial nerve nucleus were labelled by Fast Blue. The facial nerve trunk was cut in the bifurcated region in the 4th day after injury and the stump was inserted into a small polymer tube containing Fast Blue. Retrograde tracing and labling motoneuron counting were used to examine the survival of motoneurons in the facial nerve nucleus after facial nerve crush injury.

RESULTS

The results showed that the axonal growth of injured axons in the facial nerve of p75NTR knockout mice was significantly retarded. The number of regenerated neurons in the facial nerve nucleus in p75NTR knockout mice was significantly reduced (P < 0.05). Immunohistochemical staining of regenerating axons also showed the reduction in nerve regeneration in p75NTR knockout mice (P < 0.01).

CONCLUSION

p75NTR plays an important role in the regeneration of injured peripheral nerves after injury.

摘要

目的

探讨p75神经营养因子受体(p75NTR)在面神经挤压伤再生中的作用。

方法

在p75NTR基因敲除小鼠和野生型小鼠中,面神经中的再生纤维也用顺行示踪剂霍乱毒素B(CTB)标记。面神经损伤后第二天,将CTB注入挤压近端的神经干,然后用顺行示踪和免疫组织化学方法检测面神经挤压伤后轴突的再生情况。在p75NTR基因敲除小鼠和野生型小鼠中,一侧面神经被挤压,面神经核中的再生神经元用快蓝标记。在损伤后第4天,在面神经分叉区域切断面神经干,将残端插入含有快蓝的小聚合物管中。用逆行示踪和标记运动神经元计数法检测面神经挤压伤后面神经核中运动神经元的存活情况。

结果

结果显示,p75NTR基因敲除小鼠面神经损伤轴突的轴突生长明显延迟。p75NTR基因敲除小鼠面神经核中再生神经元的数量明显减少(P<0.05)。再生轴突的免疫组织化学染色也显示p75NTR基因敲除小鼠神经再生减少(P<0.01)。

结论

p75NTR在损伤后外周神经损伤的再生中起重要作用。

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