Wang Hongkui, Zhu Hui, Guo Qi, Qian Tianmei, Zhang Ping, Li Shiying, Xue Chengbin, Gu Xiaosong
Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, China.
Jiangsu Clinical Medicine Center of Tissue Engineering and Nerve Injury Repair, Research Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, China.
Front Cell Neurosci. 2017 Oct 11;11:323. doi: 10.3389/fncel.2017.00323. eCollection 2017.
Peripheral nervous system owns the ability of self-regeneration, mainly in its regenerative microenvironment including vascular network reconstruction. More recently, more attentions have been given to the close relationship between tissue regeneration and angiogenesis. To explore the overlap of molecular mechanisms and key regulation molecules between peripheral nerve regeneration and angiogenesis post peripheral nerve injury, integrative and bioinformatic analysis was carried out for microarray data of proximal stumps after sciatic nerve transection in SD rats. Nerve regeneration and angiogenesis were activated at 1 day immediately after sciatic nerve transection simultaneously. The more obvious changes of transcription regulators and canonical pathways suggested a phase transition between 1 and 4 days of both nerve regeneration and angiogenesis after sciatic nerve transection. Furthermore, 16 differentially expressed genes participated in significant biological processes of both nerve regeneration and angiogenesis, a few of which were validated by qPCR and immunofluorescent staining. It was demonstrated that STAT3, EPHB3, and Cdc42 co-expressed in Schwann cells and vascular endothelial cells to play a key role in regulation of nerve regeneration and angiogenesis simultaneously response to sciatic nerve transection. We provide a framework for understanding biological processes and precise molecular correlations between peripheral nerve regeneration and angiogenesis after peripheral nerve transection. Our work serves as an experimental basis and a valuable resource to further understand molecular mechanisms that define nerve injury-induced micro-environmental variation for achieving desired peripheral nerve regeneration.
外周神经系统具有自我再生能力,主要体现在其再生微环境中,包括血管网络重建。最近,组织再生与血管生成之间的密切关系受到了更多关注。为了探究外周神经损伤后外周神经再生与血管生成之间分子机制和关键调控分子的重叠情况,对SD大鼠坐骨神经横断后近端残端的微阵列数据进行了整合和生物信息学分析。坐骨神经横断后1天,神经再生和血管生成同时被激活。转录调节因子和经典途径更明显的变化表明,坐骨神经横断后1至4天,神经再生和血管生成均发生了阶段转变。此外,16个差异表达基因参与了神经再生和血管生成的重要生物学过程,其中一些通过qPCR和免疫荧光染色得到了验证。结果表明,STAT3、EPHB3和Cdc42在雪旺细胞和血管内皮细胞中共同表达,在坐骨神经横断后同时调节神经再生和血管生成中起关键作用。我们提供了一个框架,用于理解外周神经横断后外周神经再生与血管生成之间的生物学过程和精确分子关联。我们的工作为进一步理解定义神经损伤诱导的微环境变化以实现理想的外周神经再生的分子机制提供了实验基础和宝贵资源。