| Literature DB >> 31991126 |
Muhua Lai1, Mengjie Pan2, Longjiao Ge3, Jingmin Liu1, Junyao Deng1, Xianghai Wang1, Lixia Li1, Jinkun Wen1, Dandan Tan1, Haowen Zhang1, Xiaofang Hu1, Lanya Fu1, Yizhou Xu1, Zhenlin Li1, Xiaozhong Qiu4, Gong Chen5, Jiasong Guo6.
Abstract
Neurogenic differentiation 1 (NeuroD1) is mainlyexpressed in developing neurons where it plays critical roles in neuronal maturation and neurite elongation. The potential role and mechanism of NeuroD1 in adult axonal regeneration is not clear. The present study used synapsin (SYN) Cre and AAV9-Flex vectors to conditionally overexpress NeuroD1 in adult spinal neurons and found that NeuroD1 overexpression significantly accelerated axonal regeneration and functional recovery after sciatic nerve injury. Further in vitro and in vivo experiments suggested that the mechanism of NeuroD1 promotion on axonal regeneration was related to its regulation of the expression of neurotrophin BDNF and its receptor TrkB as well as a microtubule severing protein spastin.Entities:
Keywords: Axonal regeneration; BDNF; NeuroD1; Neuron; Sciatic nerve injury; Spastin; Spinal cord; TrkB
Year: 2020 PMID: 31991126 DOI: 10.1016/j.expneurol.2020.113215
Source DB: PubMed Journal: Exp Neurol ISSN: 0014-4886 Impact factor: 5.330