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Loss of microRNA-124 expression in neurons in the peri-lesion area in mice with spinal cord injury
Authors:Yu Zhao  Hui Zhang  Dan Zhang  Cai-yong Yu  Xiang-hui Zhao  Fang-fang Liu  Gan-lan Bian  Gong Ju  Jian Wang
Affiliation:1. Department of Anatomy, Hebei North University, Zhangjiakou, Hebei Province, China
2. Department of Stomatology, the First Hospital of Zhangjiakou, Zhangjiakou, Hebei Province, China
3. Institute of Neurosciences, the Fourth Military Medical University, Xi’an, Shaanxi Province, China
Abstract:Micro RNA-124(mi R-124) is abundantly expressed in neurons in the mammalian central nervous system, and plays critical roles in the regulation of gene expression during embryonic neurogenesis and postnatal neural differentiation. However, the expression profile of mi R-124 after spinal cord injury and the underlying regulatory mechanisms are not well understood. In the present study, we examined the expression of mi R-124 in mouse brain and spinal cord after spinal cord injury using in situ hybridization. Furthermore, the expression of mi R-124 was examined with quantitative RT-PCR at 1, 3 and 7 days after spinal cord injury. The mi R-124 expression in neurons at the site of injury was evaluated by in situ hybridization combined with Neu N immunohistochemical staining. The mi R-124 was mainly expressed in neurons throughout the brain and spinal cord. The expression of mi R-124 in neurons significantly decreased within 7 days after spinal cord injury. Some of the neurons in the peri-lesion area were Neu N+/mi R-124-. Moreover, the neurons distal to the peri-lesion site were Neu N+/mi R-124+. These findings indicate that mi R-124 expression in neurons is reduced after spinal cord injury, and may reflect the severity of spinal cord injury.
Keywords:nerve regeneration  spinal cord injury  microRNA  spinal cord  in situ hybridization  immunohistochemistry  digoxin  NeuN protein  brain  neural plasticity  repair  apoptosis  NSFC grants  neural regeneration
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