Loss of microRNA-124 expression in neurons in the peri-lesion area in mice with spinal cord injury |
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Authors: | Yu Zhao Hui Zhang Dan Zhang Cai-yong Yu Xiang-hui Zhao Fang-fang Liu Gan-lan Bian Gong Ju Jian Wang |
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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 |
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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. |
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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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