Zhao Yu, Zhang Hui, Zhang Dan, Yu Cai-Yong, Zhao Xiang-Hui, Liu Fang-Fang, Bian Gan-Lan, Ju Gong, Wang Jian
Department of Anatomy, Hebei North University, Zhangjiakou, Hebei Province, China.
Department of Stomatology, the First Hospital of Zhangjiakou, Zhangjiakou, Hebei Province, China.
Neural Regen Res. 2015 Jul;10(7):1147-52. doi: 10.4103/1673-5374.156983.
MicroRNA-124 (miR-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 miR-124 after spinal cord injury and the underlying regulatory mechanisms are not well understood. In the present study, we examined the expression of miR-124 in mouse brain and spinal cord after spinal cord injury using in situ hybridization. Furthermore, the expression of miR-124 was examined with quantitative RT-PCR at 1, 3 and 7 days after spinal cord injury. The miR-124 expression in neurons at the site of injury was evaluated by in situ hybridization combined with NeuN immunohistochemical staining. The miR-124 was mainly expressed in neurons throughout the brain and spinal cord. The expression of miR-124 in neurons significantly decreased within 7 days after spinal cord injury. Some of the neurons in the peri-lesion area were NeuN(+)/miR-124(-). Moreover, the neurons distal to the peri-lesion site were NeuN(+)/miR-124(+). These findings indicate that miR-124 expression in neurons is reduced after spinal cord injury, and may reflect the severity of spinal cord injury.
微小RNA-124(miR-124)在哺乳动物中枢神经系统的神经元中大量表达,并在胚胎神经发生和出生后神经分化过程中的基因表达调控中发挥关键作用。然而,脊髓损伤后miR-124的表达谱及其潜在调控机制尚不清楚。在本研究中,我们使用原位杂交技术检测了脊髓损伤后小鼠脑和脊髓中miR-124的表达。此外,在脊髓损伤后1天、3天和7天,用定量逆转录-聚合酶链反应检测miR-124的表达。通过原位杂交结合NeuN免疫组化染色评估损伤部位神经元中miR-124的表达。miR-124主要在整个脑和脊髓的神经元中表达。脊髓损伤后7天内,神经元中miR-124的表达显著降低。损伤周围区域的一些神经元为NeuN(+)/miR-124(-)。此外,损伤周围部位远端的神经元为NeuN(+)/miR-124(+)。这些发现表明,脊髓损伤后神经元中miR-124的表达降低,可能反映脊髓损伤的严重程度。