Xu Yong, An Bao-Yan, Xi Xiao-Bing, Li Zhong-Wei, Li Fei-Yue
Shanghai Traumatology and Orthopedics Research Institute, Shanghai 200020, China; Department of Traumatology, Ruijin Hospital, Shanghai Jiaotong University School of Medcine, Shanghai 200025, China.
Department of Infectious Diseases, Ruijin Hospital, Shanghai Jiaotong University School of Medcine, Shanghai 200025, China.
Brain Res Bull. 2016 Mar;121:233-40. doi: 10.1016/j.brainresbull.2016.01.011. Epub 2016 Jan 23.
For the purpose of an early identification of intervention targets for acute spinal cord injury (ASCI), we investigated the changes in expression levels of microRNA-9 (miR-9) and MCPIP1 in rat ASCI model.
A total of 108 healthy rats were randomly divided into non-ASCI group (n=18) and five ASCI groups, 6h, 12h, 24h, 3 days and 7 days, representing the experimental time points following ASCI (n=18 per group). Hematoxylin and eosin (HE) staining was used to assess the ASCI damage, and quantitative real-time PCR (qRT-PCR) and in situ hybridization (ISH) were employed for the detection of miR-9 and MCPIP1 mRNA expression.
HE staining results showed normal neuronal morphology in the non-ASCI group, but spinal cord tissue at 6h after ASCI showed developing neuronal necrosis. Acute inflammatory response was evident at 12h and 24h, with immune cells infiltrating into the gray matter. Vascular permeability increased and the nerve cells in gray-white matter exhibited extensive damage and necrosis at 24h and 7 days after ASCI. MiR-9 expression in ASCI tissue was significantly lower than that in normal spinal cord tissue. Statistical analysis showed a significant decrease in miR-9 expression in all the ASCI groups, compared to the non-ASCI group. Results from real-time PCR analysis revealed that MCPIP1 expression in all the ASCI groups was significantly higher than the non-ASCI group, and MCPIP1 expressions gradually increased with times at 6h-24h after ASCI. ISH revealed the following results after ASCI (1) miR-9 and MCPIP1 mRNA expression mainly distributed in ventral horn motor neurons, (2) miR-9 expression was high at 7 day after ASCI and (3) in the non-ASCI group, MCPIP1 expression was high at 6h, 12h, 24h and 3 days.
MCPIP1 is significantly up-regulated after ASCI. The negative relationship between MCPIP1 and miR-9 suggest that MCPIP1 mRNA could be a target of miR-9 during ASCI. Thus, miR-9 is a marker for apoptosis in neurons, and an excellent therapeutic target for ASCI patients.
为了早期识别急性脊髓损伤(ASCI)的干预靶点,我们研究了大鼠ASCI模型中微小RNA-9(miR-9)和MCPIP1表达水平的变化。
将108只健康大鼠随机分为非ASCI组(n = 18)和五个ASCI组,分别代表ASCI后的6小时、12小时、24小时、3天和7天这几个实验时间点(每组n = 18)。采用苏木精-伊红(HE)染色评估ASCI损伤情况,运用定量实时聚合酶链反应(qRT-PCR)和原位杂交(ISH)检测miR-9和MCPIP1 mRNA表达。
HE染色结果显示,非ASCI组神经元形态正常,但ASCI后6小时脊髓组织出现神经元坏死。12小时和24小时出现明显急性炎症反应,免疫细胞浸润至灰质。ASCI后24小时和7天血管通透性增加,灰白质神经细胞出现广泛损伤和坏死。ASCI组织中miR-9表达明显低于正常脊髓组织。统计分析表明,与非ASCI组相比,所有ASCI组中miR-9表达均显著降低。实时PCR分析结果显示所有ASCI组中MCPIP1表达均明显高于非ASCI组且在ASCI后6小时至24小时MCPIP1表达随时间逐渐升高。ISH显示ASCI后结果如下:(1)miR-9和MCPIP1 mRNA表达主要分布在腹角运动神经元;(2)ASCI后7天miR-9表达较高;(3)在非ASCI组中,MCPIP1在6小时、12小时、24小时和3天表达较高。
ASCI后MCPIP1显著上调。MCPIP1与miR-9之间的负相关关系表明MCPIP1 mRNA可能是ASCI期间miR-9的作用靶点。因此,miR-9是神经元凋亡的标志物,也是ASCI患者的理想治疗靶点。