摘要
目的:研究小鼠病毒性心肌炎(VMC)模型中白细胞介素(IL)-27基因和蛋白的表达,探究其在VMC发病中的作用及意义。方法:VMC组用柯萨奇病毒B3(CVB3)感染Balb/c小鼠建立VMC模型,注射100TCID 50病毒液0.1ml;对照组注射等量磷酸盐缓冲液(PBS)。在注射后的第0、1、2、3、4和6周应用逆转录-聚合酶链反应检测两组小鼠心肌组织中IL-27亚基p28及EBI3的mRNA表达,酶联免疫双夹心抗体法检测血清中IL-27蛋白的表达。结果:与对照组比较,VMC组小鼠心肌组织中IL-27p28mRNA水平自第1周开始升高,第2周时达峰值,并至少维持至第6周(均P〈0.05);VMC组第1~6周各时点血清IL-27蛋白均明显高于对照组(均P〈0.05);与对照组同时点比较,VMC组各时点小鼠心肌组织中IL-27EBI3mRNA差异均无统计学意义。结论:IL-27在VMC小鼠中高表达,提示IL-27可能参与VMC的发病机制。
Objective:To investigate the expression of interleukin-27(IL-27)in the coxsackievirus B3-induced mice viral myocarditis(VMC).Method:BALB/c mice were intraperitoneally infected with CVB 3for establishing VMCmodels.Control mice were treated with phosphate-buffered saline(PBS).On 0,1,2,3,4,6week after injection,expressions of serum IL-27were analyzed by enzyme linked immosorbent assay(ELISA).Productions of cardiac IL-27p28and EBI3mRNA were measured by real time-polymerase chain reaction(RT-PCR).Result: Levels of cardiac IL-27p28mRNA obviously increased in VMC mice on week 1after infection,peaked on week 2, and highly persisted to at least week 6(all P0.05).Compared with control group,serum IL-27protein was higher in VMC group from week 1to week 6(all P0.05).There was no significant difference production of cardiac IL-27EBI3mRNA was found between VMC and control group throughout the course of the experiment.Conclusion:The increased levels of IL-27may play an important role in the pathogenesis of CVB3-induced mice VMC.
出处
《临床心血管病杂志》
CAS
CSCD
北大核心
2014年第2期110-113,共4页
Journal of Clinical Cardiology
基金
国家自然科学基金资助项目(No:81160032)