摘要
目的探讨CD2 8/CTLA 4,B7在小鼠实验性变态反应言神经炎 (EAN )中的变化规律及对发病的影响。方法于小鼠双后肢足垫皮下注射兔坐骨神经匀浆 ,建立EAN模型 ,用免疫组化观察外周淋巴细胞CD2 8,CTLA 4,B7 1和B7 2蛋白的表达 ;用RT PCR检测外周淋巴细胞B7 1和B7 2mRNA的表达。结果B7 1蛋白和mR NA及CTLA 4蛋白从潜伏期至发病高峰呈递增趋势 ,而B7 2蛋白和mRNA及CD2 8蛋白从潜伏期至发病初期明显增高 ,至发病高峰又下降。结论CD2 8/CTLA 4,B7与EAN的发病密切相关。B7 2可能与EAN的始发有关 ,而B7 1与EAN的进展及维持关系更密切。
ObjectiveTo investigate the changing rules of CD28,CTLA 4,B7 1 and B7 2 as well as their effects on the onset of disease in experimental allergic neuritis(EAN).MethodsEAN models were established on mice by subcutaneous injection of homogenate prepared from rabbit sciatic nerves.The expression of CD28,CTLA 4,B7 1 and B7 2 proteins in lymphocytes of peripheral blood was examined with immunohistochemistry,and that of B7 1 and B7 2 mRNA with RT PCR dynamically on day 14(incubation period),day 18(primary period)and day 22(peak of disease)after mice immunization.ResultsExpression of B7 1 protein/mRNA and CTLA 4 protein increased progressively from incubation period to the peak of disease,whereas that of B7 2 protein/mRNA and CD28 protein increased markedly from incubation period to the early stage of disease,then decreased during the peak of EAN.ConclusionsThe increased expression of CD28/CTLA 4,B7 is closely related with the occurrence of EAN,while B7 2 is considered to be involved in the initiation of the disease and B7 1 in its progress and persistence.
出处
《湖南医学》
2000年第2期86-88,共3页
Hunan Medical Journal
基金
国家自然科学基金课题!(No .39870 90 9)
湖南省科委基金课题 !(97JJY2021)
关键词
神经炎
实验性变应性
EAN
CD28/CTLA-4
neuritis
experimental allergic
minor lymphocyte stimulatory antigens
polymerase chain reaction
disease models
animals
mice