自发性嗜酸性粒细胞增多的MES大鼠Cyba变异和NADPH氧化酶活性降低的研究  

MUTATION IN Cyba AND DECREASE IN NADPH OXIDASE ACTIVITY IN MES RAT STRAIN WHICH SPONTANEOUSLY DEVELOPS EOSINOPHILIA

作　　者：李桂馨[1,2] 松本清司[3] 樋口京一 森政之[2] 蔡建辉[1] 

机构地区：[1]河北医科大学第二医院胃肠外科,河北石家庄050000 [2]日本信州大学医学系研究科加龄适应研究所加龄生物分野 [3]日本信州大学医学系实验动物中心

出　　处：《河北医科大学学报》2010年第9期1038-1040,共3页Journal of Hebei Medical University

基　　金：河北省教育厅留学人员科技活动项目择优资助项目

摘　　要：目的寻找导致MES(Matsumoto Eosinophilic Shinshu)大鼠嗜酸性粒细胞增多的致病基因和阐明发病机制。方法利用逆转录-聚合酶链反应,测序的方法,比较了MES大鼠和ACI大鼠位于19号染色体长臂末端的多个候选基因,并对其相应酶的活性进行了测定。结果在MES中,cyba基因转录mRNA在第4和第5外显子之间插入51个碱基,从而导致相应NADPH氧化酶的活性降低了49.86%。结论 cyba变异和NADPH氧化酶的活性降低可能与MES大鼠的嗜酸性粒细胞增多的发病机制有关。Objective To find causal gene and elucidate the mechanism （Matsumoto Eosinophilic Shinshu ） rat. Methods Examine the positional of eosinophilia in MES candidate genes were examined using RT - PCR and sequence , and then the activity of corresponding enzyme was mensured. Results cyba gene was inserted 51 - bp between exon 4 and exon 5 in MES rat. NADPH oxidase activity decreased 50% in MES rat. Conclusion Mutation in cyba and decrease in NADPH oxidase activity might be involved in the mechanism of eosinophilia in MES rat.

关 键 词：肺嗜酸粒细胞增多 NADPH氧化酶 大鼠 

分 类 号：R557.5[医药卫生—血液循环系统疾病]