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作 者:林丹[1] 王代友[1] 杨亦萍[1] 卿海云[1] 曹阳[1] 陈超梅[1] 沈洁[1] 欧健波[1]
机构地区:[1]广西医科大学口腔医学院口腔颌面外科,广西南宁530021
出 处:《临床口腔医学杂志》2011年第12期721-724,共4页Journal of Clinical Stomatology
基 金:国家自然科学基金项目(30960420);广西医疗卫生重点科研课题(桂卫重2010082)
摘 要:目的:研究大鼠涎腺放射损伤模型中NBS1基因的表达,初步探讨其在放射性涎腺上皮细胞损伤修复中的调控作用。方法:放射组40只大鼠以60Coγ射线分次照射,每次3GY,隔天1次,共5次,累积剂量分别为3、6、9、12、15 GY,对照组40只大鼠同期进行麻醉。照射后2~4 h,收集大鼠腮腺,颌下腺。应用苏木素-伊红染色(HE)和透射电镜观察涎腺组织的显微和超微结构变化;应用逆转录聚合酶链技术(RT-PCR)检测腮腺、颌下腺NBS1mRNA的表达情况。结果:腮腺较颌下腺组织损伤严重;放射组和正常组比较,腮腺放射剂量9 GY组起,颌下腺于12 GY组起,NBS1mRNA表达水平减少(P<0.05)。结论:大鼠涎腺放射损伤模型建立成功,NBS1可能参与涎腺放射损伤修复。Objective: To investigate the expression of NBS1 genes in the radiation-injured model of salivary gland in rats, and preliminary explore the irradiated injury repair mechanism of NBS1 in salivary gland. Method: The rats were randomly divided into two groups, the irradiated rats (n=40) were fractionated exposed to a dose of 3Gy ^60Co γ-rays, given two days time , leading to an calculated dose of 3,6, 9, 12, 15GY; The sham-irradiated controls (n=40) were anesthetized in parallel with the irradiated rats but not irradiated. After irradiation in two to four hours,the rats were sacrificed, the histomorphological changes were observed by HE staining;the ultrastructural changes were observed by transmission electron microscopy; RT-PCR were used to detect the NBSlexpression. Result:The organization were damaged even more serious in parotid gland than in submandibular gland; Compared with the controls,with the groups of dose above 9Gy in parotid gland and the dose above 12GY in the submandibular gland, the expression of NBS1 mRNA were reduced (P 〈 0.05).Conclusions:The model of irradiated injury salivary gland was successfully constructed, NBSI might be involved in salivary gland irradiated injury repair.
关 键 词:NBS1:MRN(MRE11-RAD50-NBS1)复合物 DNA双链断裂(DSB) 涎腺上皮细胞 放射性损伤修复
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