LPS对大鼠雪旺氏细胞iNOS表达的影响  被引量:8

Effect of LPS on inducible nitric oxide synthase in rat Schwann cells

在线阅读下载全文

作  者:王海波[1] 秦永伟[2] 程纯[2] 牛淑琼[1] 周丹[2] 沈爱国[1] 

机构地区:[1]南通大学神经再生重点实验室,南通226001 [2]南通大学医学院微生物和免疫学教研室,南通226001

出  处:《中国免疫学杂志》2007年第9期815-818,共4页Chinese Journal of Immunology

基  金:国家自然科学基金(No30300099);江苏省自然科学基金(BK2003035);江苏省高校自然科学研究项目(KJB320114);江苏省社会发展科技指导性计划项目(BS2004526);江苏省"六大人才高峰"第二批项目资助

摘  要:目的:探讨内毒素脂多糖(Lipopolysaccharide,LPS)对大鼠雪旺氏细胞(Schwann cells,Scs)诱导型一氧化氮合酶(Inducible nitric-oxide synthase,iNOS)基因表达及一氧化氮(Nitric oxide,NO)生成的影响。方法:用不同浓度(1、10、100μg/ml)和同一浓度不同时间(1、2、4、6小时)的LPS刺激雪旺氏细胞,分别用RT-PCR和亚硝酸盐含量测定观察细胞iNOS mRNA的表达量和细胞培养液中亚硝酸盐的水平,同时用免疫荧光细胞化学染色检测iNOS的细胞定位。结果:用LPS10μg/ml刺激2小时后,iNOS mRNA的表达增加,4小时表达活性最高。细胞上清中的亚硝酸盐含量高峰在6小时。免疫细胞化学证明LPS诱导雪旺氏细胞iNOS的表达定位在胞浆。结论:LPS可在转录水平上诱导雪旺氏细胞iNOS mRNA表达,促进NO的合成,提示雪旺氏细胞在周围神经系统炎症过程中可能发挥免疫调节作用。Objective:To explore the effect of lipopolysaccharide (LPS) on the expression of inducible nitric oxide synthase (iNOS) gene and nitric oxide (NO) production in rat Schwann cells. Metbods:Schwann cells were treated with LPS at different concentration (1,10,100μg/ml) and at the same concentration (10 μg/ml) for different time (1,2,4,6 h). With RT-PCR and measurement of nitrite, the expression of iNOS gene and the level of nitrite in the culture medium were observed . Intracellular location of iNOS was detected under confocal microscope. Results:iNOS mRNA increased after 2 h exposure to LPS ( 10 μg/ml ) , and peaked at 4 h. The peak of nitrite in the supernatant was at 6 h. Immunocytochemical staining indicated the expression of iNOS was located in the cytoplasm following LPS induction. Conclusion: Bacterial causative agent-LPS could induce the expression of iNOS mRNA in rat Schwann cells at transcription level and lead to the synthesis of NO. It was showed that Schwann cells may play a role for immunoregulation after inflammation in the peripheral nerve system.

关 键 词:脂多糖 雪旺氏细胞 诱导型一氧化氮合酶 

分 类 号:R392.11[医药卫生—免疫学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象