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机构地区:[1]蚌埠医学院病原生物学教研室安徽省感染与免疫重点实验室,蚌埠233030
出 处:《中国人兽共患病学报》2010年第3期197-200,共4页Chinese Journal of Zoonoses
基 金:安徽省高校省级自然科学研究计划项目(KJ2008B320);安徽省省级重点实验室重点科研项目(2004sys008);蚌埠医学院科研项目(BY0901)联合资助
摘 要:目的探讨结核分枝杆菌19kD脂蛋白(MtbP19)对单核巨噬细胞功能及表型的影响。方法以10μg/mLMtbP19作用于拂波醇酯(PMA)分化的THP-1细胞,CO2孵箱孵育,酶联免疫吸附法(ELISA)检测不同时间巨噬细胞TNF-α和IL-6的分泌水平;对巨噬细胞表型分子HLA-DR进行荧光抗体染色,流式细胞术分析P19对巨噬细胞表型的影响;流式细胞术及光学显微镜研究MtbP19对巨噬细胞吞噬活性的影响。结果P19能够诱导巨噬细胞TNF-α和IL-6分泌水平的增加,呈时间依赖关系;经P19刺激的巨噬细胞HLA-DR表达增强,平均荧光强度(MFI)为(54.3±3.4)%,与BSA对照组(34.3±3.6)%比较P<0.05;P19能增强巨噬细胞的吞噬活性。结论MtbP19能诱导巨噬细胞活化,在感染过程中可能具有一定的抗结核保护作用。To observe the influence of Mycobacterium tuberculosis 19-kDa lipoprotein(Mtb P19) on function and phenotype of macrophage,the Mtb P19 was prepared from cultured Mtb H37Ra and the phorbol myristate acetate-differentiated THP-1 cells were incubated with P19 at the concentration of 10 μg/mL with 5% CO2 at 37℃ for up to 48 hours.Supernatants were collected for TNF-α and IL-6 detection by ELISA,then the phenotype fluorescent antibodies were stained to analyze HLA-DR expression changes between control group and experimental group.Flow cytometry and microscopy was used to assay the phagocytosis in macrophages stimulated by Mtb P19.IL-6 and TNF-α in collected supernatants were detected.Results indicated that both were found significant increases and their phagocytosis were enhanced.Comparing to the control group,the mean fluorescence intensity showed a significant increase 24hs after stimulation.It presents that Mtb P19 could be able to induce macrophages activation,and it would be significantly important for protection during infection period.
关 键 词:结核分枝杆菌P19 THP-1细胞 细胞因子 表型分子 吞噬
分 类 号:R378.9[医药卫生—病原生物学]
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