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作 者:庞伟[1] 王成彬[2] PANG Wei WANG Cheng-bin(Department of Clinical laboratory, Affiliated Hospital of Logistics University of PAP, Tianjin 300162,China)
机构地区:[1]武警后勤学院附属医院检验科,天津300162 [2]解放军总医院临检科,北京100853
出 处:《武警后勤学院学报(医学版)》2017年第6期461-465,共5页Journal of Logistics University of PAP(Medical Sciences)
基 金:国家自然科学基金项目(30873419);武警后勤学院院级课题项目(FYM201608)
摘 要:【目的】观察支气管上皮细胞(BEAS-2B细胞)和嗜中性粒细胞(Neutrophils细胞)接触共培养体系中基质金属蛋白酶组织抑制剂-2(tissue inhibitors of metalloproteinases-2,TIMP-2)合成,探讨不同剂量葛根素对共培养体系TIMP-2的抑制作用。【方法】应用蛋白芯片筛查不同培养体系炎性细胞因子表达;应用ELISA方法定量测量TIMP-2浓度;应用Real-time PCR方法检测TIMP-2基因表达。【结果】BEAS-2B细胞和Neutrophils细胞联合培养上清液中TIMP-2浓度升高,基因表达水平明显上调(P<0.05)。经葛根素干预可显著抑制两种细胞联合培养TIMP-2浓度及基因表达(P<0.05)。【结论】Neutrophils细胞与BEAS-2B细胞联合培养可显著增加细胞培养上清液中炎性细胞因子TIMP-2浓度,上调BEAS-2B细胞中TIMP-2基因表达;葛根素可下调TIMP-2浓度及表达。【Objective】To observe the expression of TIMP-2 in co-cultured BEAS-2B cells and neutrophils, and explore the inhibitory effect of different doses of puerarin on TIMP-2 in the co-cultured system.【Methods】The expression of inflammatory cytokines in different culture systems was detected by protein chip technology. The concentrations of TIMP-2 were quantified by enzyme linked immunosorbent assay(ELISA). The gene expression of TIMP-2 was determined by real-time quantitative polymerase chain reaction(Real-time q PCR).【Results】The concentration of TIMP-2 in the supernatant of co-cultured BEAS-2B cells and neutrophils increased(P〈0.05), and the gene expression of TIMP-2 was significantly up-regulated(P〈0.05). Puerarin could significantly decrease the concentration of TIMP-2 and obviously downregulate the gene expression of TIMP-2 in co-cultured BEAS-2B cells and neutrophils(P〈0.05).【Conclusion】In the co-cultured neutrophils and BEAS-2B cells, the concentration of TIMP-2 can significantly increase.The gene expression of TIMP-2 can be upregulated in BEAS-2B cells. Puerarin can decrease the concentration of TIMP-2 and downregulate its expression.
关 键 词:支气管上皮细胞 抑制 基质金属蛋白酶组织抑制剂-2
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