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作 者:倪志宇[1] 董玫[1] 徐之璐[1] 文迪[1] 李淑瑾[1] 丛斌[1]
机构地区:[1]河北医科大学基础医学院法医学系河北省法医学重点实验室,河北石家庄050017
出 处:《中国药理学通报》2011年第11期1578-1582,共5页Chinese Pharmacological Bulletin
基 金:国家自然科学基金资助项目(No30770839);河北省自然科学基金资助项目(NoC2008001045);河北省科技厅博士基金资助项目(No06547008D)
摘 要:目的研究八肽胆囊收缩素(CCK-8)对LPS诱导RAW264.7细胞IL-6表达的影响及相关机制。方法用ELISA及RT-PCR法检测RAW264.7细胞IL-6蛋白及mR-NA表达;用EMSA方法检测RAW264.7细胞AP-1 DNA结合活性。结果①LPS可时间依赖性的诱导RAW264.7细胞IL-6蛋白及mRNA表达;②10-10 mol.L-1 CCK-8对LPS诱导的RAW264.7细胞IL-6表达无明显影响;10-8、10-6 mol.L-1 CCK-8浓度依赖性地抑制了LPS诱导的RAW264.7细胞IL-6表达;③10-10 mol.L-1 CCK-8未影响LPS诱导的AP-1活性,10-8、10-6 mol.L-1 CCK-8浓度依赖性地抑制了LPS诱导的AP-1活性。结论 CCK-8通过抑制AP-1 DNA结合活性而抑制了LPS诱导的RAW264.7细胞IL-6表达,这可能是CCK-8发挥抗炎作用的信号转导机制之一。Aim To explore the inhibitory effects of cholecystokinin octapeptide(CCK-8) on LPS-induced IL-6 expression in RAW264.7 cells and its mechanism.Methods IL-6 protein and mRNA expression in LPS-induced RAW264.7 cells were assayed by ELISA and RT-PCR,and AP-1 DNA-binding activity was tested by EMSA.Results ① The expression of IL-6 protein and mRNA were induced by LPS in a time-dependent manner in RAW264.7 cells.② 10-10 mol·L-1 CCK-8 had no effect on LPS-induced IL-6 expression in RAW264.7 cells;while 10-8,10-6 mol·L-1 CCK-8 concentration-dependently inhibited LPS-induced IL-6 expression.③ CCK-8 had no effect on LPS-induced AP-1 activation in RAW264.7 cells,while 10-8,10-6 mol·L-1 CCK-8 inhibited LPS-induced AP-1 activation in a concentration-dependent manner.Conclusion CCK-8 inhibits LPS-induced IL-6 expression in RAW264.7 cells via inhibiting AP-1 DNA-binding activity,which may be one of the mechanisms of CCK-8 anti-inflammatory effects.
关 键 词:胆囊收缩素 脂多糖 白细胞介素-6 激活蛋白1 RAW264.7细胞 炎症
分 类 号:R329.25[医药卫生—人体解剖和组织胚胎学] R392.12[医药卫生—基础医学]
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