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作 者:费鲜明[1] 王欢[1] 袁武峰[1] 蒋雷[1] 程茂良[2]
机构地区:[1]浙江省人民医院检验中心 [2]南京医科大学附属逸夫医院检验科
出 处:《中国临床药理学与治疗学》2017年第1期1-8,共8页Chinese Journal of Clinical Pharmacology and Therapeutics
基 金:国家自然科学基金资助项目(81301406);浙江省自然科学基金资助项目(LY17H080007;LQ13H190005)
摘 要:目的:观察木瓜蛋白酶对单核细胞-血小板聚集物(MPA)诱导的单核细胞分泌和黏附功能的抑制作用,并初步探讨其分子机制。方法:分离人外周血单核细胞和富血小板血浆(PRP),检测20 U/L木瓜蛋白酶不同作用方式下凝血酶和花生四烯酸(AA)诱导的MPA形成及肿瘤坏死因子-α(TNF-α)水平。将实验分为0(对照)、20、80U/L木瓜蛋白酶组,分别以ELISA、流式细胞术和显微镜检查测定木瓜蛋白酶与单核细胞共孵育后MPA诱导的单核细胞趋化蛋白-1(MCP-1)和组织因子(TF)释放、CD11b和CC趋化因子受体2(CCR2)表达水平以及单核细胞与人脐静脉内皮细胞黏附率,再以Western blot检测单核细胞Akt磷酸化(p-Akt)和环氧化酶-2(COX-2)表达水平。结果:20 U/L木瓜蛋白酶与单核细胞和血小板共孵育时显著降低凝血酶和AA诱导的MPA形成和TNF-α水平(P<0.01)。20 U/L木瓜蛋白酶组MCP-1和TF水平,CD11b和CCR2表达率,单核细胞与内皮细胞黏附率均显著低于对照组(P<0.01),80 U/L组对五者的抑制率显著高于20 U/L组(P<0.01)。木瓜蛋白酶显著抑制pAKT和COX-2表达,80 U/L组p-Akt和COX-2光密度比值显著低于20 U/L组(P<0.01)。结论:木瓜蛋白酶可通过抑制Akt磷酸化和COX-2表达途径而抑制MPA诱导单核细胞活化后的释放和黏附功能,从而可能有助于预防动脉粥样硬化。AIM: To observe the inhibitory effects of papain on monocyte secretory and adherent ability induced by monocyte-platelet aggregates (MPA), and to explore the preliminary molecular mechanisms. METHODS: Monocyte and platelet rich plasma were separated form human peripheral blood. Platelet were activated by thrombin and arachidonic acid, then mixed with monocyte in 20 U/L of papain, respectively, and levels of MPA and TNF-α were determined. The study was further di- vide into three groups : 0 (control) , 20, 80 U/L of papain group activated by 10 U/L thrombin, MCP- 1, tissue factor (TF), CDllb and CCR2 expres- sion, and adherent monocyte percent were measured by ELISA, flow cytometry, and microscopic exami- nation, respectively. Western blot analysis was used to detect the phosphorylated Akt and COX-2 expres- sion. RESULTS: In incubated with monocyte and platelet, 20 U/L of papain significantly decreased MPA formation and TNF-α levels induced by thrombin and araehidonic acid (P 〈0.01 ) . In 20 U/L of papain group, MCP-1, TF, CDllb and CCR2 expression levels, and adherent monocyte percent were significantly decreased compared with control group (P 〈 0.01 ). The inhibitory percent of the above- mentioned five markers were increased in 80 U/L group than that in 20 U/L group (P 〈 0. O1 ). Papain significantly inhibited Akt phosphorylation and COX-2 expression, there were lower photodensity ra- tios in 80 U/L group than that in 20 U/L group (P 〈 0.01 ). CONCLUSION: Papain may inhibit monocyte secretory and adherent ability induced by monocyte-platelet aggregates through the inhibition of Akt phosphorylation and COX-2 expression, and can be used to prevent atherosclerosis.
关 键 词:木瓜蛋白酶 单核细胞-血小板聚集物 单核细胞活化 AKT磷酸化 环氧化酶-2
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